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Article

Molecular Cloning of the B4GALNT2 Gene and Its Single Nucleotide Polymorphisms Association with Litter Size in Small Tail Han Sheep

by
Xiaofei Guo
1,2,†,
Xiangyu Wang
1,†,
Benmeng Liang
1,
Ran Di
1,
Qiuyue Liu
1,
Wenping Hu
1,
Xiaoyun He
1,
Jinlong Zhang
2,
Xiaosheng Zhang
2 and
Mingxing Chu
1,*
1
Key Laboratory of Animal Genetics and Breeding and Reproduction of Ministry of Agriculture, Institute of Animal Science, Chinese Academy of Agricultural Sciences, Beijing 100193, China
2
Tianjin Institute of Animal Sciences, Tianjin 300381, China
*
Author to whom correspondence should be addressed.
†
These authors contributed equally to this study.
Animals 2018, 8(10), 160; https://doi.org/10.3390/ani8100160
Submission received: 1 August 2018 / Revised: 1 September 2018 / Accepted: 15 September 2018 / Published: 20 September 2018
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Abstract

:

Simple Summary

In French Lacaune sheep, the B4GALNT2 (beta-1, 4-N-acetyl-galactosaminyl transferase 2) gene was considered as the potential gene for a FecL (mutation), which regulates the ovine ovulation rate. Three specific mutation sites linked with the FecL mutation have not been previously found in 11 sheep breeds. However, two mutations of g.36946470C > T and g.36933082C > T in the exon of B4GALNT2 were found to have had a significant effect on the litter size in the first parity for Small Tail Han (STH) Sheep (p < 0.05). B4GALNT2, which is mainly expressed in ovine ovary, also plays an important role in sheep reproduction. Furthermore, we discovered two transcription start sites (TSS) of B4GALNT2 in its 5′-flanking region in ovine granule cells in vitro.

Abstract

A new fecundity gene named the FecL (mutation), which regulates the ovulation rate, was discovered in French Lacaune sheep. The B4GALNT2 (beta-1, 4-N-acetyl-galactosaminyl transferase 2) gene was considered as the potential FecL mutation gene. This study explores whether the effect of the FecL mutation exists in other sheep breeds, and the features of the B4GALNT2 gene in terms of the molecular structure and its expression profile. Using Sanger sequencing, we found that high and low fecundity breeds from among 11 measured sheep breeds all had no variation in the three specific mutation sites, which were linked with the FecL mutation. However, two mutations of g.36946470C > T and g.36933082C > T in the exon of B4GALNT2 had a significant effect on litter size in the first parity for Small Tail Han (STH) Sheep (p < 0.05). Two transcription start sites (TSS) of B4GALNT2 in its 5′-flanking region were discovered in ovine granule cells in vitro, through the RACE (Rapid amplification of cDNA ends) method. Except for in the kidney and oviduct, no significant difference in expression levels had been found between STH sheep and Tan sheep breeds. The B4GALNT2 gene, as a candidate for FecL, may have a relationship with the differences in litter size in STH sheep. B4GALNT2 is mainly expressed in the ovine ovary, which also suggests that B4GALNT2 plays an important role in sheep reproduction.

1. Introduction

On account of annual mutton production being determined by annual sheep slaughter rates and individual average meat yield, high levels of ewe reproduction are equally important to superior carcass traits in meat sheep production. However, reproduction traits with relatively low heritability that are generally not expressed until puberty, and are normally recorded only in females, resulting in the genetic improvement of reproduction in sheep being a challenge [1,2]. Litter size and the ovulation rate (OR), involved in reproduction traits, could be regulated by the action of single genes with major effects, called fecundity (Fec) genes [3,4]. For the last three decades, geneticists have created informative families for segregation studies and fine mapped some of the Fec genes that affect ovine litter size and OR [5]. To date, the most efficient of the three Fec genes, Bone Morphogenetic Protein-15 (BMP15) [6,7,8,9,10], Growth and Differentiation Factor-9 (GDF9) [10,11,12,13], and Bone Morphogenetic Protein receptor type-1B (BMPR1B) (the FecB gene [7,8,14,15,16]) have all belonged to the Bone Morphogenetic Protein (BMP) system [5]. Nevertheless, a newly founded FecL gene named beta-1, 4-N-acetyl-galactosaminyl transferase 2 (B4GALNT2), encoding for a glycosylation enzyme, which was not related to the BMP family, recently attracted the attention of researchers [17].
In the meat strain of the Lacaune sheep breed in France, large variations in litter size and OR have been observed, and at least two major genes could explain this variation. One was X-linked—namely Fec, and the second was autosomal—namely FecL [6,18,19,20]. Similarly to the FecB mutation, the influence of the FecL mutation on OR was also additive, with extra ovulations increasing by approximately 1.5 for one copy and by 3.0 for two copies [4,17,18,19]. In 2009, Drouilhet et al. reported that a unique haplotype was associated with the FecL mutation, and they had reached the conclusion that the DLX3:c. * 803A > G Single Nucleotide Polymorphisms (SNP) provided accurate classification of 99.5% of sheep as carriers or non-carriers of the FecL mutation [4]. In 2013, consideration of two mutations (the SNP g.36938224T > A mutation, localized in the intron 7 of B4GALNT2, and the SNP g.37034573A > G mutation, localized in the intergenic sequence between B4GALNT2 and EZR) that were closely associated with the FecL mutation appeared to suggest that B4GALNT2 appeared as the best positional and expressional candidate for the FecL gene [17]. The B4GALNT2 gene in humans, encoding for the glycosylation enzyme beta-1, 4-N-acetyl-galactosaminyl transferase 2, was involved in the pathway of protein glycosylation or modification [21].
The FecB gene was found in Booroola Merino sheep and regarded as the first major gene for prolificacy, and was also identified in various other sheep breeds [7,22,23,24,25]. However, whether the effects of the FecL mutation, which was found in the Lacaune sheep breed, also exists in other sheep breeds remains unknown. In the present study, three specific linked marker mutations (DLX3:c. * 803A > G, g.36938224T > A, g.37034573A > G) for FecL were detected using the sequencing method in 11 sheep breeds (Small Tail Han (STH) sheep, Hu sheep, Cele Black sheep, Tan sheep, White Suffolk sheep, Black Suffolk sheep, East Friesian sheep, Dorset sheep, Mutton Merino sheep, Dorper sheep, and Corriedale sheep). Based on previous data from the whole-genome sequencing (WGS) performed by our research team, seven SNPs of the B4GALNT2 gene were detected in 99 experimental sheep [26,27]; we explored the frequency of the seven SNPs in STH sheep and studied their relationship with litter size. Then, the B4GALNT2 transcripts were cloned, and the corresponding protein sequence and its bioinformatics were predicted in the research. The tissue expression profiles of B4GALNT2 in STH sheep and Tan sheep were implement, to explore the gene expression difference between high and low fecundity breeds. The data obtained, and the results of these analyses, will help us to understand the effect of the sheep B4GALNT2 gene on sheep reproductive traits.

2. Materials and Methods

2.1. Experimental Animals and Sample Collection

High and low fecundity breeds were selected to detect the mutations with linkage with FecL. Jugular blood samples from 88 STH sheep (recorded with data of the litter size) and varied fecundity of different sheep breeds (STH sheep, Hu sheep, Cele Black sheep, Tan sheep, White Suffolk sheep, Black Suffolk sheep, East Friesian sheep, Dorset sheep, Mutton Merino, Dorper sheep, and Corriedale sheep). Samples from a total of 30 ewes, from these breeds, were collected and stored at −20 °C for DNA extraction. Three female STH sheep and three female Tan sheep, each aged two years old, were purchased from purebred herds from the same farm in the Ningxia province. The six selected sheep were healthy, similar in weight, and fed in an indoor setting under similar conditions of room temperature, illumination, feeding system, and nutrition level. The six female sheep were slaughtered in autumn when they accepted the teasing behavior for the advent of oestrum. The tissues of the heart, liver, spleen, lung, kidney, oviduct, uterine horn, uterine body, muscle, cerebellum, hypothalamus, pituitary, and ovary in estrus from the six sheep were collected and frozen in liquid nitrogen instantly, then stored at −80 °C for RNA extraction. All the experimental procedures mentioned in the present study were approved by the Science Research Department (in charge of animal welfare issues) of the Institute of Animal Sciences, Chinese Academy of Agricultural Sciences (IAS-CAAS) (Beijing, China). Ethical approval on animal survival was given by the animal ethics committee of IAS-CAAS (No. IASCAAS-AE-03, 12 December 2016).

2.2. Genotyping the Known SNPs Linked with the FecL Mutation

Genomic DNA were extracted from the blood samples with a Blood DNA kit (TIANGEN Biotech Co., Ltd., Beijing, China). The primers for the detection of two mutations (the mutation g.36938224T > A, localized in the intron 7 of B4GALNT2, and the mutation g.37034573A > G, localized in the intergenic sequence between B4GALNT2 and EZR) and one linked marker mutation (DLX3:c. * 803A > G SNP) were designed based on the reference genome of ovis aries Oar_3.1 (Supplementary File 1). In this study, a total of 11 sheep breeds (STH sheep, Hu sheep, Cele Black sheep, Tan sheep, White Suffolk sheep, Black Suffolk sheep, East Friesian sheep, Dorset sheep, Mutton Merino sheep, Dorper sheep, and Corriedale sheep) of different lambing rates, with 30 individuals of each breeds, were utilized for detection by the Sanger sequencing method to explore the polymorphism of the three specific mutations, as stated above.

2.3. Genotyping the Seven SNPs of the B4GALNT2 Gene Mentioned in WGS

A total of 99 experimental sheep from 10 breeds were used for WGS in our previous study, and seven SNPs in exons for the B4GALNT2 gene were found. The primers for the seven SNPs (g.36971115C > T, g.36946470C > T, g.36946465G > A, g.36942215T > C, g.36933082C > T, g.36933070G > A, g.36930089T > G) detected were also designed based on the reference genome of ovis aries Oar_3.1 (Supplementary File 1). Then, the polymorphisms of the seven SNPs for the B4GALNT2 gene were also detected by the Sanger sequencing method in 88 STH sheep, which was recorded along with data of litter size. Finally, the relationship between the genotype frequency of the seven SNPs and litter size in STH sheep was analyzed by a chi-square test. The Linkage Disequilibrium (LD) pattern for the SNPs that were genotyped was plotted using Haploview (Version 4.2).

2.4. Amplification Full Length of Ovine B4GALNT2 Transcripts

Total RNA was extracted from each tissue using TRIzol Reagent (Invitrogen Inc., Carlsbad, CA, USA). cDNA for the tissue expression profile was synthesized using a PrimeScript® RT Reagent Kit (Takara Bio Inc., Dalian, China) according to the manufacturer’s instructions. Total RNA from granulosa cells, which were cultured in vitro, was extracted for RACE (rapid amplification of cDNA ends)-Ready cDNA following the user manual of SMARTer® RACE5′/3′ (Clontech Laboratories, Inc., Mountain View, CA, USA). The procedure of granulosa cells culture was as follows: Granulosa cells were aspirated from visible follicles (>3.0 mm in diameter), and separated from the follicular followed by washing with sterile Dulbecco’s Modified Eagle’s Medium (DMEM). The cells were evenly plated onto cell culture plates in the same medium supplemented with 15% fetal bovine serum and 1% penicillin streptomycin solution, and then incubated at 37 °C under 5% CO2 in humidified air.
There are several predicted transcripts for B4GALNT2 gene in NCBI. In order to analyze the properties of B4GALNT2 protein subsequently, we should perform the cDNA clone to obtain the real and complete ovine B4GALNT2 transcript sequence. The primers for the cDNA synthesis, shown in Supplementary File 1, were designed according to the sequence of beta-1, 4-N-acetyl-galactosaminyl transferase 2 (B4GALNT2), transcript variant X7, mRNA, XM_012185950. P9–P14 were used for cDNA amplification and assembly (Supplementary File 1). After the partial CDS sequence had been cloned, the 3’RACE GSP inner primer (3′GIP), 3′RACE GSP outer primer (3′GOP), and 5′RACE GSP primers (5′GP1-5′GP2) were designed to obtain the 3′UTR and 5′UTR of B4GALNT2 (Supplementary File 1). The procedure of touchdown Polymerase Chain Reaction (PCR) is as follows: Initial denaturation for 5 min at 94 °C, followed by 10 cycles of denaturation for 30 s at 94 °C, annealing for 30 s at 72 °C (with a decrease of 0.4 °C per cycle), and extension for 3 min at 72 °C, another 30 cycles of 30 s at 94 °C, 30 s at 68 °C, and 3 min at 72 °C, with a final extension for 8 min at 72 °C. The PCR products were purified using a DNA Purification Kit (TIANGEN Biotech Co., Ltd., Beijing, China), and were cloned into the pMDTM18-T Vector (Takara Bio Inc., Dalian, China), then transformed into competent cells DH5α (Takara Bio Inc., Dalian, China) for ultimate clone sequencing.

2.5. Bioinformatics Analysis

The DNA star was used to predict the B4GALNT2 gene open reading frame (ORF) and amino acid sequence. According to the report of Wilkins et al., the fundamental characteristics of predicted B4GALNT2 proteins were forecasted by ProtParam (http://www.expasy.org/tools/protparam.html) [28]. The transmembrane domains were speculated by TMHMM (http://www.cbs.dtu.dk/services/TMHMM-2.0). The subcellular localization of the B4GALNT2 protein was assessed by TargetP (http://www.cbs.dtu.dk/services/TargetP/) and the Uniprot database (http://www.uniprot.org/). Potential disulphide bonds, N-glycosylation sites, and phosphorylation sites were predicted using the SCRATCH protein predictor (http://scratch.proteomics.ics.uci.edu/), NetNGlyc (http://www.cbs.dtu.dk/services/NetNGlyc/), and NetPhos (http://www.cbs.dtu.dk/services/NetPhos/), respectively. The hydrophilicity and average flexibility index of ovine B4GALNT2 amino acid sequences were analyzed by ProtScale (http://web.expasy.org/protscale/). SMART (Simple Molecular Architecture Reasearch Tool) (http://smart.embl-heidelberg.de/) and MEME (Multiple Em for Motif Elicitation) (http://meme-suite.org/tools/meme) were used to forecast the conserved domain of B4GALNT2. The secondary and tertiary structures of ovine B4GALNT2 were predicted by PSIPRED (http://bioinf.cs.ucl.ac.uk/psipred) and Phyre2 (http://www.sbg.bio.ic.ac.uk/phyre2/html/page. cgi?id=index), respectively. NCBI Blast (https://blast.ncbi.nlm.nih.gov/Blast.cgi) and MEGA software (version 6.0) were used to implement multiple alignments and molecular phylogenetic tree construction.

2.6. B4GALNT2 Expression Profile in STH Sheep and Tan Sheep

P15 in Supplementary File 1 was used to detect the expression profile of B4GALNT2 in two sheep breeds by qRT-PCR (Quantitative Real Time Polymerase Chain Reaction). The housekeeping gene β-actin (P16) was adopted as the internal control in this study (Supplementary File 1). A SYBR® Premix Ex Taq™ kit (Takara Bio Inc., Dalian, China) for the qRT-PCR reaction was used in the LightCycler® 480 Real-Time PCR system (Roche Applied Science, Mannheim, Germany) to quantify the expression levels of B4GALNT2 in each tissue. Each 20 μL PCR reaction system contained 10 μL SYBR® Premix Ex TaqTM II (Tli RNaseH Plus, 2×), 2 μL cDNA (ddH2O used as a blank control), 0.8 μL forward primer, and 0.8 μL reverse primer of the working solution concentration, and the rest of the volume was supplemented by ddH2O. The program of the qRT-PCR reaction is as follows: Denaturation at 95 °C for 3 min, followed by 40 cycles of 10 s at 95 °C, and 10 s at 60 °C, then the melting curves were collected. All the reactions were performed in triplicate. β-actin was used as the internal control, and the method of 2−ΔΔCT was adopted to calculate the relative expression level of mRNA [29]. Analysis of Variance was performed for the significance test of expression analysis by SAS 8.0 software (SAS Institute Inc., Cary, NC, USA). Chi-square test was adopted to analyze the significant difference of litter size among the three genotype groups in each of the parities.

3. Results

3.1. Genotype Frequencies of Three Specific SNPs for the FecL Mutation

Three kinds of DNA fragments, which were used to detect the three SNPs closely associated with the FecL mutation sites (the mutation g.36938224T > A, localized in the intron 7 of B4GALNT2; the mutation g.37034573A > G, localized in the intergenic sequence between B4GALNT2 and EZR; and the mutation DLX3:c. * 803A > G), were successfully amplified (Figure 1a–c). Three kinds of amplification fragment sizes were consistent with the anticipated lengths, which could be directly genotyped by the Sanger sequencing method. The results showed that, of the 11 measured sheep breeds, the consistency of high fecundity breeds (STH sheep, Hu sheep, Cele Black sheep) with low fecundity breeds (Tan sheep, White Suffolk sheep, Black Suffolk sheep, East Friesian sheep, Dorset sheep, Mutton Merino sheep, Dorper sheep, and Corriedale sheep) all had no variation in the three specific mutation sites (Figure 1d–f).

3.2. Genotype Frequencies for the Seven SNPs of the B4GALNT2 Gene in STH Sheep

Because none of the three known SNPs were identified in the eleven breeds, we looked up the data of WGS to search for other SNPs (sense mutation) in candidate gene (B4GALNT2). Fortunately, seven SNPs in B4GALNT2 were found in the data of WGS. Combine with litter size data in STH sheep breed, the relationship between litter size and the unmentioned seven SNPs were studied in STH sheep. Seven SNPs in the exons of the ovine B4GALNT2 gene discovered through WGS are listed in Table 1. Six of them had been found before and released in dbSNP with variant ID, and only the SNP in the position of g.36946465 was a new mutation. The four SNPs of g.36971115C > T, g.36946470C > T, g.36933082C > T and g.36930089T > G were detected in 88 STH ewes, which were recorded along with data of litter size. The CDS position of them were C205T, C482T, C865T and T1302G, respectively (Table 2).

3.3. SNPs of B4GALNT2 Associated with Litter Size in STH Sheep

For the four SNPs detected in STH sheep, the result of the chi-square test in Table 3 indicated that the genotype of g.36946470C > T and g.36933082C > T had a significant effect on litter size in the first parity (p < 0.05). In g.36946470C > T site, mean litter size of the first parity for CC and CT were 2.17 ± 0.11 and 2.32 ± 0.18, which were significantly higher than 1.25 ± 0.25 for the TT genotype (p < 0.05). However, the litter size between CC and CT showed no significant difference (p > 0.05). In the g.36933082C > T site, no TT genotype was found, and the mean litter size of the first parity for CC was 2.08 ± 0.09, which was significantly lower than 2.59 ± 0.24 for CT genotype (p < 0.05). In STH sheep, a haplotype block of B4GALNT2 was identified: The block with the SNPs g.36971115C > T, g.36946470C > T, g.36933082C > T and g.36930089T > G (Supplementary File 2). The site of g.36971115C > T and g.36930089T > G possessed a significant linkage disequilibrium with D′ > 0.8 and r2 > 0.3.

3.4. Cloning the Ovine B4GALNT2 cDNA Sequence

Based on reverse transcription cDNA from ovine granule cells , which were cultured in vitro, six fragments of B4GALNT2 conserved sequences were successfully amplified using P4–P9 (Figure 2a–f). A sequence length of 2653 bp of the sheep B4GALNT2 gene was assembled from the six partial conserved sequences. Then, 5′ and 3′UTR sequences were detected by the RACE method. Using two RACE primers (5′GP1–5′GP2), two transcription start sites (TSS) were discovered in 5′UTR (Figure 2g–h). Using the 3′RACE GSP inner primer (3′GIP) and 3′RACE GSP outer primer (3′GOP), a product of 924 bp based on B4GALNT2 3′UTR was cloned (Figure 2i). After sequencing and assembling the conserved sequences of 5′UTR and 3′UTR, a transcript of 3528 bp named B4GALNT2a and a transcript of 3514 bp named B4GALNT2b were submitted to NCBI. The accession number of B4GALNT2a (KY120333) and B4GALNT2b (KY120334) should be released on 16 November 2018.

3.5. Characterization of the Ovine B4GALNT2 cDNA Sequences

Genomic alignments indicated that the full-length cDNA sequence of B4GALNT2a and B4GALNT2b were all composed of 11 exons. Sequence analysis of B4GALNT2a and B4GALNT2b showed that they owned the same 3′UTR of 1924 bp and the same ORF of 1521 bp in size, which encoded for a 506 amino acid peptide. The difference between B4GALNT2a and B4GALNT2b was the length of 5′UTR; in other words, B4GALNT2 possessed two transcription start sites (TSS), one of which was located at 83 bp, and the other of which that was located at 69 bp to the ATG (initiation codon) on the left (Figure 2j).

3.6. Feature and Structure Prediction of the Ovine B4GALNT2 Protein

Hydrophobicity analysis of the ovine B4GALNT2 protein indicated that the maximum hydrophobicity value was 3.167 in the position of 20 aa, and the minimum was −2.689 in the position of 483 aa (Figure 3a). The maximum and minimum average flexibility index values of ovine B4GALNT were 20.503 for the 121 aa position and 0.372 for the 416 aa position; however, the value of 0.379 for the 24 aa position is also worth pointing out and is discussed further below (Figure 3b). Then, SMART was used to speculate the conservative domains. There were a transmembrane region sequence at 9–31 aa, low complexity sequence at 117–128 aa, and Glycosyl transferase family 2 sequence at 264–421 aa, respectively (Figure 3c). The mutation of g.36933082C > T caused the residue change of P/S in the position of 288 aa, which belonged to the Glycosyl transferse family 2 domain. Therefore, this mutation should be considered more important than the other three mutations found in this study.
Secondary structural prediction showed that ovine B4GALNT2 is comprised of 25.49% alpha helix, 24.90% beta sheet, and 49.61% random coil (Supplementary File 3). The tertiary structures of ovine B4GALNT2 were predicted by Phyre2. The results showed that the prediction model was based on a template of Nucleotide-diphospho-sugar transferases (d1xhba2), and only 243 residues (48% of the ovine B4GALNT2 sequence, 261–504 aa) have been modelled with 100.0% confidence by the single highest scoring template (Figure 3d).

3.7. Amino Acid Sequence Analysis of Ovine B4GALNT2

ProtParam was used to predict the physicochemical properties of amino acid sequences, and the molecular weight and isoelectric point of ovine B4GALNT2 were 57,443.4 Da and 8.86, respectively. The amino acid composition of the B4GALNT2 protein showed that the highest proportion of the B4GALNT2 protein was 12.1% for Leu, and the lowest was 1.0% for Trp.
The predictions of subcellular localization contribute to our understanding of the protein function and its physical and chemical environment in vivo [30]. Position 9–31 aa of the B4GALNT2 protein was predicted as being transmembrane helices (Figure 4a), and it was classified as a secretory pathway protein. Three disulphide bonds (cysteine pairs: 389–406, 453–504, and 79–81), two N-glycosylation sites (Asn232 and Asn305) and twenty-six phosphorylation sites (composed by ten Ser, eight Thr, and eight Tyr) were predicted in B4GALNT2 (Figure 4b,c).

3.8. Multiple Sequence Alignment and Phylogenetic Analysis

Six high similarity protein sequences (the ovine B4GALNT2 amino acid sequence was performed blastp in the NCBI based on the database of mammal’s Swiss-Prot for searching) were selected (Supplementary File 4), and searched for the three most important motifs based on MEME (Figure 4d). In the amino acid sequence of ovine B4GALNT2, segments of 294–343 aa, 404–453 aa, and 206–255 aa were the most important regions for the motifs. The nucleotide sequence of B4GALNT2 in some models and domesticated animals were chosen in order to construct phylogenetic trees for the gene identified as homologous to ovine B4GALNT2 (Supplementary File 5). Then, a molecular phylogenetic tree was constructed by the Neighbor-Joining method, with 1000 Bootstrap replications in MEGA software (Version 6.0). At first glance, Figure 4e shows that the orthologous genes of ovine B4GALNT2 in various species were clustered together first, paralogous genes were clustered later, and mammals were clustered versus Xenopus tropicalis.

3.9. B4GALNT2 Expression Profile in STH Sheep and Tan Sheep

To explore the differential expression patterns of B4GALNT2 between high and low fecundity sheep breeds, qRT-PCR was performed on the cDNA of 13 tissues in STH sheep and Tan sheep. As shown in Figure 5, B4GALNT2 was expressed in all of the detected tissues in the two sheep breeds. The B4GALNT2 expression quantities in the ovary, kidney and lung were significantly higher than in the other tissues in STH sheep (p < 0.05); however, only the ovarian B4GALNT2 expression quantity was significantly higher than that of other tissues in Tan sheep (p < 0.05). Comparing the expression in the same tissue between two sheep breeds, expression levels was significantly different in the kidney and oviduct (p < 0.05). As the fellow tissues of the HPG axis, the hypothalamus and pituitary were lower than other tissues in the expression of B4GALNT2.

4. Discussion

In France, the FecL mutation could be regarded as the best positional and expressional candidate for the high fecundity gene in Lacaune sheep breeds [17]. The female population of Lacaune sheep breeds is composed of 71% ++ ewes, 27% + L ewes, and 2% LL ewes. + L ewes produce 0.5 more lambs per lambing on average than ++ ewes [31]. In the present study, two mutations of g.36938224T > A and g.37034573A > G in intron of B4GALNT2 and one mutation of DLX3:c. * 803A > G linked with the FecL site have not been found, which means that the difference in reproduction among these selected sheep breeds have nothing to do with the FecL mutation. However, two mutations of g.36946470C > T and g.36933082C > T in the exon of B4GALNT2 had a significant effect on litter size in the first parity for STH Sheep (p < 0.05). Meanwhile, more data for the litter size of STH sheep should be collected to validate this conclusion.
Then, B4GALNT2 cDNA was successively cloned from ovine granule cells, which were cultured in vitro. 5′RACE and 3′RACE were used to explore the full-length cDNA for the first time, and two transcription start sites (TSS) were obtained in 5′UTR, which meant alternative splicing existed in the B4GALNT2 transcripts. Up to now, there has only been one transcript, which was included in NCBI. The transcription start sites (TSS) of 3514 bp fragments were the same as described in the research of Drouilhet et al. [17], which was in accordance with the transcript in NCBI. As early as 2003, human full-length clones of the B4GALNT2 gene were obtained from the human colon cancer cell line Caco-2 [21,32]. Multiple transcripts diverged in their 5′ and 3′UTR, and some of them were very long (about 9000 bp), and the first exons existed as two alternative splices at least [33]. In many other glycosyltransferase genes, such as β1,4-galactosyltransferase, β4GT-I, and α2,3-sialyltransferase ST3Gal IV, multiple transcripts existed as well [34,35,36]. The transcriptional direction of ovine B4GALNT2 was opposite to the established DNA sequence for mice, cattle, goats, pigs, and Rhesus monkeys, while the B4GALNT2 transcriptional direction in humans and dogs was the exception. The two splicing isoforms of ovine B4GALNT2 discovered in the present study were all contained in 11 exons, and had the same CDS of 1521 bp in size, which could encode a 506 amino acid peptide. To date, the verified human B4GALNT2 transcripts in NCBI declared three alternative splicing fragments existed, and each length of its CDS was different produced with different lengths of residue. Therefore, there may be other alternative splicing fragments of ovine B4GALNT2 gene, which remain to be found.
Based on the predicted data of subcellular localization, transmembrane helices, hydrophobicity, and average flexibility index of the B4GALNT2 protein, we suggest that the positions from 20 aa to 24 aa for the protein were possibly crucial for its normal function. The results of the transmembrane helices and conservative domains analysis showed that a transmembrane region existed in the position of 9–31 aa, and we can speculate that the ovine B4GALNT2 protein belonged to the pathway of secretory. According to the database of UniProt, the human B4GALNT2 protein was localized on the Golgi apparatus membrane [32,37]. Therefore, we can infer that the ovine B4GALNT2 protein may also be localized on the Golgi apparatus membrane. The B4GALNT2 protein in human transfers a beta-1,4-linked GalNAc to the galactose residue of an alpha-2,3-sialylated chain found on both N- and O-linked glycans [17,32]. In Lacaune sheep, DBA and KM694 staining were used to detect the different glycoprotein profiles, which were targeted by B4GALNT2 between L/L and +/+ ewes. Ten specific glycoproteins presented only in the follicular fluids of L/L ewes, including inhibin α and βA subunits, which lead to the production of Activin A and Inhibin A and finally influence the ovarian function [17].
Based on homology modeling, the tertiary structure prediction of the ovine B4GALNT2 protein only covered the position of 261–504 aa, and the result was consistent with the speculation of conservative domains, in which a Glycosyl transferse family 2 sequence was located in the position of 264–421 aa. The positions of 416 aa (the minimum average flexibility index), 483 aa (the minimum value of hydrophobicity), and 389 aa and 406 aa (a pair of disulphide bonds) were marked on the tertiary structure. 453 aa and 504 aa should have also made up a pair of disulphide bonds based on the SCRATCH protein predictor (http://scratch.proteomics.ics.uci.edu/); however, their positions were far away from each other in the predicted tertiary structure. As it turned out, the evidence suggests that tertiary structure prediction in the present study offered limited utility. After multiple sequence alignment of the amino acid sequence, six high similarity sequences analyzed with MEME revealed that the three most important motifs were located in the sequence of the Glycosyl transferse family 2, which verified the speculation of the conservative domain.
Although the two linked mutations (mutation g.36938224T > A and mutation g.37034573A > G) were not located in the exons of B4GALNT2, Drouilhet et al. took into account the discovery that the B4GALNT2 gene expressed in L/L granulosa and theca cells was exhibited at a 1000 fold higher rate than in +/+, and this finally supported the B4GALNT2 gene as the candidate gene for FecL [17]. The new viewpoint of the B4GALNT2 gene acting as the FecL gene was announced widely by researchers for the reason that this gene affects litter size in a different way, which have nothing to do with the TGFβ/BMP signal pathway [1,17,38,39]. The mutation of g. 36946470C > T caused the residue change of P/L in the positing of 160aa, the position of which has no important domain for the protein. However, the mutation of g.36933082C > T caused the residue change of P/S in the position of 288 aa, and the position belonged to the Glycosyl transferse family 2 domain (264–421 aa). Therefore, this mutation of g.36933082C > T should be considered more important than the mutation of g. 36946470C > T in this study.
In the present study, the expression quantities of B4GALNT2 in the ovary were all significantly higher than those of other tissues in STH sheep and Tan sheep, which was consistent with the results of Drouilhet et al. [17]. Except for the kidney and oviduct, no significant differences in expression level was found between the two breeds in the other tissues. The expression results suggest that the B4GALNT2 gene should play an important role in the ovine ovary, while having little correlation with differences between STH sheep and Tan sheep in reproduction. Li et al. reported that B4GALNT2 is expressed in the colon, kidney, intestine, oviduct, and ovary. B4GALNT2 is up-regulated by progesterone and down-regulated by estrogen in mice, and progesterone-induced up-regulation of B4GALNT2 might contribute to the implantation process [40,41]. The mice B4GALNT2 protein was detected in the whole cumulus-oocyte, and Lin had proven that the B4GALNT2 protein was essential for cumulus expansion, which was a critical step during oogenesis [42]. The B4GALNT2 protein was localized in the granulosa cells and the antral follicular fluid of Lacaune sheep (L/L) ovaries as well, and performed the transfers of beta-1,4-linked GalNAc to the galactose residue of an alpha-2,3-sialylated chain [32]. Mice with oocytes generating glycoproteins lacking core 1-derived O-glycans and complex N-glycans had been regarded as a new model of follicular premature ovarian failure [43]. These findings proved the vital importance of glycosylation in the control of ovarian function, and pointed to a new direction of discovery in the gene pathway of ovine reproduction.

5. Conclusions

In summary, the selected 11 sheep breeds had no variation in the three specific mutation sites, which are closely linked to FecL mutation. However, two mutations of g.36946470C > T and g.36933082C > T in the exon of B4GALNT2 had a significant effect on litter size in the first parity for STH Sheep (p < 0.05). Two transcription start sites (TSS) were discovered from 5′UTR of B4GALNT2 in ovine granule cells in vitro. B4GALNT2 is mainly expressed in the ovine ovary, suggesting that B4GALNT2 plays an important role in sheep reproduction. The pathway of B4GALNT2, which is different from the BMP pathway, is a new direction of research to further understand ovine ovarian function. Our findings and analysis of ovine B4GALNT2 will help us to further understand its expression and function, and also may contribute to exploring its role in the ewe reproduction system.

Supplementary Materials

The following are available online at https://www.mdpi.com/2076-2615/8/10/160/s1. Supplementary File 1: Sequences of the primers used in the amplifications. Supplementary File 2: Haplotype block in B4GALNT2. Supplementary File 3: Predicted secondary structures of the ovine B4GALNT2 protein. Supplementary File 4: Six high similarity protein sequences of ovine B4GALNT2 for motif detection. Supplementary File 5: Homologous mRNA sequences of ovine B4GALNT2 for phylogenetic tree construction.

Author Contributions

These studies were designed by X.G., X.W. and M.C., X.G., X.W., X.H. and B.L. performed all the experimental analyses and prepared all the figures and tables. X.G. and X.W. analyzed the data and drafted the manuscript. R.D., Q.L., W.H., J.Z., X.Z. and M.C. contributed to revisions of the manuscript. X.Z. and M.C. assisted in explaining the results and revised the final version of the manuscript.

Funding

This research was funded by National Natural Science Foundation of China (No. 31472078 and No. 31772580), Earmarked Fund for China Agriculture Research System (No. CARS-38), Central Public-interest Scientific Institution Basal Research Fund (No. Y2017JC24, No. 2018ywf-yb-2), Agricultural Science and Technology Innovation Program of China (No. ASTIP-IAS13), China Agricultural Scientific Research Outstanding Talents and Their Innovative Teams Program, China High-level Talents Special Support Plan Scientific and Technological Innovation Leading Talents Program (No. W02020274), Tianjin Agricultural Science and Technology Achievements Transformation and Popularization Program (No. 201704020). And the APC was funded by National Natural Science Foundation of China (No. 31472078).

Conflicts of Interest

All authors declare no conflicts of interest.

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Figure 1. Target amplification bands for three specific mutations. (a) Target band amplified by P1 for the mutation g.36938224T > A. (b) Target band amplified by P2 for the mutation g.37034573A > G. (c) Target band amplified by P3 for the mutation DLX3:c. * 803A > G. (d) The sequencing result at the site of g.36938224T > A. (e) The sequencing result at the site of g.37034573A > G. (f) The sequencing result at the site of DLX3:c. * 803A > G.
Figure 1. Target amplification bands for three specific mutations. (a) Target band amplified by P1 for the mutation g.36938224T > A. (b) Target band amplified by P2 for the mutation g.37034573A > G. (c) Target band amplified by P3 for the mutation DLX3:c. * 803A > G. (d) The sequencing result at the site of g.36938224T > A. (e) The sequencing result at the site of g.37034573A > G. (f) The sequencing result at the site of DLX3:c. * 803A > G.
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Figure 2. Full-length sequence of B4GALNT2. (a) Partial cording sequence amplified by P4. (b) Partial cording sequence amplified by P5. (c) Partial cording sequence amplified by P6. (d) Partial cording sequence amplified by P7. (e) Partial cording sequence amplified by P8. (f) Partial cording sequence amplified by P9. (g) 5′RACE product for the transcript of B4GALNT2a. (h) 5′RACE product for the transcript of B4GALNT2b. (i) 3′RACE product for the B4GALNT2 gene. (j) Gene structures of the B4GALNT2a and B4GALNT2b transcripts. RACE, rapid amplification of cDNA ends.
Figure 2. Full-length sequence of B4GALNT2. (a) Partial cording sequence amplified by P4. (b) Partial cording sequence amplified by P5. (c) Partial cording sequence amplified by P6. (d) Partial cording sequence amplified by P7. (e) Partial cording sequence amplified by P8. (f) Partial cording sequence amplified by P9. (g) 5′RACE product for the transcript of B4GALNT2a. (h) 5′RACE product for the transcript of B4GALNT2b. (i) 3′RACE product for the B4GALNT2 gene. (j) Gene structures of the B4GALNT2a and B4GALNT2b transcripts. RACE, rapid amplification of cDNA ends.
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Figure 3. Feature and structure prediction of the ovine B4GALNT2 protein. (a) Hydrophobicity analysis of the B4GALNT2 protein. (b) Average flexibility index of the B4GALNT2 protein. (c) Predicted conservative domains of the B4GALNT2 protein. (d) Prediction of partial sequence for B4GALNT2 in tertiary structures.
Figure 3. Feature and structure prediction of the ovine B4GALNT2 protein. (a) Hydrophobicity analysis of the B4GALNT2 protein. (b) Average flexibility index of the B4GALNT2 protein. (c) Predicted conservative domains of the B4GALNT2 protein. (d) Prediction of partial sequence for B4GALNT2 in tertiary structures.
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Figure 4. Amino acid sequence analysis of ovine B4GALNT2 and its multiple sequence alignments. (a) Predicted transmembrane helices of the B4GALNT2 protein. (b) Predicted N-glycosylation sites of the B4GALNT2 protein. (c) Predicted phosphorylation sites of the B4GALNT2 protein. (d) Prediction of the three most important motifs in the B4GALNT2 protein. (e) Phylogenetic tree based on the homology nucleotide sequence for B4GALNT2.
Figure 4. Amino acid sequence analysis of ovine B4GALNT2 and its multiple sequence alignments. (a) Predicted transmembrane helices of the B4GALNT2 protein. (b) Predicted N-glycosylation sites of the B4GALNT2 protein. (c) Predicted phosphorylation sites of the B4GALNT2 protein. (d) Prediction of the three most important motifs in the B4GALNT2 protein. (e) Phylogenetic tree based on the homology nucleotide sequence for B4GALNT2.
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Figure 5. B4GALNT2 expression profile in STH sheep and Tan sheep. Note: Lowercase letters indicate significant differences among tissues in Small Tail Han sheep, and capital letters indicate differences among tissues in Tan sheep. Means with the same letter were not significantly different (p < 0.05). The symbol of “*” indicates significant differences (p < 0.05) between STH sheep and Tan sheep in same tissues.
Figure 5. B4GALNT2 expression profile in STH sheep and Tan sheep. Note: Lowercase letters indicate significant differences among tissues in Small Tail Han sheep, and capital letters indicate differences among tissues in Tan sheep. Means with the same letter were not significantly different (p < 0.05). The symbol of “*” indicates significant differences (p < 0.05) between STH sheep and Tan sheep in same tissues.
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Table
Table 1. SNPs for missense in the ovine B4GALNT2 gene.
Table 1. SNPs for missense in the ovine B4GALNT2 gene.
ChromosomePositionCodonsResidues ChangeResidues PositionSourceVariant ID
chr11g.36971115CAC/TACH/Y68missensers595977899
g.36946470CCA/CTAP/L160missensers426776354
g.36946465GCT/ACTA/T162missenseNA
g.36942215ATT/ACTI/T197missensers423653795
g.36933082CCA/TCAP/S288missensers405227267
g.36933070GTG/ATGV/M292missensers426513123
g.36930089CAT/CAGH/Q433missensers402747554
Note: NA indicates Not Applicable to its column.
Table
Table 2. Allele and genotype frequencies of B4GALNT2 in Small Tail Han (STH) ewes.
Table 2. Allele and genotype frequencies of B4GALNT2 in Small Tail Han (STH) ewes.
Polymorphic Site
(CDS Position)		GenotypeGenotype Frequency (N)AlleleAllele Frequencyχ2 (p)
g.36971115C > T (C205T)CC0.85 (74)C0.920.40 (0.53)
CT0.14 (12)T0.08
TT0.11 (1)
g.36946470C > T (C482T)CC0.68 (59)C0.820.78(0.38)
CT0.27 (23)T0.18
TT0.05 (4)
g.36933082C > T (C865T)CC0.81 (71)C0.91.01 (0.32)
CT0.19 (17)T0.1
TT0 (0)
g.36930089T > G (T1302G)TT0.69 (61)T0.820.87 (0.35)
TG0.26 (23)G0.18
GG0.05 (4)
Note: p > 0.05 indicates the locus was under Hardy-Weinberg equilibrium.
Table
Table 3. Litter size and standard error of STH ewes in different parities for each genotypes.
Table 3. Litter size and standard error of STH ewes in different parities for each genotypes.
Polymorphic SiteGenotypeLitter Size (Means ± S.E.)
First Parity (N)Second Parity (N)Third Parity (N)Total (N)
g.36971115C > TCC2.18 ± 0.1 (68)2.37 ± 0.13 (52)2.7 ± 0.22 (23)2.43 ± 0.08 (144)
CT2.36 ± 0.2 (11)2.43 ± 0.37 (7)3 ± 0 (3)2.60 ± 0.23 (21)
TT1 ± 0 (1)2 ± 0 (1)2.00 ± 0 (1)1.67 ± 0.52 (3)
g.36946470C > TCC2.17 ± 0.11 (54) b2.32 ± 0.16 (38)2.87 ± 0.27 (15)2.45 ± 0.10 (107) b
CT2.32 ± 0.18 (22) b2.37 ± 0.19 (19)2.6 ± 0.26 (10)2.43 ± 0.13 (51) b
TT1.25 ± 0.25 (4) a2.33 ± 0.333(3)2.00 ± 1 (2)1.58 ± 0.38 (7) a
g.36933082C > TCC2.08 ± 0.09 (64) a2.32 ± 0.14 (47)2.57 ± 0.2 (21)2.32 ± 0.09 (132) b
CT2.59 ± 0.24 (17) b2.5 ± 0.25 (14)3.29 ± 0.42 (7)2.79 ± 0.15 (38) a
TTNANANANA
g.36930089T > GTT2.11 ± 0.12 (55)2.32 ± 0.15 (41)2.8 ± 0.25 (20)2.41 ± 0.09 (116)
TG2.43 ± 0.15 (23)2.5 ± 0.2 (18)2.5 ± 0.22 (6)2.48 ± 0.15 (47)
GG1.67 ± 0.33 (3)2 ± 0 (2)3.00 ± 1 (2)2.22 ± 0.35 (7)
Note: Values with the same superscript for the same column have no significant difference (p > 0.05). Values with a different superscript for the same column have significant differences (p < 0.05).

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MDPI and ACS Style

Guo, X.; Wang, X.; Liang, B.; Di, R.; Liu, Q.; Hu, W.; He, X.; Zhang, J.; Zhang, X.; Chu, M. Molecular Cloning of the B4GALNT2 Gene and Its Single Nucleotide Polymorphisms Association with Litter Size in Small Tail Han Sheep. Animals 2018, 8, 160. https://doi.org/10.3390/ani8100160

AMA Style

Guo X, Wang X, Liang B, Di R, Liu Q, Hu W, He X, Zhang J, Zhang X, Chu M. Molecular Cloning of the B4GALNT2 Gene and Its Single Nucleotide Polymorphisms Association with Litter Size in Small Tail Han Sheep. Animals. 2018; 8(10):160. https://doi.org/10.3390/ani8100160

Chicago/Turabian Style

Guo, Xiaofei, Xiangyu Wang, Benmeng Liang, Ran Di, Qiuyue Liu, Wenping Hu, Xiaoyun He, Jinlong Zhang, Xiaosheng Zhang, and Mingxing Chu. 2018. "Molecular Cloning of the B4GALNT2 Gene and Its Single Nucleotide Polymorphisms Association with Litter Size in Small Tail Han Sheep" Animals 8, no. 10: 160. https://doi.org/10.3390/ani8100160

APA Style

Guo, X., Wang, X., Liang, B., Di, R., Liu, Q., Hu, W., He, X., Zhang, J., Zhang, X., & Chu, M. (2018). Molecular Cloning of the B4GALNT2 Gene and Its Single Nucleotide Polymorphisms Association with Litter Size in Small Tail Han Sheep. Animals, 8(10), 160. https://doi.org/10.3390/ani8100160

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