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Article

Genome-Wide Identification and Transcriptional Expression of the METTL21C Gene Family in Chicken

by
Ge Yang
†,
Hongzhao Lu
†,
Ling Wang
,
Jiarong Zhao
,
Wenxian Zeng
and
Tao Zhang
*
School of Biological Science and Engineering, Shaanxi University of Technology, Hanzhong, Shaanxi 723001, China
*
Author to whom correspondence should be addressed.
†
These authors contributed equally to this work.
Genes 2019, 10(8), 628; https://doi.org/10.3390/genes10080628
Submission received: 26 June 2019 / Revised: 6 August 2019 / Accepted: 15 August 2019 / Published: 20 August 2019
(This article belongs to the Section Animal Genetics and Genomics)
Browse Figures
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Abstract

:
The chicken is a common type of poultry that is economically important both for its medicinal and nutritional values. Previous studies have found that free-range chickens have more skeletal muscle mass. The methyltransferase-like 21C gene (METTL21C) plays an important role in muscle development; however, there have been few reports on the role of METTL21C in chickens. In this study, we performed a genome-wide identification of chicken METTL21C genes and analyzed their phylogeny, transcriptional expression profile, and real-time quantitative polymerase chain reaction (qPCR). We identified 10 GgMETTL21C genes from chickens, 11 from mice, and 32 from humans, and these genes were divided into six groups, which showed a large amount of variation among these three species. A total of 15 motifs were detected in METTL21C genes, and the intron phase of the gene structure showed that the METTL21C gene family was conservative in evolution. Further, both the transcript data and qPCR showed that a single gene’s (GgMETTL21C3) expression level increased with the muscle development of chickens, indicating that the METTL21C genes are involved in the development of chicken muscles. Our results provide some reference value for the subsequent study of the function of METTL21C.

1. Introduction

The chicken (Gallus gallus domesticus) may originate from red junglefowl (G. gallus) [1]. Lueyang black-bone chicken is a famous native chicken breed with some distinctive features, such as its low fat content, strong muscles, and considerable nutritional and medicinal values. It has been listed in the Poultry Genetic Resources of China and was identified as a National Geographical Indication Product [2]. Chicken feeding methods are generally divided into caged and free range. It has been found that free-range chickens have more muscle mass [3]. A previous study showed that METTL21C is a skeletal-muscle-specific lysine methyltransferase [4]. It is well known that skeletal muscle plays an important role in the development of chickens, and can affect the athletic ability of the chickens. Thus, it is relevant to explore the role of the METTL21C gene in the muscle development of chicken species.
The methyltransferase-like 21C gene (METTL21C) belongs to the METTL21 family of the methyltransferase superfamily; in humans, METTL21C is located on 13q33.1 and is also called C13orf39 [5]. METTL21C, which has protein-lysine N-methyltransferase activity and participates in protein modification [6], is one of the protein methyltransferases (MTases) and exists in most eukaryotic organisms. It catalyzes the transfer of a methyl group from the cofactor S-adenosylmethionine (AdoMet) to a substrate and mainly occurs on lysine and arginine. MTases catalyze different biological reactions in organisms, which regulate many different substrates, such as lipids, RNA, DNA, small molecules, and proteins [7,8,9]. METTL21C, which performs regular protein structure housekeeping such as folding and proofreading, is also a 70 kDa heat shock protein which acts as an ATP-dependent (Adenosine triphosphate dependent) molecular chaperone [10]. Further, bivariate genome-wide association studies (GWAS) have found that METTL21C can also act as a pleiotropic factor on muscles [11]. METTL21C can regulate calcium homeostasis in bones and muscles and promote the differentiation of myoblasts to myotubes through the nuclear factor (NF)-kB signaling pathway [11]. In addition, METTL21C may also reduce apoptotic osteocytes and regulate intracellular homeostasis [12]. A previous study concluded that METTL21C is an important regulator of protein degradation in skeletal muscles under normal and enhanced proteolytic conditions [4]. This suggests that METTL21C is closely related to the development of muscles and thus deserves further exploration.
The paralog of METTL21C is METTL21D, which is also a protein methyltransferase. Widely found in eukaryotes, METTL21D can catalyze the trimethylation of Lys315 in valosin-containing protein (VCP) in vitro, so it is also called VCP-KMT (valosin containing protein lysine methyltransferase) [6]. VCP is found in all eukaryotes and is a highly conserved AAA+ protein (ATPase associated with various cellular activities) [13]. It is a homotyped hexamer cyclic molecule comprising four domains: a flexible N-terminal domain and a short C-terminal domain, which may bind to the substrate, and two AAA ATP-binding domains [14,15,16]. VCP participates in a wide range of biological activities, including homotypic membrane fusion [17], endoplasmic reticulum-related degradation [18], DNA repair [19], and mitochondrial autophagy [20]. VCP and hereditary inclusion body myopathy are associated with Paget disease and frontotemporal dementia (inclusion body myopathy with early-onset Paget disease and frontotemporal dementia (IBMPFD)), which primarily affects muscles and the brain [21]. The pathogenesis of IBMPFD is due to the autosomal dominant single amino acid replacing the VCP terminal domain and the highly conserved residues within the D1 domain [21,22]. As mentioned above, VCP includes four domains; the domain D1 is one of the two AAA ATP-binding domains and so the mutation of the VCP gene is involved in the pathogenesis of IBMPFD [21]. In a recent study, it was found that METTL21D could promote tumor metastasis and affect cell growth, migration, and infection [23]. Since METTL21C is a homologous sequence of METTL21D, it was found that METTL21C interacts with VCP and catalyzes the modification and trimethylation of lysine 315 [4]. The METTL21C gene family from G. gallus domesticus offers an exceptional opportunity to study the evolution and function of muscle development systems [24]. In this study, to detect the mechanism of METTL21C in the development of chicken muscles, according the global genomic data on chickens, mice, and humans published by others, we systematically characterized 10 METTL21C genes of G. gallus, 11 METTL21C genes of Mus musculus, and 32 METTL21C genes of Homo sapiens. We used an iterative process of manual and computational analyses to identify examples of METTL21C in G. gallus, M. musculus, and H. sapiens encoding a gene family within the latest-released G. gallus, M. musculus, and H. sapiens whole-genome sequences [25,26,27]. We constructed a phylogenetic tree of the METTL21C gene family, the conserved motifs, gene structure, protein domain, and chromosome localization and further analyzed G. gallus METTL21C genes. To understand the function of the METTL21C genes in G. gallus, we also studied the transcriptional-level expression profiles of METTL21C of different tissues at different developmental stages. Our results provide useful theoretical support for the functional characterization of these METTL21C genes that are involved in the age-development process of G. gallus.

2. Materials and Methods

2.1. Identification of METTL21C in Sequenced Genomes of G. gallus

The query sequences of the METTL21C genes downloaded from the National Center for Biotechnology (NCBI) database (http://asia.ensembl.org/info/data/ftp/index.html) were for G. gallus, M. musculus, and H. sapiens. The whole protein sequence of G. gallus (http://asia.ensembl.org/info/data/ftp/index.html?tdsourcetag=s_pcqq_aiomsg) was also downloaded from the NCBI database (http://asia.ensembl.org/info/data/ftp/index.html). Based on these sequences, using the BLASTP (basic local alignment search tool) software with E-value parameters less than 1e-10, a total of 22 genes were examined as the candidate sequence. To further check the members of the METTL21C gene family, we used a profile hidden Markov model (HMM) implemented with default parameters in HMMER v3.2.1 for Windows (http://hmmer.org/download.html/) according to the domain named pfam10007 [28].

2.2. METTL21C Protein Alignment, Phylogenetic Analysis, Pfam Domain Detection, and Chromosome Location Analysis of G. gallus METTL21C Genes

MEGA software was used to do a complete alignment based on the checked sequence with default settings [29], and an unrooted phylogenetic tree was constructed based on alignments using the neighbor-joining (NJ) method with pairwise deletion of 1000 bootstraps and a Poisson model. According to this phylogenetic analysis result, we classified these genes into different groups [30,31], and the conserved domains of these 119 METTL21C protein sequences were detected in Batch software (https://www.ncbi.nlm.nih.gov/Structure/bwrpsb/bwrpsb.cgi). Those domains found by Pfam were also detected by the SMART program (http://smart.embl-heidelberg.de/) with an E-value cutoff of 1.0 to validate the final result. Based on the GFF (general feature format) file, we anchored these genes to the related genomes through the MapChart software (http://mapchart.software.informer.com/2.2/) using the default parameters. The GFF file of these three species was downloaded from the NCBI database (https://www.ncbi.nlm.nih.gov/genome/?term=).

2.3. Gene Structure and Motif Analysis of METTL21C Genes

The exon–intron structure was illustrated using the online gene structure display server program (http://gsds.cbi.pku.edu.cn/) according to the information in the GFF file of the METTL21C gene family. The motifs were identified using the multiple EM (emphasize) for motif elicitation (MEME) program using the default parameters [32]. The parameters were as follows: the maximum number of motifs was set to 20, and the optimum motif width was set to 30–50.

2.4. The Materials, Treatments, and Collections of Different Breeds of Chickens

A total of six different breeds of black-bone chickens were collected, they included 20-day-old Liangfenghua chickens, 20-day-old Qingjiaoma chickens, 60- and 120-day-old Siyu chickens, and 60- and 120-day-old Lueyang black-bone chickens. For each chicken development time, we considered periods of 20, 60, and 120 days. We raised these chickens in cages or free-range: Lueyang black-bone chickens were free-range and the rest were caged. Different breeds of chickens had different feeding conditions. All the chickens are under normal circumstances, the optimal temperature for each stage of silky fowl through the brooding period (0~6 weeks) is as follows: 0~3 days is 38~36 °C, with a decrease of 2~3 °C every week to 6 weeks. The temperature should be gradually reduced by 21~18 °C; the optimum temperature for broiler chickens after 6 weeks of age is 21~16 °C. The humidity in the house should be controlled by a hygrometer. The optimum suitable humidity for chicks is 55%~65%, and that of adult chickens is 60%~70%. Regarding the illumination, chicks of 1 to 3 days old maintain 23 to 24 h of light, 4 to 14 days of age maintain 16 to 19 h of light, and after 15 days of age, 8 to 9 h of light are maintained, and artificial light is applied when sunshine is insufficient. Free-range care generally does not require artificial control of the growing environment, and if necessary, some measures are taken according to the weather.

2.5. Materials, Treatments, and Collection of the Transcriptome Profile of the METTL21C Gene Gamily of Chickens

We put the samples in liquid nitrogen prior to storage at −80 °C until use [33]. Total RNA was isolated using an RNA-prep Pure Kit (Tiangen, China) [34,35]. Libraries for RNA sequencing (RNA-seq) were produced using NEBNext Ultra RNA Library Prep Kit (NEB, Beverly, MA, USA). Paired-end sequencing was performed on the Illumina HiSeq2500 platform to generate 100 bp reads using default parameters (Novogene Bioinformatics Technology Co., Ltd., Beijing, China (www.novogene.cn)). The de novo transcriptome was assembled using default settings in Trinity [36] and was based on the well-genome reference of chickens [37]. The assembled RNA-seq data were used to quantify these gene expression levels based on their fragments per kilobase of exon per million reads mapped (FPKM) values using Cufflinks with default parameters [38]. For each member’s expression level of the METTL21C gene family, we used the HemI 1.0 software with default parameters [32,39]. For the expression level of several METT21C genes with error bars, the ggplot2 R package was used [40].

2.6. Quantitative Real-Time PCR

Because METTL21C is related to muscle development, we collected the skeletal muscle of different breeds at the same anatomic sites, such as the soleus muscle for the Siyu, Lueyang, Liangfenghua, and Qingjiaoma chickens. We also collected stomach, gizzard, lung, skeletal muscle, liver, skin, and myocardium from the Lueyang chickens (Table S1, Supplementary Materials). Total RNA was extracted from individual chicken tissues (stomach, gizzard, lung, skeletal muscle, liver, skin, and myocardium) and reverse transcribed to produce first-strand cDNA as described above. Real-time amplification reactions were performed on a 7500 fast real-time PCR system (Applied Biosystems, USA). The relative expression level of each gene was calculated according to the 2−ΔΔCt method [41]. The β-actin gene was used as an internal control [42], and all analyses were performed with three technical and three biological replicates (Table S2, Supplementary Materials).

3. Results

3.1. Identification and Phylogenetic Analysis of METTL21C Genes

To identify METTL21C-encoding genes, we seeded files for the lysine methyltransferase domains from G. gallus, M. musculus, and H. sapiens. We acquired 119 candidate METTL21C genes from these three species, including 22 G. gallus genes, 31 M. musculus genes, and 66 H. sapiens genes. To check for the presence of the lysine methyltransferase domain, those 119 candidate protein sequences were reduced to 53 genes that contain the same conserved domain as the lysine methyltransferase. Finally, we found 53 METTL21C genes in all species. In order to explore the evolutionary relationship among the members of the METTL21C families, an NJ tree based on G. gallus, M. musculus, and H. sapiens protein sequences was constructed (Figure 1). These three species had 10, 11, and 32 METTL21C genes, respectively. Based on the completed alignment of the sequences and the phylogenetic analysis, we divided a total of 53 members of chickens, mice, and humans into six groups, named groups I to VI. (Table S3, Supplementary Materials). We found that group I contained 8 METTL21Cs, group II contained 10 METTL21Cs, group III contained 6 METTL21Cs, group IV contained 6 METTL21Cs, group V contained 5 METTL21Cs, and group VI contained 18 METTL21Cs. We found four G. gallus METTL21Cs (GgMETTL21C7, GgMETTL21C8, GgMETTL21C4, and GgMETTL21C3) to be closely associated with M. musculus, and six G. gallus METTL21Cs (GgMETTL21C9, GgMETTL21C5, GgMETTL21C1, GgMETTL21C2, GgMETTL21C6, and GgMETTL21C10) were found to be closely associated with H. sapiens.

3.2. Chromosomal Locations of METTL21C Genes and Their Relationship with G. gallus

The 10 METTL21C genes were distributed unevenly in the G. gallus chromosomes based on the physical positions. We found the distribution of the METTL21C genes were different on each of the six chromosomes (Table 1; Figure 2). The accession number of the coding sequence and the genomic and protein IDs are listed in Table 1. Chromosomes 8 and 18 contained only one gene, GgMETTL21C1 and GgMETTL21C6, respectively, whereas GgMETTL21C3 and GgMETTL21C4 were both found on chromosome 1, but in different positions. GgMETTL21C2 and GgMETTL21C5, GgMETTL21C7 and GgMETTL21C8, as well as METTL21C9 and GgMETTL21C10 were found at different positions chromosomes chr14, chr7, and chr5, respectively (Figure 2).

3.3. METTL21C Gene Structures and Conserved Motifs

To better understand the relationship between the structure and functions among METTL21C genes of G. gallus, M. musculus, and H. sapiens, the exon/intron organization and conserved motifs were analyzed and are shown in Figure 3. To compare the structural components of the 53 METTL21C genes, their structures, including exons and introns, were mapped. The maximum number of exons was found in MmMETTL21C9 (nine exons), and the minimum number of one exon was found in GgMETTL21C6. It seems that the most closely related members had similar numbers of exons. For example, those in Group I mostly had one exon, such as GgMETTL21C6, HsMETTL21C1, HsMETTL21C2, MmMETTL21C3, and MmMETTL21C4, but HsMETTL21C23 had six exons and GgMETTL21C10 had five exons. Members in Group II mostly had three exons, Group III mostly had nine exons, Group IV mostly had three exons, Group V had a varying number of exons (three to five), and Group VI mostly had three exons. Interestingly, we found there were one to nine exons in G. gallus, for example, GgMETTL21C6 had one exon, while GgMETTL21C5 had nine exons.
We also found using the MEME program that the METTL21C genes have 15 motifs. Motif 1 was mostly present in all breeds except GgMETTL21C7, HsMETTL21C7, HsMETTL21C14, HsMETTL21C22, and GgMETTL21C10. Motif 2 appeared in G. gallus, except GgMETTL21C9. As expected, the most closely related members in the same subfamilies shared a common motif composition, which may be indicative of similar function. These results suggest that all METTL21C genes in G. gallus share at least one typical domain.

3.4. Expression Profile Analysis of G. gallus METTL21C Genes

To understand the expression patterns of different genes in the METTL21C gene family, we tested the expression levels of 10 genes in six samples from four breeds of chickens based on RNA-seq data (Table S4, Supplementary Materials). Based on phylogenetic analysis and expression levels, we divided the 10 members of chickens into three groups, named groups A, B, and C (Figure 4). Meanwhile, based on the different expression levels, we noticed that the expression levels of GgMETTL21C4, GgMETTL21C6, GgMETTL21C5, and GgMETTL21C10 were lowest and there was no difference in the different breeds and different development periods. Our results showed that GgMETTL21C7 and GgMETTL21C8 had relatively high expression in G. gallus, and there were some differences among the different samples. The expression patterns of GgMETTL21C7 and GgMETTL21C8 have breed specificity. Interestingly, we also detected that GgMETTL21C7, GgMETTL21C8, and GgMETTL21C2 genes had lower expression of Ly120 compared with Ly60. However, we found that GgMETTL21C3 had a large difference between chickens of different varieties. GgMETTL21C3 was highly expressed in Lueyang chickens and had a higher expression of Ly120 compared with Ly60.

3.5. Real-Time PCR of METTL21C Genes of the METTL21C Gene Family

These different breeds of chickens were not significantly different for growth in morphology, based on quantitative real-time PCR analysis of the expression of METTL21C3 in Sy and Ly chickens. The results showed that METTL21C3 was highly expressed in 120 days of Ly chickens (Figure 4 and Figure 5a). Using β-actin as the internal reference gene, qPCR was used to detect the expression level of METTL21C3 in seven chicken tissues of Ly chickens, and it was found that the expression levels of myocardial and skeletal muscles were higher (Figure 5c). Based on quantitative real-time PCR analysis of the expression of METTL21C3 in soleus muscles and toe elongation muscles of Qjm and Ly chicken, we found that the expression level of METTL21C3 increased significantly with age (Figure 5d,e). Finally, we found that the expression level of METTL21C3 in free-range chickens was higher by comparing the expression levels of METTL21C3 in caged chickens and free-range chickens, further indicating that the METTL21C3 gene is indeed associated with muscle growth and development.

4. Discussion

4.1. The Characteristics of the METTL21C Gene Family

METTL21C is a skeletal-muscle-specific lysine methyltransferase which plays a critical role in the development of bones and muscles [4]. The METTL21C gene family is closely related to osteoporosis and sarcopenia by the NF-kB signaling pathway to prevent the differentiation of myoblasts [11]. The METTL21C genes of chickens contained three conserved domains identified in NCBI-Batch-CDD (NCBI Batch conserved domain database), including the AdoMet_MTases superfamily, SAM_superfamily, and FAM86, suggesting that METTL21Cs are extremely conservative in evolution (Figure S1). We found all chicken METTL21C genes had the conserved domain of AdoMet_MTases. The key domain is AdoMet_MTases (Figure S1), and in general, the most common methyl donor is S-adenosyl-L-methionine (AdoMet). The methylation reactions often occur in cells, which are catalyzed by MTases and induce methyl transfer from donor substrate molecules, implying that these genes have a similar function (Figure S1) [43]. In chickens, the number of domains of AdoMet_MTases is larger than that of other domains, such as the domain of SAM and FAM86.
The gene family is structurally and functionally similar and contains a common domain. For the METTL21C gene, the lysine methyltransferase domain was determined in a total of 10 member groupings in the METTL21C gene family. Based on phylogenetic analysis, the METTL21Cs are divided into six subfamilies named Groups I to VI. The present study identified 10 METTL21C genes in chickens, and more in M. musculus and H. sapiens (Table 1). The proteomes of these animals are different. For example, the M. musculus proteome is about 46,930 kb, and the H. sapiens proteome is about 70,940 kb. However, the G. gallus proteome is about 25,209 kb. Comparative analysis suggested that chickens, mice, and humans have similar numbers of gene families [26,27,44], indicating that the number of METTL21Cs in different species is not determined by the genome size (Table 1).
In previous studies, GgMETTLC1 was called METTL23, which is a GABPA (GA-binding protein transcription factor, α subunit) function regulator that plays an important role in the transcriptional regulation of human cognition [45,46] and affects the nervous system and brain development [47]. Thus, we speculated that GgMETTL21C1 could be related to brain development in chickens. In terms of GgMETTL21C2, it contains the FAM86A protein that belongs to the protein MTases family, which catalyzes the trimethylation of eukaryotic elongation factor 2 (eEF2) on Lys-525 [48], indicating that the GgMETTL21C2 is involved in protein synthesis, which is critical for cell survival during stress [49]. In this study, GgMETTL21C3 was highly expressed in Lueyang chickens, compared to other breeds (Figure 4 and Figure 5), and highly expressed in skeletal muscles compared to other muscles (Figure 5e). With the development of muscles in chickens, the expression level of GgMETTL21C3 is increased, these results show that GgMETTL21C3 is related to the development of skeletal muscles of Lueyang breeds (Figure 4 and Figure 5a–d). In a previous study, Philippe referred to GgMETTL21C5 as METTL22, which can mediate methylation of kin17 on lysine 135. The kin17 is a DNA/RNA-binding protein that participates in the replication and repair of DNA and the process of pre-mRNA [50], and we found that GgMETTL21C5 plays an important role in chickens. In a previous study, Magnus found that METTL21A acts as a protein MTase, which is involved in the trimethylation of a conserved lysiner [51], this study also named the unnamed ID, which will enable others to identify the gene more clearly (Table S5, Supplementary Materials).

4.2. The Evolution History of the METTL21C Gene Family of Chickens, Humans, and Mice

Gene structure is an important factor for gene family evolution [52]. The location of the gene coding sequence and the structure of the protein are largely determined by the position of the intron, and protein diversity is further increased by exon shuffling and alternative splicing [53,54]. The association of the intron phase with conservation at splice site sequences is related to the evolution of spliceosomal introns. Intron phase 0 indicates the highest conservation, intron phase 1 also shows high conservation, and intron phase 2 shows the lowest conservation [55,56]. In the case of the METTL21C genes in chickens, almost all of the genes’ structure was intron phase 0, so the METTL21C genes were conservative in evolution (Figure 3c). In conclusion, based on these analyses, including motif and gene structure, we showed that METTL21C genes were conservative in evolution. We found that the METTL21C gene structure of chickens is different from that of humans and mice. The structure of METTL21Cs in chickens has undergone evolutionary changes (Figure 2c).
Conserved motif analysis revealed that almost all the METTL21C proteins contained one to five subdomains (Figure S1, Supplementary Materials). In addition, each subfamily had other special motifs, while some subfamilies also harbored specific motifs (Figure 3c). Interestingly, we found that the METTL21C genes of the same subfamily have a similar gene structure. This indicated that the gene structures are relatively conserved within each subfamily. For each subfamily, gene structures of METTL21C genes from chickens, mice, and humans are almost identical, suggesting that exon–intron structures of METTL21C genes are relatively conserved between these species. In particular, the GgMETTL21C10 gene has a long genetic distance, a simple genetic structure, and only one domain, probably because of the lack of structure during the evolution process (Figure 3). Its domain may be the AdoMet_MTases superfamily. Motif 1 existed in almost the entire METTL21C gene family of these three species, which means that the METTL21C gene family is conservative in evolution (Figure 3a).

4.3. The Function of the METTL21C Gene Family of Chickens

To detect the expression level of the METTL21C gene family members in different breeds of chickens, we sequenced six RNA-seq from different species at different periods. We then examined the expression level of METTL21C genes in different species of chickens (Table S1, Supplementary Materials). Based on the phylogenetic analysis and METTL21Cs’ expression level, we divided these 10 genes into three groups. Group A included GgMETTL21C3, GgMETTL21C4, GgMETTL21C9, GgMETTL21C7, and GgMETTL21C8. Group B included GgMETTL21C1, GgMETTL21C2, and GgMETTL21C6. Group C included GgMETTL21C5 and GgMETTL21C10 (Figure 1). In previous studies, the METTL21C genes showed different expression patterns during different periods (20, 60, and 120 days) in Lfh, Qjm, Sy, and Ly (Table S1, Supplementary Materials). However, there have been few reports on the METTL21C gene family in chickens. As the number of days increased, we found that the expression of METTL21C also increased, implying that these genes of METTL21C play a critical role in the development of chickens (Figure 4). The results showed that the METTL21C gene family can catalyze the development of bone and muscle [8]. Interestingly, GgMETTL21C7 and GgMETTL21C8 are in the same subfamily (Figure 1) and their expression was almost the same, indicating that these two genes are related to the growth and development of chickens [4]. Group C had a low expression level (Figure 4). The expression level of METTL21C3 increased with the growth and development of chickens, further indicating that this gene may inhibit apoptosis and promote bone and muscle development (Figure 4) [4]. Importantly, the transcript data showed that, compared with Ly60, GgMETTL21C3 was highly expressed in Ly120, implying that GgMETTL21C3 plays an important role in the development of Lueyang species. Otherwise, by comparing the relative expression levels of METTL21C in Sy and Ly at 60 days and 120 days, it was found that GgMETTL21C was highly expressed in Ly at 120 days (Figure 5a); this evidence showed that GgMETTL21C3 is involved in the development of chickens. Therefore, we detected the relative expression of GgMETTL21C3 in different tissues of Ly chickens and found that the expression level was higher in skeletal muscle and myocardium (Figure 5b), further verifying that GgMETTL21C is related to skeletal muscle [4]. We also found that METTL21C is related to the growth and development of muscles in different breeds of chickens (Figure 5a,b) and in different feeding methods (Figure 5e). Both the transcript and qPCR analyses showed that GgMETTL21C3 is involved in the muscle development of Lueyang black-bone chickens, which is consistent with previous studies [4,11,12].

5. Conclusions

In this study, we identified 10 METT21C genes in G. gallus. Phylogenetic analysis showed that the METTL21C genes can be divided into six groups based on specific and special domains. The 10 GgMETTL21Cs were respectively distributed on seven different chromosomes, with some colocalized to the same chromosome, such as GgMETTL21C7 and GgMETTL21C8 located in chromosome 7. Motif 1 was found in humans, mice, and chickens; Motifs 1, 5, 2, and 6 were found in most human HsMETTL21C genes; Motifs 1, 2, 5, and 8 were found in most mouse MuMETTL21C genes; and Motifs 1, 2, and 8 were found in most chicken GgMETTL21C genes. Based on this, we speculate that the conserved sequences are present in the METTL21C family. Expression profile analysis revealed that METTL21C gene family members display diverse expression patterns at different ages of different chickens. A total of three genes (GgMETTL21C3 GgMETTL21C7, and GgMETTL21C8) had high expression levels in G. gallus, suggesting they might play an important role in the development of chickens. In particular, the transcript data and qPCR analysis both showed that a single gene called METTL21C3 is involved in the development of different muscles of the Lueyang species, such as the soleus, long extensor digitorum, myocardium, and leg muscles. This study provides strong evidence that METTL21C3 may play a critical role in the development of chicken muscles.

Supplementary Materials

The following are available online at https://www.mdpi.com/2073-4425/10/8/628/s1, Figure S1: Conserved domain of the METTL21C family identified in 10 chickens (G. gallus). Table S1: A total of six samples of chicken muscles used for expression profiling in this study. Table S2: Primer information of qPCR. Table S3: The distribution numbers of METTL21C genes in Groups I–VI. Table S4: Expression data of METTL21C genes in flowers at different developmental stages of chickens (G. gallus). Table S5: Previous names of the METTL21C gene.

Author Contributions

Conceptualization, G.Y.; Data curation, H.L., L.W. and J.Z.; Funding acquisition, H.L. and T.Z.; Software, L.W. and W.Z.; Writing—original draft, G.Y., H.L. and T.Z.; Writing—review and editing, G.Y., H.L. and T.Z.

Funding

This study was supported by the Shaanxi Province Agricultural Science and Technology Innovation Project (2019NY-097) and the National Natural Science Foundation of China (NSFC) (31402071).

Acknowledgments

We thank Feng Yan, Ruiqing Li, and Jiarong Zhao for the sample collection.

Conflicts of Interest

The authors declare no conflict of interests.

References

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Figure 1. Phylogenetic analysis of methyltransferase-like 21C (METTL21C) proteins in G. gallus domesticus, M. musculus, and H. sapiens. These 53 sequences were used to construct a neighbor-joining (NJ) tree. The tree was divided into six groups (I–VI); the names of the different groups are displayed.
Figure 1. Phylogenetic analysis of methyltransferase-like 21C (METTL21C) proteins in G. gallus domesticus, M. musculus, and H. sapiens. These 53 sequences were used to construct a neighbor-joining (NJ) tree. The tree was divided into six groups (I–VI); the names of the different groups are displayed.
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Figure 2. Chromosomal location in chickens of METTL21C genes on six chromosomes. Chromosomal locations in G. gallus are at the top of each bar. The scale of the chromosome is millions of base pairs (Mb).
Figure 2. Chromosomal location in chickens of METTL21C genes on six chromosomes. Chromosomal locations in G. gallus are at the top of each bar. The scale of the chromosome is millions of base pairs (Mb).
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Figure 3. (a) Phylogenetic relationships, (b) motif compositions, and (c) gene structures of the 53 METTL21C genes identified in G. gallus (Gg), M. musculus (Mm), and H. sapiens (Hs). (a) Phylogenetic relationships using the NJ method, and different colors represent different groups. (b) Colored boxes indicate conserved motifs, and gray lines represent nonconserved sequences. The length of motifs in each protein is shown proportionally. (c) UTR represents upstream, CDS represents coding sequence, and EXON represents exon.
Figure 3. (a) Phylogenetic relationships, (b) motif compositions, and (c) gene structures of the 53 METTL21C genes identified in G. gallus (Gg), M. musculus (Mm), and H. sapiens (Hs). (a) Phylogenetic relationships using the NJ method, and different colors represent different groups. (b) Colored boxes indicate conserved motifs, and gray lines represent nonconserved sequences. The length of motifs in each protein is shown proportionally. (c) UTR represents upstream, CDS represents coding sequence, and EXON represents exon.
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Figure 4. Expression patterns in METTL21C of G. gallus. The heat map was drawn in log10-transformed expression values. Red and blue represent relatively high and low expression, respectively, compared to the control. Lfh represents the chicken of Liangfenghua; Qjm represents the chicken of Qingjiaoma; Sy represents the chicken of Siyu; Ly represents the chicken of Lueyang. The numbers represent the age of the chickens in days.
Figure 4. Expression patterns in METTL21C of G. gallus. The heat map was drawn in log10-transformed expression values. Red and blue represent relatively high and low expression, respectively, compared to the control. Lfh represents the chicken of Liangfenghua; Qjm represents the chicken of Qingjiaoma; Sy represents the chicken of Siyu; Ly represents the chicken of Lueyang. The numbers represent the age of the chickens in days.
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Figure 5. Relative mRNA expression: (a) METTL21C relative mRNA expression expression in different breeds of Sy and Ly chicken. (b) METTL21C relative mRNA expression in different tissues of Ly chicken. (c) METTL21C mRNA expression level in the soleus muscle. Lueyang represents Lueyang chickens and Qingjiao represents Qingjiao chickens. (d) METTL21C mRNA expression level in toe elongation muscles. (e) METTL21C relative mRNA expression in caged and free-ranging chickens.* p ≤ 0.05; ** p ≤ 0.01.
Figure 5. Relative mRNA expression: (a) METTL21C relative mRNA expression expression in different breeds of Sy and Ly chicken. (b) METTL21C relative mRNA expression in different tissues of Ly chicken. (c) METTL21C mRNA expression level in the soleus muscle. Lueyang represents Lueyang chickens and Qingjiao represents Qingjiao chickens. (d) METTL21C mRNA expression level in toe elongation muscles. (e) METTL21C relative mRNA expression in caged and free-ranging chickens.* p ≤ 0.05; ** p ≤ 0.01.
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Table
Table 1. Methyltransferase-like 21C (METTL21C) gene family information in chickens (G. gallus).
Table 1. Methyltransferase-like 21C (METTL21C) gene family information in chickens (G. gallus).
Gene NameProtein IDCDS IDGene IDChromosomeGene Position
StartEnd
GgMETTL21C1ENSGALP00000002756.3ENSGALT00000002759.6ENSGALG00000001790.6chr184,245,5904,247,698
GgMETTL21C2ENSGALP00000003173.1ENSGALT00000003178.2ENSGALG00000002044.5chr1413,793,04113,797,471
GgMETTL21C3ENSGALP00000027192.5ENSGALT00000027243.7ENSGALG00000016864.7chr1144,281,168144,285,163
GgMETTL21C4ENSGALP00000027185.6ENSGALT00000027236.7ENSGALG00000016859.7chr1144,171,934144,190,015
GgMETTL21C5ENSGALP00000053406.2ENSGALT00000048292.2ENSGALG00000033603.3chr1410,511,22210,519,988
GgMETTL21C6ENSGALP00000047914.1ENSGALT00000056245.2ENSGALG00000035963.2chr85,470,2265,471,907
GgMETTL21C7ENSGALP00000063245.1ENSGALT00000086206.2ENSGALG00000008493.7chr712,179,29612,182,133
GgMETTL21C8ENSGALP00000032767.3ENSGALT00000033408.5ENSGALG00000008493.7chr712,179,72512,182,133
GgMETTL21C9ENSGALP00000020014.7ENSGALT00000020041.7ENSGALG00000012269.7chr557,863,10657,866,374
GgMETTL21C10ENSGALP00000073336.1ENSGALT00000098371.1ENSGALG00000051460.1chr557,862,38757,869,575
Note: Protein ID, gene ID, CDS ID, and gene position indicate that the accession numbers of the METTL21C gene family member sequences were downloaded from the National Center for Biotechnology (NCBI). CDS: Coding sequence.

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Yang, G.; Lu, H.; Wang, L.; Zhao, J.; Zeng, W.; Zhang, T. Genome-Wide Identification and Transcriptional Expression of the METTL21C Gene Family in Chicken. Genes 2019, 10, 628. https://doi.org/10.3390/genes10080628

AMA Style

Yang G, Lu H, Wang L, Zhao J, Zeng W, Zhang T. Genome-Wide Identification and Transcriptional Expression of the METTL21C Gene Family in Chicken. Genes. 2019; 10(8):628. https://doi.org/10.3390/genes10080628

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Yang, Ge, Hongzhao Lu, Ling Wang, Jiarong Zhao, Wenxian Zeng, and Tao Zhang. 2019. "Genome-Wide Identification and Transcriptional Expression of the METTL21C Gene Family in Chicken" Genes 10, no. 8: 628. https://doi.org/10.3390/genes10080628

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