Analysis of Dip2B Expression in Adult Mouse Tissues Using the LacZ Reporter Gene

Disconnected (disco)-interacting protein 2 homolog B (Dip2B) is a member of the Dip2 superfamily and plays an essential role in axonal outgrowth during embryogenesis. In adults, Dip2B is highly expressed in different brain regions, as shown by in situ analysis, and may have a role in axon guidance. However, the expression and biological role of Dip2B in other somatic tissues remain unknown. To better visualize Dip2B expression and to provide insight into the roles of Dip2B during postnatal development, we used a Dip2btm1a(wtsi)komp knock-in mouse model, in which a LacZ-Neo fusion protein is expressed under Dip2b promoter and allowed Dip2B expression to be analyzed by X-gal staining. qPCR analyses showed that Dip2b mRNA was expressed in a variety of somatic tissues, including lung and kidney, in addition to brain. LacZ staining indicated that Dip2B is broadly expressed in neuronal, reproductive, and vascular tissues as well as in the kidneys, heart, liver, and lungs. Moreover, neurons and epithelial cells showed rich staining. The broad and intense patterns of Dip2B expression in adult mice provide evidence of the distribution of Dip2B in multiple locations and, thereby, its implication in numerous physiological roles.

The Dip2 gene was first identified and studied in Drosophila.Dip2 is a novel transcription factor that binds Disconnected protein (Disco) and supports proper neuronal connection during larva visual system development [4][5][6].Drosophila Dip2 is expressed in brain lobes and the ventral cord during embryogenesis and regulates axonal bifurcation of mushroom body neurons through the regulation of c-Jun N-terminal kinase [7,8].In Caenorhabditis elegans, Dip2 is expressed in most neurons, including VNC motor neurons, HSN, PVD, and mechanosensory neurons, as well as in epidermal cells.It is known that Dip2 functions in maintaining neuronal morphology and axon regrowth after injury [9].
In humans, Northern blot analysis revealed that DIP2B is expressed in the brain, placenta, skeletal muscle, heart, kidneys, pancreas, lungs, spleen, and colon and may be associated with neurocognitive problems linked with the fragile site FRA12a on chromosome 12q13.1 [3].Several bioinformatics studies have also discovered associations between DIP2B and numerous diseases, including schizophrenia, coronary artery disease (CAD), cervical squamous cell carcinoma, and colorectal cancer [10][11][12][13].In mice, mDip2 mRNA remains specific to the developing nervous system and may provide positional cues required for axon pathfinding and patterning [1].According to the International Knockout Mice Consortium (IKMC) program, Dip2b knockout decreases circulating free fatty acid and leukocyte numbers [14,15].Although a previous report produced evidence for the expression of the Dip2 gene in mice using Northern blot analysis, until now, validated tools and protocols for in situ Dip2b expression analysis in mice using the LacZ (β-galactosidase) reporter have not been available.In addition, in vivo analysis of Dip2b gene expression in non-neuronal cell types remains unknown.Notably, the physiopathological roles of DIP2B in mammals are still far from clear.
Recently, we reported that Dip2B is widely expressed during embryogenesis and its loss leads to prenatal lethality, possibly due to abnormal lung development [16].In the present study, we aimed to delineate, in detail, the tissues that may require Dip2B in adults by characterizing and analyzing the expression of Dip2B using Dip2b tm1a(wtsi)komp (Dip2b Tm1a ) knock-in mice generated by the Knockout Mouse Project (KOMP) [17].Transgenic expression of LacZ can be easily detected by enzyme histochemical staining using chromogenic substrates such as 5-bromo-4-chloro-3-indolyl-β-D-galactosidase (X-gal), 5bromo-indolyl-β-O-galactopyranoside (Bluo-gal), and derivatives thereof.β-Galactosidase hydrolyzes X-gal to form a highly sensitive blue precipitate [18][19][20][21][22][23][24].Subsequently, reporter gene approaches involved the detection of LacZ, another enzyme, or fluorescent proteins, have been used in many studies to characterize gene expression patterns in animals.The LacZ reporter is particularly useful since it requires no special imaging equipment and requires only standard histochemical staining methods.The whole-mount and frozen sections of Dip2b Tm1a knock-in mice were stained with X-gal, in parallel with wild-type littermate controls.

Animals
Dip2b tm1a (KOMP)wtsi (Dip2b tm1a/+ ) mice were purchased from the Knockout Mice Project (KOMP), while C57BL/6J mice were purchased from Vital River (Beijing, China).All mice were kept in a clean facility in Northeast Normal University.All animals were kept in IVC cages with free access to water and food at 20 • C and 50 ± 20% relative humidity under a 12/12 h light/dark cycle and pathogen-free conditions.All experimental procedures were conducted based on the Guide for Care and Use of Laboratory Animals of National Institutes of Health and approved by the Institutional Animal Care and Use Committee of Northeast Normal University (NENU/IACUC, AP2013011).The mice were sacrificed using 1% pentobarbital anesthesia at a dose of 10 mg/kg.Three biological replicates for Dip2b tm1a/+ and wild-type littermates of the same age were used in every experiment.

Genotyping
Genomic DNA from the adult mice was extracted from their tail tips and genotyped by PCR as previously described.Briefly, a tail sample was digested in GNTK-Proteinase K solution at 55-60 • C overnight and lysate boiled for 15 min, centrifuged at 1200 rpm, and subjected to PCR using the following conditions: 94 • C for 2 min; followed by 30 cycles of denaturation at 94 • C for 30 s, annealing at 60 • C for 30 s, and extension at 72 • C for 30 s; and final extension at 72 • C for 5 min, then held at 4 • C. PCR products were electrophoresed on 0.8% agarose gels.The nucleotide sequences of the PCR primers for genotyping were as follows: tm1a-F-TGAGACTGAGCTTGGCTACCACA and tm1a-R-TCCTCC TACATAGTTGGCAGTGT, and wt-F-AGTTAAGGCTGAGCATGGTGGGA and wt-R-TAGGGCTCTCACAGATCAGAGCT.
For frozen section X-gal staining, the tissues were incubated in 20% sucrose overnight at 4 • C and then embedded in an OCT compound (Tissue-Tek, Torrance, CA, USA) and frozen at −80 • C. Serial cryosections of 18 µm thickness were cut and collected onto Superfrost TM plus microscope slides.Sections were then dried on a slide warmer, fixed with 2% PFA for 10 min, and washed in rinsing buffer.X-gal staining was performed in a dark chamber at 37 • C overnight or until the desired staining was observed.After staining, the sections were fixed in 4% PFA for 5 min and washed in PBS.The sections were counter-stained in 0.25% eosin solution.Whole-mount and frozen section images were taken using an Olympus microscope (SXL-ILLB2-200, Tokyo, Japan) and a Canon digital camera (DSI26431, Tokyo, Japan).

Genotyping of Dip2b tm1a Mice
LacZ reporter mice have made a huge contribution to revealing gene expression patterns in vivo and in vitro.Dip2b is one of the genes that has never been systematically studied, neither in terms of expression nor function, although many critical biological roles have been suggested.Studying Dip2b expressing results on a knockout first, reportertagged insertion strategy involving Dip2b tm1a mice to generate a conditional and null allele.The targeted Dip2b tm1a (komp) wtsi allele carries a targeted trap "tm1a" knockout-first allele, promoterless selection cassette inserted into the seventh intron of the Dip2b gene consisting of an internal ribosome entry site (En2) that allows internal translation to start from ATG of the LacZ gene, splice acceptor (sA) site that provides trans-splicing of the LacZ-Neo cassette onto exon 7, and a fusion cDNA of LacZ and Neo (Figure 1A).The presence of the splice acceptor results in expression of a truncated Dip2b transcript leading to production of Dip2B containing only the first 311 of 2971 amino acids.Tm1a locus genotyping was performed using primers tm1a-F and tm1a-R to give a mutant specific band of 300 bp.The wild-type primers wt-F and wt-R amplify the intron 7 region and provide a product of 350 bp (Figure 1B).

021, 1, 3
the LacZ-Neo cassette onto exon 7, and a fusion cDNA of LacZ and Neo (Figure 1A).The presence of the splice acceptor results in expression of a truncated Dip2b transcript leading to production of Dip2B containing only the first 311 of 2971 amino acids.Tm1a locus genotyping was performed using primers tm1a-F and tm1a-R to give a mutant specific band of 300 bp.The wild-type primers wt-F and wt-R amplify the intron 7 region and provide a product of 350 bp (Figure 1B).

Expression of LacZ in the Nervous System
To address the activity of the regulatory region of Dip2b in the nervous system, whole-mount and frozen sections of the brain, spinal cord, and retina of 8-week-old heterozygous male Dip2b tm1a/+ and wild-type (WT) mice were subjected to LacZ staining.Whole-mount staining of ventral and dorsal brain orientation demonstrated strong signals widely spread among the two olfactory lobes (OLs), cerebral hemisphere (CH), superior and inferior colliculus (coli; colr), pons (PON), and cerebellum (CB) (Supplementary Figure S1A,B).Control littermates were negative for any X-gal signals (Supplementary Figure S1C,D).However, a detailed expression pattern was clearly understood only after performing frozen section staining of the brain (Supplementary Figure S1E,F).LacZ staining of 25 μm frozen section revealed strong signals in the cortex-dense ii/iii layers, scattered evenly in the iv layer (Figure 2A), hippocampal Ammon's horn (CA1, CA2, and CA3) including the dentate gyrus (Figure 2B), Purkinje cell layer and granular layer of the cerebellum (Figure 2C), ventral striatum (Figure 2D), olfactory nucleus (Figure 2E), and olfactory bulb consisting of the inner plexiform and outer glomerular layers (Figure 2F).Whole-mount staining allowed the detection of LacZ signals throughout the spinal cord in Dip2b tm1a/+ (Figure 2G).A 25 μm cross-section of the Dip2b tm1a/+ spinal cord revealed en-

Expression of LacZ in the Nervous System
To address the activity of the regulatory region of Dip2b in the nervous system, wholemount and frozen sections of the brain, spinal cord, and retina of 8-week-old heterozygous male Dip2b tm1a/+ and wild-type (WT) mice were subjected to LacZ staining.Whole-mount staining of ventral and dorsal brain orientation demonstrated strong signals widely spread among the two olfactory lobes (OLs), cerebral hemisphere (CH), superior and inferior colliculus (coli; colr), pons (PON), and cerebellum (CB) (Supplementary Figure S1A,B).Control littermates were negative for any X-gal signals (Supplementary Figure S1C,D).However, a detailed expression pattern was clearly understood only after performing frozen section staining of the brain (Supplementary Figure S1E,F).LacZ staining of 25 µm frozen section revealed strong signals in the cortex-dense ii/iii layers, scattered evenly in the iv layer (Figure 2A), hippocampal Ammon's horn (CA1, CA2, and CA3) including the dentate gyrus (Figure 2B), Purkinje cell layer and granular layer of the cerebellum (Figure 2C), ventral striatum (Figure 2D), olfactory nucleus (Figure 2E), and olfactory bulb consisting of the inner plexiform and outer glomerular layers (Figure 2F).Whole-mount staining allowed the detection of LacZ signals throughout the spinal cord in Dip2b tm1a/+ (Figure 2G).A 25 µm cross-section of the Dip2b tm1a/+ spinal cord revealed endogenous β-galactosidase activity on gray matter and the central canal (Figure 2H).Wild-type litter-mates did not show any LacZ signals when whole-mount (Figure 2I) or frozen sections (Figure 2J) were stained under the same conditions.

LacZ Expression in the Reproductive System
Male and female reproductive organs were investigated, and LacZ expression was identified in the testes, epididymis, prostate gland, penis, vagina, ovaries, and oviduct (Figure 3).LacZ staining of the Dip2b tm1a/+ male reproductive system revealed strong expression in the testes and prostate gland, while non-specific expression was observed in the epididymis and seminal vesicle (Figure 3A-F).Upon sectioning of the testes, staining was detected around the cuboidal epithelium (CuEp) lining of convoluted seminiferous tubules, which house spermatocytes, spermatids, and Sertoli and Leydig cells (Figure 3G).In the epididymis-stained section, a signal was detected at columnar epithelium (CoEp) lining of ducts (Figure 3I).In the penis section, staining was visible in the epithelium of In the whole-mounted and frozen section LacZ staining of 8-week-old Dip2b tm1a/+ eyes, LacZ was strongly expressed in the optic nerve (Figure 2K,L), the outer stratified squamous epithelial layer of the cornea, and the retina.At high magnification, an X-gal signal was clearly visible in the retinal optic nerve fiber layer, outer nuclear layer, and external limiting membrane (Figure 2M).As expected, the control littermates (WT) did not show staining (Figure 2N-P).In summary, Dip2B expression as indicated by β-galactosidase activity was dominant in nervous system-oriented tissues comprising of the brain, spinal cord, and eye.

LacZ Expression in the Reproductive System
Male and female reproductive organs were investigated, and LacZ expression was identified in the testes, epididymis, prostate gland, penis, vagina, ovaries, and oviduct (Figure 3).LacZ staining of the Dip2b tm1a/+ male reproductive system revealed strong expression in the testes and prostate gland, while non-specific expression was observed in the epididymis and seminal vesicle (Figure 3A-F).Upon sectioning of the testes, staining was detected around the cuboidal epithelium (CuEp) lining of convoluted seminiferous tubules, which house spermatocytes, spermatids, and Sertoli and Leydig cells (Figure 3G).In the epididymis-stained section, a signal was detected at columnar epithelium (CoEp) lining of ducts (Figure 3I).In the penis section, staining was visible in the epithelium of glans and prepuce (PrEp and EpGi) (Figure 3K).In the prostate gland, staining was detected around the duct wall and acne (Figure 3M).Wild-type littermates did not show any X-gal signals upon sectioning (Figure 3H,J,L,N).
Curr.Issues Mol.Biol.2021, 1,5 glans and prepuce (PrEp and EpGi) (Figure 3K).In the prostate gland, staining was detected around the duct wall and acne (Figure 3M).Wild-type littermates did not show any X-gal signals upon sectioning (Figure 3H,J,L,N).In the Dip2b tm1a/+ female reproductive system, LacZ was strongly expressed in the ovaries, oviduct, and vagina (Figure 4).In the ovary section, a LacZ signal was detected in the oocyte cytoplasm embedded in the ovarian follicle (Figure 4A,B).In the oviduct section, staining was deposited on the columnar epithelium of the mucosal fold (Figure 4C).However, it is not clear whether the signal was restricted to epithelium only or spread along with peg cells and lamina propria.In the vagina section, staining was visible in the lining of the stratified squamous epithelium (SqEp) (Figure 4D).The wild-type tissue section did not show LacZ expression (Figure 4E-H).(G-N) Frozen section of a LacZ-stained male testis, epididymis, penis, and prostate gland.CuEp, cuboidal epithelium; CoEp, columnar epithelium; PrEp, perpetual epithelium; EpGi, glans epithelium.
In the Dip2b tm1a/+ female reproductive system, LacZ was strongly expressed in the ovaries, oviduct, and vagina (Figure 4).In the ovary section, a LacZ signal was detected in the oocyte cytoplasm embedded in the ovarian follicle (Figure 4A,B).In the oviduct section, staining was deposited on the columnar epithelium of the mucosal fold (Figure 4C).However, it is not clear whether the signal was restricted to epithelium only or spread along with peg cells and lamina propria.In the vagina section, staining was visible in the lining of the stratified squamous epithelium (SqEp) (Figure 4D).The wild-type tissue section did not show LacZ expression (Figure 4E-H).

LacZ Expression in the Digestive System
After performing whole-mount and frozen tissue sectioning of the esophagus, small intestine, large intestine, and stomach, LacZ-positive signals were detected in the squamous epithelium lining of the forestomach (Figure 5A-C), in the thick mucosa layer of the esophagus comprising the non-keratinized stratified squamous epithelium (SqEp) (Figure 5G,H), in the crypts of Lieberkühn and intestinal glands in the mucosal layer of the small intestine (Figure 5K), and on the epithelial surface of the tongue (Figure 5L).Wild-type samples counterstained with LacZ were devoid of any staining (Figure 5D-F,I,J).

LacZ Expression in the Digestive System
After performing whole-mount and frozen tissue sectioning of the esophagus, small intestine, large intestine, and stomach, LacZ-positive signals were detected in the squamous epithelium lining of the forestomach (Figure 5A-C), in the thick mucosa layer of the esophagus comprising the non-keratinized stratified squamous epithelium (SqEp) (Figure 5G,H), in the crypts of Lieberkühn and intestinal glands in the mucosal layer of the small intestine (Figure 5K), and on the epithelial surface of the tongue (Figure 5L).Wild-type samples counterstained with LacZ were devoid of any staining (Figure 5D-F,I,J).

LacZ Expression of in the Respiratory System
Staining of Dip2b tm1a/+ respiratory system comprising the lungs, trachea, and larynx were positive for β-galactosidase.In the lungs, whole-mount and frozen tissue sections showed strong and broad X-gal signals in the ciliated columnar epithelium (CoEp) lining of the bronchioles (Figure 6A,B).In the trachea, LacZ expression was strictly contained in its ciliated columnar epithelium (respiratory epithelium) (Figure 6C).Similarly, in the larynx cross-section, expression was detected in the distal stratified non-keratinizing squamous epithelium of the vocal folds (Figure 6D).were positive for β-galactosidase.In the lungs, whole-mount and frozen tissue sections showed strong and broad X-gal signals in the ciliated columnar epithelium (CoEp) lining of the bronchioles (Figure 6A,B).In the trachea, LacZ expression was strictly contained in its ciliated columnar epithelium (respiratory epithelium) (Figure 6C).Similarly, in the larynx cross-section, expression was detected in the distal stratified non-keratinizing squamous epithelium of the vocal folds (Figure 6D).

LacZ Expression in the Genitourinary System
X-gal staining on the genitourinary system of 8-week-old Dip2b tm1a/+ mice revealed strong signals in the kidneys and urinary bladder.Whole-mount and frozen tissue sections of the kidneys showed broad staining in the renal pelvis and sparse staining in the glomeruli (Figure 7A-C).In the urinary bladder, a non-specific signal was detected during the whole mount (data not shown), but after sectioning, specific staining was found in the transitional epithelium (Figure 7D).The adrenal glands showed X-gal signals strictly in the medulla, but not in the cortex (Figure 7E).

LacZ Expression in the Genitourinary System
X-gal staining on the genitourinary system of 8-week-old Dip2b tm1a/+ mice revealed strong signals in the kidneys and urinary bladder.Whole-mount and frozen tissue sections of the kidneys showed broad staining in the renal pelvis and sparse staining in the glomeruli (Figure 7A-C).In the urinary bladder, a non-specific signal was detected during the whole mount (data not shown), but after sectioning, specific staining was found in the transitional epithelium (Figure 7D).The adrenal glands showed X-gal signals strictly in the medulla, but not in the cortex (Figure 7E).

LacZ Expression in the Cardiovascular System
LacZ is strongly expressed in the circulatory system.Figure 8A-D shows wholemount staining of the vascular network collected from different parts of Dip2b tm1a/+ adult mice, including the tail, tongue, skin, and esophagus veins.Whole-mount and frozen tissue sections of the heart revealed LacZ signals in the atrium and the tunica media layer of ventricles (myocardium).However, it is not clear whether the signal is restricted to cardiac muscle fibers or endomysial connective tissue that contain capillaries (Figure 8E-G).

LacZ Expression in the Cardiovascular System
LacZ is strongly expressed in the circulatory system.Figure 8A-D shows whole-mount staining of the vascular network collected from different parts of Dip2b tm1a/+ adult mice, including the tail, tongue, skin, and esophagus veins.Whole-mount and frozen tissue sections of the heart revealed LacZ signals in the atrium and the tunica media layer of ventricles (myocardium).However, it is not clear whether the signal is restricted to cardiac muscle fibers or endomysial connective tissue that contain capillaries (Figure 8E-G).

LacZ Expression in the Cardiovascular System
LacZ is strongly expressed in the circulatory system.Figure 8A-D shows wholemount staining of the vascular network collected from different parts of Dip2b tm1a/+ adult mice, including the tail, tongue, skin, and esophagus veins.Whole-mount and frozen tissue sections of the heart revealed LacZ signals in the atrium and the tunica media layer of ventricles (myocardium).However, it is not clear whether the signal is restricted to cardiac muscle fibers or endomysial connective tissue that contain capillaries (Figure 8E-G).

Discussion
In this study, Dip2b expression in adult tissues was investigated using Dip2b-LacZ reporter mice.The results showed that the Dip2b gene is widely expressed in the tissues comprising neuronal and non-neuronal cell types.The expression of Dip2b in various tissues was validated by real-time quantitative PCR (qPCR) and the results showed high correlation with those from LacZ staining of the corresponding tissues (Figure 9).Hence, the results of LacZ expression faithfully reflect endogenous Dip2b expression (Table 1).

Discussion
In this study, Dip2b expression in adult tissues was investigated using Dip2b-LacZ reporter mice.The results showed that the Dip2b gene is widely expressed in the tissues comprising neuronal and non-neuronal cell types.The expression of Dip2b in various tissues was validated by real-time quantitative PCR (qPCR) and the results showed high correlation with those from LacZ staining of the corresponding tissues (Figure 9).Hence, the results of LacZ expression faithfully reflect endogenous Dip2b expression (Table 1).Although the functional role of the DIP2 protein in the nervous system has been characterized in Drosophila, its role in the nervous systems of mammals remains to be characterized.In this study, we found that Dip2b to be highly expressed in the nervous system.In the brain, Dip2b expression was detected in the neuronal cells of all brain regions, including forebrain neurons (granular cell layer of the olfactory bulb, the cerebral cortex, and the dentate gyrus), the hindbrain (granule and Purkinje cells of the cerebellum), pyramidal neurons of the hippocampus, the thalamus, cerebellar nuclei, and the pons region.In spinal cord, Dip2b expression was detected in gray matter mostly comprising efferent neurons, projection neurons, and interneurons and in the central canal.These expression results indicate that Dip2b may play a role in neurogenesis.This is supported, in part, by our recent studies on Dip2b expression and its potential role during neurite outgrowth in Dip2b tm1a/tm1a hippocampal cultured cell [25].A previous report suggested that Dip2b may play a role in mental retardation and in schizophrenia [3,12].In addition, this finding also supports a previous report of Dip2B signaling in axon guidance and synaptic transmission [1].Dip2B was initially identified as a binding partner of Disco in Drosophila by yeast two-hybrid screening.Mutation at this locus can cause abnormal neuronal connections in the visual system [6].This phenotype was well supported in our study, in which high LacZ expression was observed in retinal neurons.Our study showed that Dip2B is expressed in the vascular system, including the veins, arteries, and cardiomyocytes.Upon whole-mount staining, we observed LacZ expression in various veins, including the tongue, tail, and skin veins.This observation suggests the potential role of the Dip2b gene in vasculature.Integrative functional analysis of super-enhancer SNPs has shown Dip2b to be a novel functional locus for coronary artery disease [11].The strong and universal LacZ expression in cardiomyocytes may suggest a potential role of Dip2B in heart function.
Besides the nervous and cardiovascular systems, our studies demonstrated that Dip2B is expressed in other somatic tissues, including the reproductive, respiratory, genitourinary, and digestive systems.Strong expression of Dip2B was detected in the epithelial cells within the testes, epididymis, penis, urinary bladder, oviduct, vagina, bronchioles, trachea, tongue, esophagus, and forestomach, which suggests the possible role of Dip2B in epithelial cells.It has been reported that Dip2B may function as an epigenetic regulator responsible for the expansion of epithelial KIT + progenitor during organogenesis [26].In addition, bioinformatics analysis has implicated Dip2b as a target gene in the metastasis of cervical squamous cell carcinoma [13].LacZ expression was also detected in the prostate gland, oocytes, kidneys, adrenal glands, and intestinal glands.Cytological investigations are ongoing to identify the cell type-specific distribution of Dip2b gene expression and to elucidate possible functions of the Dip2b gene in these organs [16,25].

Conclusions
We investigated endogenous Dip2b gene expression in a Dip2 tm1a mouse model containing the LacZ reporter gene.We found that Dip2B is expressed in a variety of somatic tissues, including the brain, eyes, spinal cord, testes, epididymis, penis, prostate gland, vagina, ovaries, oviduct, heart, lungs, and kidneys.The results of this expression study will facilitate identification of the functional role(s) of Dip2B during postnatal development and in adults.In addition, the Dip2b tm1a reporter mouse line used here will be an excellent tool for future characterization of the cell lineage and fate of Dip2b-expressing cells during early embryonic development, as well as for future identification of the factors and functions regulated by Dip2B and its associated diseases.

Institutional Review Board Statement:
The study was conducted according to the guidelines of the Institutional Animal Care and Use Committee, and approved by the Ethics Committee of Northeast Normal University (protocol code AP2018011 and 1 January 2018).

Figure 1 .
Figure 1.Tm1a knockout-first reporter tagged insertion allele and genotyping.(A) Structure of Dip2b tm1a (KOMP) Wtsi allele .A critical exon is flanked by loxP sites, with FRT, lacZ, neo, and FRT elements upstream of the critical exon.(B) Genotyping PCR results for tail biopsy from Dip2b tm1a/+ intercrossing mice.A 300 bp band appeared on the gel for the transgene allele and a 350 bp band for the wildtype allele.

Figure 1 .
Figure 1.Tm1a knockout-first reporter tagged insertion allele and genotyping.(A) Structure of Dip2b tm1a (KOMP) Wtsi allele .A critical exon is flanked by loxP sites, with FRT, lacZ, neo, and FRT elements upstream of the critical exon.(B) Genotyping PCR results for tail biopsy from Dip2b tm1a/+ intercrossing mice.A 300 bp band appeared on the gel for the transgene allele and a 350 bp band for the wild-type allele.

Figure 2 .
Figure 2. LacZ expression in the nervous system.(A-F) Frozen section expression analysis of Dip2b tm1a/+ brain regions at high magnification.(A) LacZ protein expression is notable in cortex neurons, (B) the hippocampus and dentate gyrus, (C) the granular and Purkinje cell layer of the cerebellum, (D) the ventral striatum, (E) the olfactory nucleus, and (F) the inner plexiform and outer nucleus layer of the olfactory bulb in Dip2b tm1a/+ .(G-J) LacZ staining of the adult spinal cord.(G) Whole-mount staining of the adult spinal cord.(H) Longitudinal section of the spinal cord depicting LacZ signals in the gray matter and central canal in Dip2b tm1a/+ .(I,J) The wild-type whole-mounted and frozen sections were LacZ-negative.(K-P) LacZ staining in the adult eye.(K) Whole-mount staining of P56 mouse eyes, along with nerve fibers, showed LacZ staining.(L) Sagittal section of the eye stained for LacZ expression.The retinal wall and cornea showed LacZ expression in Dip2b tm1a/+ .(M) LacZ-positive retina of Dip2b tm1a/+ at high magnification showed strong signals in the external limiting membrane, outer nuclear layer, and optic nerve fiber layer.(N-P) Wild-type control was devoid of a LacZ-positive signal.

Figure 2 .
Figure 2. LacZ expression in the nervous system.(A-F) Frozen section expression analysis of Dip2b tm1a/+ brain regions at high magnification.(A) LacZ protein expression is notable in cortex neurons, (B) the hippocampus and dentate gyrus, (C) the granular and Purkinje cell layer of the cerebellum, (D) the ventral striatum, (E) the olfactory nucleus, and (F) the inner plexiform and outer nucleus layer of the olfactory bulb in Dip2b tm1a/+ .(G-J) LacZ staining of the adult spinal cord.(G) Whole-mount staining of the adult spinal cord.(H) Longitudinal section of the spinal cord depicting LacZ signals in the gray matter and central canal in Dip2b tm1a/+ .(I,J) The wild-type whole-mounted and frozen sections were LacZ-negative.(K-P) LacZ staining in the adult eye.(K) Whole-mount staining of P56 mouse eyes, along with nerve fibers, showed LacZ staining.(L) Sagittal section of the eye stained for LacZ expression.The retinal wall and cornea showed LacZ expression in Dip2b tm1a/+ .(M) LacZ-positive retina of Dip2b tm1a/+ at high magnification showed strong signals in the external limiting membrane, outer nuclear layer, and optic nerve fiber layer.(N-P) Wild-type control was devoid of a LacZ-positive signal.

Figure 4 .
Figure 4. LacZ expression in the female reproductive system.(A) Cross-section of the ovary of a non-pregnant mouse.LacZ expression is visible in the ovarian follicles and oviduct.(B,C) High magnification of ovarian follicles and oviduct.(D) Section of the vagina with a LacZ signal at the stratified squamous epithelium (SqEp).(E-H) Wild-type littermate was LacZ-negative.

Figure 4 .
Figure 4. LacZ expression in the female reproductive system.(A) Cross-section of the ovary of a non-pregnant mouse.LacZ expression is visible in the ovarian follicles and oviduct.(B,C) High magnification of ovarian follicles and oviduct.(D) Section of the vagina with a LacZ signal at the stratified squamous epithelium (SqEp).(E-H) Wild-type littermate was LacZ-negative.

Figure 5 .
Figure 5. LacZ expression in the digestive system.Whole-mount and frozen section showing LacZ signals in the squamous epithelium (SqEp) of the fore stomach (A-C), esophagus (G,H), crypts of the Lieberkühn of the jejunum (K), and dorsal epithelium of the tongue (L).The control, labeled as WT, shows no staining (D-F,I,J).

Figure 6 .
Figure 6.LacZ expression in the respiratory system.(A) Whole-mount staining of the lung.(B) Coronal section of the lung, showing an X-gal signal in the epithelial lining of the bronchioles.(C) X-gal signals in the respiratory epithelium lining of the trachea and squamous epithelium of the larynx (D).

Figure 6 .
Figure 6.LacZ expression in the respiratory system.(A) Whole-mount staining of the lung.(B) Coronal section of the lung, showing an X-gal signal in the epithelial lining of the bronchioles.(C) X-gal signals in the respiratory epithelium lining of the trachea and squamous epithelium of the larynx (D).

Figure 7 .
Figure 7. LacZ expression in the genitourinary system.(A-C) Whole-mount and frozen section LacZ staining of a kidney, showing X-gal signal at the renal pelvis and glomeruli.(D) Frozen section of a urinary bladder, showing LacZ signals in the epithelium.(E) Frozen section of an adrenal gland, showing LacZ staining in the medulla.

Figure 8 .
Figure 8. LacZ expression in the cardiovascular system.(A-D) Whole-mount LacZ staining of the veins collected from the tail, tongue, skin, and esophagus.(E-G) LacZ staining in the heart, showing uniform staining at the atrium and ventricle myocardium.

Figure 7 .
Figure 7. LacZ expression in the genitourinary system.(A-C) Whole-mount and frozen section LacZ staining of a kidney, showing X-gal signal at the renal pelvis and glomeruli.(D) Frozen section of a urinary bladder, showing LacZ signals in the epithelium.(E) Frozen section of an adrenal gland, showing LacZ staining in the medulla.

9 Figure 7 .
Figure 7. LacZ expression in the genitourinary system.(A-C) Whole-mount and frozen section LacZ staining of a kidney, showing X-gal signal at the renal pelvis and glomeruli.(D) Frozen section of a urinary bladder, showing LacZ signals in the epithelium.(E) Frozen section of an adrenal gland, showing LacZ staining in the medulla.

Figure 8 .
Figure 8. LacZ expression in the cardiovascular system.(A-D) Whole-mount LacZ staining of the veins collected from the tail, tongue, skin, and esophagus.(E-G) LacZ staining in the heart, showing uniform staining at the atrium and ventricle myocardium.

Figure 8 .
Figure 8. LacZ expression in the cardiovascular system.(A-D) Whole-mount LacZ staining of the veins collected from the tail, tongue, skin, and esophagus.(E-G) LacZ staining in the heart, showing uniform staining at the atrium and ventricle myocardium.

Figure 9 .
Figure 9. qPCR results for total RNA of 8-week-old tissues.(A) Relative mRNA levels were calculated using the ddCt method.Data shown are representative of at least three independent experiments and expressed as the mean ± SD. (B) Confirmation of the specificity of product produced by qPCR using gel electrophoresis.

Figure 9 .
Figure 9. qPCR results for total RNA of 8-week-old tissues.(A) Relative mRNA levels were calculated using the ddCt method.Data shown are representative of at least three independent experiments and expressed as the mean ± SD. (B) Confirmation of the specificity of product produced by qPCR using gel electrophoresis.

Table 1 .
Summary of expression pattern revealed by X-gal staining of Dip2b tm1a/+ mice.

Table 1 .
Summary of expression pattern revealed by X-gal staining of Dip2b tm1a/+ mice.