Differential Expression of the KIT Gene in Liaoning Cashmere Goats with different Coat Colors.
KIT encodes a growth factor receptor that is expressed in the precursor of the melanophore. It plays an important role in the multiplication, migration and survival of melanophores. As of yet, no studies have addressed the diverse expression of the KIT gene and its protein in goats of different fur colors. The effect of KIT mutations on KIT protein expression was examined in white cashmere and black cashmere goats. A single AaG missense mutation in exon 13 differentiated cashmere goats with different colors. Only a histidine (H)aarginine (R) amino acid (AA) change was detected at KIT exon 13 in both the white cashmere goat and the black cashmere goat. Moreover, comparison with other species revealed three dramatic amino acid mutation areas.
Our results also indicated that c-kit expression was higher in the white cashmere goat than in the black goat, and this significant difference was detected by q-PCR and western blotting. All cashmere goats of different colors examined by immunohistochemical analysis showed either weak (the black cashmere goat) or strong (the white cashmere goat) expression of the KIT protein. These findings suggested a relationship between mutations in KIT exon 13 and differential fur color in cashmere goats. These results lay the foundation for further research on exon 13 of the KIT gene and color regulation in cashmere goats.
KIT, Melanin, Liaoning Cashmere goat, Mutation, Immunohistochemical.
Coat color is one of the most important breeding traits in horses, goats and other domestic animals (Fontanesi et al., 2011). Among fiber-producing animals, the new breed of Liaoning goats that produce cashmere, also known as "fiber gem", possesses qualities such as high cashmere yield and good cashmere fineness (Kambe et al., 2011). Studies have identified a number of genes that regulate the fur color of cashmere goats. KIT is a type III receptor tyrosine kinase that binds to the ligand MGF and plays a crucial role in the growth and differentiation of melanocytes, hematopoietic cells, and germ cells. The KIT and MGF genes are associated with pigmentation disorders, anemia, sterility and recessive lethality (Besmer et al., 1993; Pawson and Bernstien, 1990). Mutations at the KIT locus can lead to pleiotropic developmental defects in pigment cells, and KIT activation impacts blood cells (Geissler et al., 1988; Haase et al., 2010).
For instance, KIT mutations cause dominant white spotting (KITW) in mice and piebaldism in humans, which both display strikingly similar white patches of hair and skin in heterozygous individuals (Ezoe et al., 1995; Geissler et al., 1988). KIT also plays a pivotal role in melanocyte migration, development and proliferation (Grichnik, 2006). Studies have confirmed the presence of the semidominant IP allele and the dominant I allele in the pig, which are both associated with a duplication of the KIT gene (Johansson-Moller et al., 1996). The white color and the mode of inheritance are controlled by an autosomal dominant allele designated I (KIT) for 'inhibition of color' (Ollivier and Sellier, 1982). The I allele in pigs leads to a complete loss of skin pigmentation. In contrast to murine KIT mutants, homozygous I/I pigs are fully fertile (Marklund et al., 1998). In addition, murine KIT mutations are often homozygous lethal or sublethal.
Dominant white (I) pigs lack mature melanocytes in the skin as well as lacking precursor melanocytes as would be anticipated for a KIT mutation (Johansson-Moller et al., 1996). Hence, KIT expression is related to the prevention of severe pleiotropic effects on other tissues caused by the gene duplication in I/I (KIT). We report the differential expression of KIT in dominant white and black cashmere goats at the gene, protein, tissue and epigenetic levels. The results indicate that three mutation areas exist in exon 13 of KIT, and one of them (159-171 AA) influences the coat color of cashmere goats. Using immunohistochemical analysis, we uncovered the distribution of c-KIT in the skin of cashmere goats. In this study, KIT was selected to investigate the association of polymorphisms with fur color in the cashmere goat.
MATERIALS AND METHODS
Animal experiments were conducted in strict accordance with the guidance for the care and use of laboratory animals by the Jilin University Animal Care and Use Committee (permit number: SYXK (Ji) 2008-0010/0011). All production traits were measured with standardized methods.
Sample collection and RNA extraction
Cashmere goats were acquired from the BaiShang Livestock farm in Changchun, China. The cashmere goats were classified into two groups according to their black or white fur color. A section 5.0 cm in diameter was sheared in the shoulder blade of the goats. The samples were first disinfected in ethanol followed by placement in Hanks solution and taken to the laboratory where they were kept at -80AdegC.
To extract total RNA from the skin, each sample was frozen in liquid nitrogen and ground. The sample was placed into a centrifuge tube containing 1 mL TRIzol reagent and incubated for 5 min followed by the addition of 200 ul chloroform and mixing. The sample was incubated for 10 min and centrifuged at 12000 g for 15 min at 4AdegC. The supernatant was collected in a clean centrifuge tube, and 500 ul isopropanol was added and mixed, incubated for 10 min, and centrifuged at 12000 g for 10 min at 4AdegC. After centrifugation, the supernatant was removed. The sample was washed several times with 1 mL cold 75% ethanol and centrifuged at 7500 g for 5 min at 4AdegC, and the supernatant was discarded. After drying for several minutes, 20 ul DEPC-treated water was added, and the samples were kept at -80AdegC.
The analysis of RT-PCR and cDNA sequencing
Total RNA was extracted using TRIzol reagent (Invitrogen) according to the manufacturer's protocol. RT-PCR was performed for KIT gene exon 13 using an ImProm-II RT system (Promega) according to the manufacturer's instructions. Primers were designed using Primer 5.0 and synthesized by AuGCT Biotechnology Co. The primers were KIT-exon13 (5'-GGYAATCACATGAATAATGTGAA-3') for the forward reaction and KIT-exon13 (5'-TCACCATAGCAACAATATTCTGT-3') for the reverse reaction (GenBank accession MGI: D45168.1). PCR amplifications were performed with a 5 min pre-incubation at 94AdegC followed by 35 cycles of 30 s at 94AdegC and 30 s at 60AdegC. PCR products were veried by melting curve analysis, agarose gel electrophoresis, gel purification and DNA sequencing.
Real-time quantitative reverse transcription-PCR
For real-time quantitative reverse transcription (RT)-PCR, total RNA was reverse transcribed using an ImProm-II RT system (Promega) according to the manufacturer's instructions. For detection and quantication, a MyiQ real-time PCR detection system (Bio-Rad) was used. PCRs were performed using a SYBR Premix Ex Taq II (Takara, Seoul, Republic of Korea). PCRs were carried out in a nal volume of 20 mL using 0.5 mM of each primer, cDNA, and 10 mL of the supplied enzyme mixture containing the DNA double-strand-specic SYBR Green I dye for detection of PCR products. PCRs were performed with a 3 min pre-incubation at 95AdegC followed by 40 cycles of 10 s at 95AdegC and 30 s at 60AdegC. PCR products were veried by melting curve analysis and agarose gel electrophoresis. The standard curve was exported from the MyiQ real-time PCR detection system (Bio-Rad).
The difference in efficiencies was less than 0.1, indicating similar amplification efficiencies of the two cDNAs. The relative amount of mRNA to GAPDH RNA was calculated using the equation 2-IICT where IICT = (ICT mRNA - ICT GAPDH) (Yuan et al., 2006).
Western blotting analysis
Total protein from skin samples from differently colored goats was extracted with Thermo Scientific M-PER Mammalian Protein Extraction Reagent. The protein concentrations were determined using a BCA(tm) protein assay KIT. Aliquots of the lysates were separated on a 10% SDS-polyacrylamide gel and transferred onto a polyvinylidene fluoride (PVDF) membrane (Bio-Rad) with a glycine transfer buffer [192 mM glycine, 25 mM Tris-HCl (pH 8.8), 20% methanol (v/v)]. After blocking nonspecific sites with blocking solution [5% (wt/vol) nonfat dry milk], the membrane was incubated overnight with a specific primary antibody at 4AdegC. The membrane was then incubated for an additional 60 min with a peroxidase-conjugated secondary antibody at room temperature. The immuno-active proteins were detected using an enhanced chemiluminescence (ECL) western blotting detection KIT (Chen et al., 2013).
Epidermis samples from white and black cashmere goats were fixed in formalin-buffered saline and embedded in paraffin. Tissue sections (5 mm) were deparaffinized in xylene for 10 min, dehydrated in alcohol, and rinsed with PBS. For exposure and detection of the KIT protein, antigen retrieval was performed by heating in the microwave in citric acid-sodium citrate for 10 min. Nonspecific binding was blocked by incubating the sections in 10% normal goat serum in Tris-buffered saline for 60 min. We used a rabbit antibody directed against human c-KIT (RandD Systems) at a concentration of 15 ug/ml. Binding was detected using an Cy3-goat-anti-rabbit IgG at a dilution of 1:100 for 40 min. Sections were washed in PBS and subsequently counterstained using DAPI (Haase et al., 2007).
Data are presented as the mean +- SD. Comparison between groups was made with a one-way analysis of variance (ANOVA; Dunnett's t-test) and Student's t-test. P-Values of 0.05 or less were considered statistically significant.
The sequencing analysis indicates that KIT exon 13 has a total length of approximately 1000 bp excluding any introns. According to NCBI, it can translate approximately 333 amino acid residues. A prediction of the secondary structure of the protein which using DNAMAN7.0 coded by KIT exon 13 revealed a random coil, an [alpha]-helix and two transmembrane domains (Fig. 1C-II, 1C-III). The similarity of KIT exon 13 between the white and black goats was found to be up to 99% using DNAMAN7.0 to compare the predicted amino acid sequences. We screened exon 13 of the KIT gene in the dominant white goat and black goat, and identified a single-base AaG point missense mutation in all the samples (Fig. 1A). Only a single histidine (H)aarginine (R) amino acid (AA) difference was detected in exon 13 between the white and black goats.
The change was found in the 159-171 aa area, which is in the second signal transduction extracellular transmembrane domain (Fig. 1B, 1C-I). Moreover, comparison with other species revealed that homology between the white cashmere goat and Capra hircus was 98%, Equus caballus was 70%, Ovis aries was 85% and Bos taurus was 75% (Table I). In goats, amino acid substitutions were detected in the exon 13 coding region of the KIT gene, namely, glutamine (Q)alysine (K) between residues 88-111, tyrosine (Y)aalanine (A) between residues 135-151 and others (Fig. 1B). In addition, both mutations were in transmembrane domains. One mutation is located in the first transmembrane domain and the other on the second transmembrane domain (Fig. 1C-I). Phylogenetic tree analysis revealed that the white cashmere goat has the tightest genetic relationship with the black cashmere goat, comparatively stronger than that between Capra hircus and Ovis aries (Fig. 1C-III).
Table I.- Comparison of the homology of goat KIT-exon13 gene with other mammals at the nt and aa levels (%).
KIT-13###C. hircus###O. aries###B. taurus###E. caballus
Analysis of expression level of KIT exon 13 by qPCR
Real-time RT-PCR analysis of KIT exon 13 mRNA from the skin of goats with different coat colors is shown in Figure 2A. The mRNA expression of KIT exon 13 analyzed by IICT was higher in the skin of white goats than in those with black coats (>6.31-fold) (Fig. 2A). This difference in KIT exon 13 mRNA abundance was significant (p6.31-fold, p2.01-fold, p<0.01) (Fig. 2B). The western blot result for c-KIT was in agreement with the q-PCR results. In conclusion, mRNA and protein expression of c-KIT was higher in the white goat than in the black goat.
KIT also played an important role in the distribution of melanin with goats.
It was reported that Dermal papilla (DP) was located in the center of the hair bulb and the dermal papilla cell (DPC) could induce the regeneration of the follicle (Hardy and Vielkind, 1996). H and E staining of goat skin revealed that a single hair follicle contained many hair bulbs (Fig. 2C). The average number of hair bulbs in the white goat was higher than in the black goat. Therefore, KIT might promote the differentiation of the hair bulbs and the regeneration of the follicle. To better understand the distribution, the immunohistochemical images showed that KIT was widely expressed in the skin of white goats and black goats (Fig. 2D). The staining was mainly located in the upper ORS of the hair follicle. The ORS, which is composed of layers of unpigmented cells, mainly provided a place for the differentiation of the follicular stem cells (Alonso and Fuchs, 2003). This result suggests that KIT has a role in the development of hair follicle stem cells.
This study provides evidence for the likely causative mutation for the dominant white phenotype in goats. We have also discovered that c-KIT has an effect on melanocyte migration, development and proliferation in goats of different coat colors. The implications of these finding clearly suggest that KIT is a key molecule in the regulation of coat color in goats. However, KIT is a large gene, and the missense mutation on KIT exon 13 is not the only mutation that can lead to the white phenotype in goats. Other factors may influence the white phenotype in goats, but these require further research.
This work was supported by Special Foundation for Postdoctor of China Ministry of Education (No. 20100471261), the grants from Jilin Province Natural Science Foundation (Nos.20170101156JC), Special Funds for Scientific Research on Public Causes (201303119), and the grants from the National Natural Science Foundation of China (NSFC) (Nos. 30800807 and 31072097).
Conflict of interest statement
The authors declare that there is no confict of interest that could be perceived as prejudicing the impartiality of the research reported.
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|Publication:||Pakistan Journal of Zoology|
|Date:||Dec 31, 2017|
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