首页|汶上芦花鸡CDKN2A基因序列变异、生物信息学及组织表达分析

汶上芦花鸡CDKN2A基因序列变异、生物信息学及组织表达分析

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为检测汶上芦花鸡CDKN2A基因SNP位点,并对该基因进行生物信息学及其在皮肤组织中的表达规律分析。研究基于江苏省家禽科学研究所资源保护与评价课题组前期组装的汶上芦花鸡高质量染色体水平基因组,将其与鸡参考基因组(GRCg7b)比对获得CDKN2A基因SNP位点,采用 MassARRAY核酸质谱技术对其进行多态性检测和基因分型;运用生物信息学软件预测CDKN2A基因调控序列,及其编码蛋白质理化性质和结构特征;采用转录组和实时荧光定量方法分析该基因在汶上芦花鸡不同时期皮肤组织中的表达情况。结果表明,汶上芦花鸡CDKN2A序列总长度为9。854 kb,CDS全长183 bp,共编码60个氨基酸,在该基因及其上下游1 kb序列范围内共发现41个SNP,其中4个为新发现的SNP,分别位于基因下游和内含子区,第1外显子上发现2个错义SNP:V9D和C10R,41个SNP中34个SNP在汶上芦花鸡群体中检出率在91%以上,但基本均为纯合突变型,无多态存在;汶上芦花鸡CDKN2A基因上游2 kb区域内预测到8个启动子和5个CpG岛,启动子区包含Sp1、MEB-1、YY1、C/EBPα和AP-2α等12种转录因子结合潜在位点,该基因编码蛋白分子质量为7。30 ku,理论等电点为12。82,为带正电荷的、不稳定亲水性蛋白,亚细胞定位主要在线粒体中,无信号肽区域和信号肽剪切位点,共存在8个潜在磷酸化位点,不存在糖基化位点,含有典型的TRP_2(瞬时受体电位离子通道Ⅱ)保守结构域,其二级和三级结构主要以α-螺旋和无规则卷曲为主,并与MDM2、NPM1、USP36蛋白存在相互作用;汶上芦花鸡1~35日龄CDKN2A基因在其背部皮肤中的表达呈上升趋势。
Variations,Bioinformatics and Tissue Expression of CDKN2A Gene in Wenshang Barred Chicken
This study aimed to detect the SNPs of CDKN2A gene in Wenshang Barred chicken,and perform the analysis of its bioinformatics and expressions in skin tissues.Based on the high quality chromosome-level genome of Wenshang Barred chicken assembled by the research group of Resource Conservation and Evaluation in Jiangsu In-stitute of Poultry Science,the sequences were blasted to chicken reference genome(GRCg7b)and the SNPs were acquired.These SNPs were detected and genotyped by MassARRAY nucleic acid mass spectrometry in the chicken population.Bioinformatics software was used to predict the regulatory sequence of CDKN2A gene.The physicochemi-cal properties and structural characteristics of the encoded protein were analyzed.The expressions of this gene in the skin tissues of Wenshang Barred chicken at different periods were detected by transcriptome and Real-Time Fluores-cence Quantitative PCR.The results showed that the total length of CDKN2A and its CDS were respectively 9.854 kb and 183 bp,encoding 60 amino acids.Forty-one SNPs were found in this gene and its upstream and downstream 1 kb,of which four SNPs were newly discovered loci.These four new SNPs were located in the down-stream and the intron,respectively.The first exon had two SNPs,both of which were missense mutations:V9D and C10R.The detection rates of 34 SNPs among the 41 SNPs were all over 91%in the Wenshang Barred chicken pop-ulation.These SNPs were almost homozygous mutants without polymorphism.Eight promoters and five CpG islands were predicted in the 2 kb upstream of CDKN2A in Wenshang Barred chicken.The promoter region contained a total of 12 transcription factor binding sites,including Sp1,MEB-1,YY1,C/EBPα,AP-2α.The protein encoded by this gene was a positively charged,unstable hydrophilic protein with a molecular mass of 7.30 ku and a theoretical isoe-lectric point of 12.82.The predictive subcellular localization of the protein was mainly in mitochondria.The protein had no signal peptide regions and signal peptide shear sites.It had eight potential phosphorylation sites and no gly-cosylation sites.The protein contained a typical TRP_2(transient receptor potential ion channel Ⅱ)conserved do-main and its secondary and tertiary structures were mainly α-helices and random coil.In addition,it had interactions with MDM2,NPM1,USP36 proteins.The expressions of CDKN2A gene in the back skins increased from 1 to 35 days old in Wenshang Barred chicken.

Wenshang Barred chickenCDKN2ASNP variationsBioinformatics analysisTissue expression

薛倩、李国辉、周成浩、蒋一秀、邢伟杰、韩威

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江苏省家禽科学研究所科技创新有限公司,江苏扬州 225125

江苏省家禽科学研究所,江苏扬州 225125

汶上芦花鸡 CDKN2A SNP变异位点 生物信息学分析 组织表达

江苏省自然科学基金面上项目江苏省种业振兴"揭榜挂帅"项目国家重点研发计划"农业生物种质资源挖掘与创新利用"重点专项

BK20221285JBGS[2021]0292021YFD1200803

2024

华北农学报
河北,北京,天津,山西,河南,内蒙古六省市农科院农学会

华北农学报

CSTPCD北大核心
影响因子:1.067
ISSN:1000-7091
年,卷(期):2024.39(5)