Feng Yanping, Peng Xiuli, Li Shijun, Gong Yanzhang
Key Lab of Agricultural Animal Genetics, Breeding and Reproduction of Ministry of Education, Huazhong Agricultural University, Wuhan 430070, China.
Acta Biochim Biophys Sin (Shanghai). 2009 Apr;41(4):285-94. doi: 10.1093/abbs/gmp012.
In chicken, the bipotential embryonic gonad differentiates into either a pair of testes or an ovary, but few genes that underlying the gonadal sex differentiation have been identified and the sex-determination gene is still unknown. To identify more genes involved in chicken sex differentiation, we employed suppression subtractive hybridization to isolate differentially expressed genes between sexes from chicken gonads during a period of E3.5-E6. A total of 152 cDNA clones corresponding to 88 genes (41 from F-M library and 47 from M-F library) were screened using dot-blot analysis. These genes are located mainly on the macrochromosomes (1-5) with five in the sex chromosomes (one in W and four in Z), encoding four dominating molecular categories belonging to enzyme, DNA association, RNA association, and structural protein. Comparing the obtained cDNA sequences with those in chicken EST database, it showed that cDNAs of 32 genes from F-M library and 16 from M-F library have homologs in two reported embryonic gonad cDNA libraries. Quantitative real-time PCR analysis of eight genes involved in epigenetic and transcription regulation showed significantly different expression between sexes of CDK2AP1, SMARCE1, SAP18, SUDS3, and PQBP1 appeared at the early stage in gonad development (E4). Based on the functional comparison of sexual differentially expressed genes, the roles of some putatively important genes including ATP5A1W, CDK2AP1, mitochondrial transcripts, etc. have been analyzed. In conclusion, characterization of isolated genes would provide valuable clues to identify potential candidates involved in genetic mechanisms of chicken sex differentiation and gonad development.
在鸡中,双潜能胚胎性腺会分化为一对睾丸或一个卵巢,但目前仅鉴定出少数几个参与性腺性别分化的基因,性别决定基因仍不清楚。为了鉴定更多参与鸡性别分化的基因,我们采用抑制性消减杂交技术,从E3.5-E6期间的鸡性腺中分离两性之间差异表达的基因。使用斑点杂交分析筛选出了总共152个对应于88个基因的cDNA克隆(41个来自F-M文库,47个来自M-F文库)。这些基因主要位于常染色体(1-5号)上,有5个位于性染色体上(1个在W染色体上,4个在Z染色体上),编码属于酶、DNA结合、RNA结合和结构蛋白的四大主要分子类别。将获得的cDNA序列与鸡EST数据库中的序列进行比较,结果显示F-M文库中的32个基因和M-F文库中的16个基因的cDNA在两个已报道的胚胎性腺cDNA文库中有同源物。对参与表观遗传和转录调控的8个基因进行定量实时PCR分析表明,CDK2AP1、SMARCE1、SAP18、SUDS3和PQBP1在性腺发育早期(E4)两性之间的表达存在显著差异。基于性别差异表达基因的功能比较,分析了一些假定重要基因(包括ATP5A1W、CDK2AP1、线粒体转录本等)的作用。总之,对分离基因的表征将为鉴定参与鸡性别分化和性腺发育遗传机制的潜在候选基因提供有价值的线索。