Ye Lu-yi, Zhao Zhi-min, Wang Ming-hua, Luo Shi-jing, Su Cheng-chang, Zhang Rong-mei, Luo Ze-wei, Wang Jiu-cun
National Key Laboratory of Genetic Engineering, Institute of Genetics, School of Life Sciences, Fudan University, Shanghai 200433, China.
Zhongguo Yi Xue Ke Xue Yuan Xue Bao. 2006 Apr;28(2):219-24.
To screen and identify differentially expressed genes between a fertile patient and another infertile patient who belonged to a large Chinese pedigree affected with androgen insensitivity syndrome (AIS).
We constructed the forward and reversed subtracted libraries using genital skin fibroblasts (GSF), which were obtained from the fertile patient MJ and infertile patient ZGJ, as tester respectively. Candidate clones were screened with colony in situ hybridization, dot blot, and Southern blot analysis step by step and conformed with Northern blot analysis. The potential positive clones were sequenced and the homology of the sequences was analyzed.
The forward and reversed subtracted libraries containing differentially expressed pattern of two GSF cell lines were constructed. Two positive clones identified by Northern blot were obtained in the reversed subtracted library. Eleven candidate clones from the two libraries that failed to hybridize with both RNA populations were obtained simultaneously, which might represent differentially expressed low abundance transcripts. Sequencing results and homology analysis demonstrated that the two positive clones were significantly homologous with the genes of autotaxin-t and calcium binding protein calcyclin (S100A6), respectively.
Two positive clones and eleven clones showing no hybridization signals may represent differentially expressed genes between the two GSFs. This finding may be useful to elucidate the molecular mechanisms leading to phenotypic variation and preserved fertility of the AIS pedigree.
筛选并鉴定一名可育患者与另一名不育患者之间的差异表达基因,这两名患者来自一个患有雄激素不敏感综合征(AIS)的大型中国家系。
我们分别以从可育患者MJ和不育患者ZGJ获取的生殖器皮肤成纤维细胞(GSF)作为测试样本,构建正向和反向消减文库。候选克隆通过菌落原位杂交、斑点印迹和Southern印迹分析逐步筛选,并通过Northern印迹分析进行验证。对潜在的阳性克隆进行测序并分析序列的同源性。
构建了包含两种GSF细胞系差异表达模式的正向和反向消减文库。在反向消减文库中获得了两个经Northern印迹鉴定的阳性克隆。同时从两个文库中获得了11个与两种RNA群体均未杂交的候选克隆,这些克隆可能代表差异表达的低丰度转录本。测序结果和同源性分析表明,这两个阳性克隆分别与自分泌运动因子-t和钙结合蛋白钙周期蛋白(S100A6)的基因具有显著同源性。
两个阳性克隆和11个无杂交信号的克隆可能代表两种GSF之间差异表达的基因。这一发现可能有助于阐明导致AIS家系表型变异和保留生育能力的分子机制。