Huntriss J, Gosden R, Hinkins M, Oliver B, Miller D, Rutherford A J, Picton H M
Academic Unit of Paediatrics, Obstetrics and Gynaecology, University of Leeds, D Floor, Clarendon Wing, Leeds General Infirmary, Belmont Grove, Leeds LS2 9NS, UK.
Mol Hum Reprod. 2002 Dec;8(12):1087-95. doi: 10.1093/molehr/8.12.1087.
The Factor In the Germline alpha (FIGalpha) transcription factor regulates expression of the zona pellucida proteins ZP1, ZP2 and ZP3 and is essential for folliculogenesis in the mouse. Using the published mouse Figla sequence, BLAST searches identified a human chromosome 2 BAC clone with high sequence identity. Using PCR primers derived from this clone, amplicons derived from ovarian follicles and mature oocytes revealed 100% identity with the appropriate human BAC clone, the expected homology with the mouse Figla gene sequence, and homology on translation with the FIGalpha protein identified in the Japanese rice fish, medaka (Oryzias latipes). PCR expression profiling of this transcript revealed FIGLA mRNA expression in cDNA derived from ovarian follicles (5/5 samples from the primordial through to the secondary stage) mature oocytes (6/9 samples), and less frequently in preimplantation embryos (2/7 samples). Subsequent BLAST searches revealed the predicted full length coding sequence of the human FIGalpha protein which demonstrates 68 and 25% similarity overall to mouse and medaka proteins respectively, with 96 and 57% identity respectively within the basic helix-loop-helix region. This confirms our identification of the human homologue for this gene which maps to chromosome 2p12. Further work is required to understand its role in normal human oocyte development and the potential involvement in human infertility.
生殖系α因子(FIGα)转录因子调节透明带蛋白ZP1、ZP2和ZP3的表达,对小鼠卵泡发生至关重要。利用已发表的小鼠Figla序列,通过BLAST搜索鉴定出一个与该序列具有高度同一性的人类2号染色体BAC克隆。使用从该克隆衍生的PCR引物,从卵巢卵泡和成熟卵母细胞获得的扩增子与相应的人类BAC克隆具有100%的同一性,与小鼠Figla基因序列具有预期的同源性,并且在翻译水平上与在日本青鳉(Oryzias latipes)中鉴定的FIGα蛋白具有同源性。对该转录本的PCR表达谱分析显示,FIGLA mRNA在来自卵巢卵泡(从原始卵泡到次级卵泡阶段的5/5个样本)、成熟卵母细胞(6/9个样本)的cDNA中表达,而在植入前胚胎中表达较少(2/7个样本)。随后的BLAST搜索揭示了人类FIGα蛋白的预测全长编码序列,该序列与小鼠和青鳉蛋白的总体相似性分别为68%和25%,在碱性螺旋-环-螺旋区域内的同一性分别为96%和57%。这证实了我们对该基因人类同源物的鉴定,该同源物定位于2号染色体p12区域。需要进一步开展工作以了解其在正常人类卵母细胞发育中的作用以及与人类不孕症的潜在关联。