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果蝇生殖细胞缺失基因小鼠同源物的分子克隆、基因组结构及其在生殖系细胞中的表达

Molecular cloning and genomic organization of mouse homologue of Drosophila germ cell-less and its expression in germ lineage cells.

作者信息

Kimura T, Yomogida K, Iwai N, Kato Y, Nakano T

机构信息

Department of Molecular Cell Biology, Department of Science for Laboratory Animal Experimentation, Research Institute for Microbial Diseases, Osaka University, 3-1, Yamada-oka, Suita-shi, Osaka, 565-0871, Japan.

出版信息

Biochem Biophys Res Commun. 1999 Aug 19;262(1):223-30. doi: 10.1006/bbrc.1999.1160.

Abstract

Primordial germ cells (PGCs) are founder cells of all gametes. A number of genes which control PGCs development have been identified in invertebrates, whereas such genes are by and large unelucidated in mammals. Here we describe cloning, genomic structure and expression of mouse homologue of germ cell-less (gcl) gene which is required for PGCs formation in Drosophila. The mouse gcl shows 34% identity compared with Drosophila gcl protein and contains BTB/POZ domain. The gcl gene consists of 14 exons and spans more than 50 kb. The CpG islands are found around exon 1 of the gene. Putative promoter region contains potential binding sites for various transcription factors. Northern blot analysis showed that its mRNA is highly expressed in adult testis with lower expression in ovary, ES (embryonic stem) cells, and various other organs. In situ hybridization analysis revealed strong expression of the gcl gene in the pachytene stage spermatocytes. The expression was also observed in post-migratory PGCs, but was not apparent in migratory and pre-migratory PGCs. Further studies including gene disruption analysis would provide an important insight into mammalian germ lineage development.

摘要

原始生殖细胞(PGCs)是所有配子的始祖细胞。在无脊椎动物中已鉴定出许多控制PGCs发育的基因,而在哺乳动物中这些基因基本上尚未阐明。在此,我们描述了果蝇中PGCs形成所必需的生殖细胞缺失(gcl)基因的小鼠同源物的克隆、基因组结构及表达情况。小鼠gcl与果蝇gcl蛋白相比具有34%的同一性,并含有BTB/POZ结构域。gcl基因由14个外显子组成,跨越超过50 kb。在该基因的外显子1周围发现了CpG岛。推测的启动子区域包含各种转录因子的潜在结合位点。Northern印迹分析表明,其mRNA在成年睾丸中高度表达,在卵巢、胚胎干细胞(ES)及其他各种器官中的表达较低。原位杂交分析显示,gcl基因在粗线期精母细胞中强烈表达。在迁移后的PGCs中也观察到了这种表达,但在迁移中和迁移前的PGCs中不明显。包括基因敲除分析在内的进一步研究将为哺乳动物生殖系发育提供重要的见解。

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