The evolution and genomic landscape of CGB1 and CGB2 genes

被引:33
作者
Hallast, Pille
Rull, Kristiina
Laan, Maris
机构
[1] Univ Tartu, Inst Mol & Cell Biol, Dept Biotechnol, EE-51010 Tartu, Estonia
[2] Univ Tartu, Dept Obstet & Gynecol, EE-50090 Tartu, Estonia
基金
英国惠康基金;
关键词
chorionic gonadotropin beta 1 and 2; gene evolution; polymorphism patterns; putative promoter region; in silico transcription factor binding site prediction;
D O I
10.1016/j.mce.2005.11.049
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The origin of completely novel proteins is a significant question in evolution. The luteinizing hormone (LHB)/chorionic gonadotropin (CGB) gene cluster in humans contains a candidate example of this process. Two genes in this cluster (CGB1 and CGB2) exhibit nucleotide sequence similarity with the other LHB/CGB genes, but as a result of frameshifting are predicted to encode a completely novel protein. Our analysis of these genes from humans and related primates indicates a recent origin in the lineage specific to humans and African great apes. While the function of these genes is not yet known, they are strongly conserved between human and chimpanzee and exhibit three-fold lower diversity than LHB across human populations with no mutations that would disrupt the coding sequence. The 5'-upstream region of CGB1/2 contains most of the promoter sequence of hCG beta plus a novel region proximal to the putative transcription start site. In silico prediction of putative transcription factor binding sites supports the hypothesis that CGB I and CGB2 gene products are expressed in, and may contribute to, implantation and placental development. (c) 2006 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:2 / 11
页数:10
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