Nishimura D Y, Purchio A F, Murray J C
Department of Pediatrics, University of Iowa, Iowa City 52242.
Genomics. 1993 Feb;15(2):357-64. doi: 10.1006/geno.1993.1068.
We have identified genetic variation within two human genes, transforming growth factor-beta 2 (TGFB2) and the homeobox gene HB24 (HLX1). Reported here are four human RFLPs and SSCPs for TGFB2 in humans and gorillas. In addition, we describe an RFLP and a SSCP for HLX1. We propose that HLX1 is the human homologue of the mouse homeobox gene Hlx based on extensive sequence homology between the genes and the close proximity of both genes to TGFB2 in their respective species. We also report the chromosomal localization of HLX1 to the long arm of human chromosome 1. Finally, utilizing the polymorphisms described for TGFB2 and HLX1, we have been able to localize these genes within a framework map of the distal long arm of chromosome 1 and to study the linkage relationship between these two genes. Pairwise linkage analysis shows that these two genes are linked, with a recombination fraction of 3.1% and a lod score of 14.49.
我们已经在两个人类基因,即转化生长因子β2(TGFB2)和同源框基因HB24(HLX1)中鉴定出了基因变异。本文报道了人类和大猩猩中TGFB2的四种人类限制性片段长度多态性(RFLP)和单链构象多态性(SSCP)。此外,我们还描述了HLX1的一种RFLP和一种SSCP。基于基因之间广泛的序列同源性以及两个基因在各自物种中与TGFB2的紧密相邻关系,我们提出HLX1是小鼠同源框基因Hlx的人类同源物。我们还报告了HLX1在人类1号染色体长臂上的染色体定位。最后,利用所描述的TGFB2和HLX1的多态性,我们能够将这些基因定位在1号染色体长臂远端的框架图内,并研究这两个基因之间的连锁关系。成对连锁分析表明这两个基因是连锁的,重组率为3.1%,对数优势分数为14.49。