Humphrey D, Kwiatkowska J, Henske E P, Haines J L, Halley D, van Slegtenhorst M, Kwiatkowski D J
Experimental Medicine Division, Brigham and Women's Hospital, Boston, MA 02115, USA.
Ann Hum Genet. 1997 Jul;61(Pt 4):299-305. doi: 10.1046/j.1469-1809.1997.6140299.x.
RALGDS is a 115 kDa protein which was identified by its ability to enhance guanine nucleotide exchange for the ras family member ral. It also binds to activated ras and rap1, and appears to function as part of a signalling complex in downstream events following rap1 activation. Here we report the identification of full-length cDNA clones for human RALGDS, isolated from a brain cDNA library. The predicted protein has strong sequence homology to rat and murine isoforms of RALGDS in the N- and C-terminal regions, but an internal region (aa 250-380) shows relatively high divergence with only 42% identical amino acid residues. The human RALGDS gene is contained within a 30 kb region of 9q34, approximately 200 kb proximal to the ABO gene, within the current critical region for the tuberous sclerosis gene TSC1. Partial genomic structure was determined; it consists of at least 11 exons. Based upon analysis of Southern blots from 110 TSC patients, genomic DNA SSCP analysis, and RT-PCR analysis which demonstrated RNA expression of both alleles in patients from 9q34-linked TSC families using intragenic polymorphisms, we conclude that RALGDS is not likely to be TSC1.
RALGDS是一种115千道尔顿的蛋白质,它是通过增强ras家族成员ral的鸟嘌呤核苷酸交换能力而被鉴定出来的。它还能与活化的ras和rap1结合,并且在rap1激活后的下游事件中似乎作为信号复合物的一部分发挥作用。在此,我们报告从人脑cDNA文库中分离出的人RALGDS全长cDNA克隆的鉴定结果。预测的蛋白质在N端和C端区域与大鼠和小鼠的RALGDS同工型具有很强的序列同源性,但内部区域(氨基酸250 - 380)显示出相对较高的差异,只有42%的氨基酸残基相同。人RALGDS基因位于9q34的一个30 kb区域内,距离ABO基因约200 kb,在结节性硬化症基因TSC1的当前关键区域内。确定了部分基因组结构;它由至少11个外显子组成。基于对110例结节性硬化症患者的Southern印迹分析、基因组DNA单链构象多态性分析以及逆转录聚合酶链反应分析(该分析利用基因内多态性证明了9q34连锁结节性硬化症家族患者中两个等位基因的RNA表达),我们得出结论,RALGDS不太可能是TSC1。