Shaikh T H, Deininger P L
Department of Biochemistry and Molecular Biology, Louisiana State University Medical Center, New Orleans 70112, USA.
J Mol Evol. 1996 Jan;42(1):15-21. doi: 10.1007/BF00163206.
A recently identified Alu element (Leeflang et al. J. Mol. Evol. 1993, 37:559-565), referred to as the "putative founder of the HS (PV) subfamily," was found to be present at orthologous loci in the human, chimpanzee, gorilla, and gibbon lineages. The evolution of this Alu suggested that it is a source gene in the evolution of Alu family repeats for one of the most recent subfamilies, HS. We have determined that this putative founder of the HS subfamily was not present at the orthologous loci in older primates, including old world and new world monkeys. Thus, this particular Alu locus has only been responsible for the establishment of a very small subfamily of Alu sequences. We have further demonstrated that this putative founder Alu was not responsible for the de novo Alu insertion into the neurofibromatosis-1 gene of an individual causing neurofibromatosis. Our data demonstrate that although the putative founder of the HS subfamily found by Leeflang et al. (1993) probably gave rise to one of the most recent subfamilies of Alu sequences, it has not been very active in retroposition.
最近发现的一个Alu元件(Leeflang等人,《分子进化杂志》,1993年,37卷:559 - 565页),被称为“HS(PV)亚家族的假定创始者”,在人类、黑猩猩、大猩猩和长臂猿谱系的直系同源位点中被发现。这个Alu元件的进化表明,它是Alu家族重复序列中最新的亚家族之一HS进化过程中的一个源基因。我们已经确定,这个HS亚家族的假定创始者在包括旧世界猴和新世界猴在内的较古老灵长类动物的直系同源位点中并不存在。因此,这个特定的Alu位点仅导致了一个非常小的Alu序列亚家族的形成。我们进一步证明,这个假定的创始者Alu并非导致一个个体的神经纤维瘤病1基因发生从头Alu插入从而引发神经纤维瘤病的原因。我们的数据表明,尽管Leeflang等人(1993年)发现的HS亚家族的假定创始者可能产生了Alu序列中最新的亚家族之一,但它在逆转录转座方面并不是很活跃。