Steinemann M, Steinemann S
Institut für Genetik, Heinrich-Heine-Universität Düsseldorf, Germany.
Genetics. 1997 Feb;145(2):261-6. doi: 10.1093/genetics/145.2.261.
We have cloned a novel transposable element from the neo-Y chromosome of Drosophila miranda. The size of the element, designated as TRAM, is 3.452 bp, including on both sides long terminal direct repeats (LTRs) of 372 bp, respectively. The element is flanked by a 5-bp target site duplication, ATATG. The putative primer binding site (PBS) for minus-strand priming is complementary to 18 nucleotides of the 3'-end of tRNA(Trp). Data base screens for DNA sequence identities were negative, apart from the sequence motif of the PBS. The deduced amino acid sequence from the large ORF does not reveal identities described for other transposons. In situ hybridizations with TRAM subclones show a biased distribution in the genome, with a massive accumulation of TRAM in the neo-Y chromosome, while the former homologue, the X2 chromosome is devoid of TRAM sites. The enriched occurrence of the TRAM element at the evolving neo-Y chromosome of D.miranda adds compelling evidence in favor of the view that Y chromosome degeneration is driven by the accumulation of transposable elements.
我们从米兰达果蝇的新Y染色体中克隆了一种新型转座元件。该元件名为TRAM,大小为3452 bp,两侧分别有372 bp的长末端正向重复序列(LTRs)。该元件两侧有一个5 bp的靶位点重复序列ATATG。负链引发的假定引物结合位点(PBS)与tRNA(Trp) 3'端的18个核苷酸互补。除PBS的序列基序外,数据库中DNA序列同源性筛选结果均为阴性。从大的开放阅读框推导的氨基酸序列未显示出与其他转座子相同的序列。用TRAM亚克隆进行的原位杂交显示其在基因组中的分布存在偏差,TRAM大量积累在新Y染色体中,而其以前的同源物X2染色体则没有TRAM位点。TRAM元件在不断进化的米兰达果蝇新Y染色体上的富集出现,为Y染色体退化是由转座元件积累驱动这一观点提供了有力证据。