Holmes S E, Dombroski B A, Krebs C M, Boehm C D, Kazazian H H
Department of Medicine, Johns Hopkins Hospital, Baltimore, Maryland 21205.
Nat Genet. 1994 Jun;7(2):143-8. doi: 10.1038/ng0694-143.
We have found a 2 kilobase insertion containing a rearranged L1 element in the dystrophin gene of a muscular dystrophy patient. We cloned the precursor of this insertion, the second known active human L1 element. The locus, LRE2, has one allele derived from the patient which matches the insertion sequence exactly. LRE2 has a perfect 13-15 bp target site duplication, two open reading frames, and an unusual 21 bp truncation of the 5' end, suggesting that a slightly truncated element can still retrotranspose. It differs from LRE1 by approximately 0.7%. There is an L1 element at LRE2 on approximately 66% of human chromosomes 1q, and the element is absent from chimpanzee and gorilla genomes. These data demonstrate that multiple active L1 elements exist in the human genome, and that a readthrough transcript of an active element is capable of retrotransposition.
我们在一名肌营养不良患者的肌营养不良蛋白基因中发现了一个2千碱基的插入片段,其中包含一个重排的L1元件。我们克隆了这个插入片段的前体,即第二个已知的活跃人类L1元件。该基因座LRE2有一个来自患者的等位基因,与插入序列完全匹配。LRE2有一个完美的13 - 15碱基对的靶位点重复序列、两个开放阅读框,以及5'端一个不寻常的21碱基对截短,这表明一个略有截短的元件仍能进行逆转座。它与LRE1的差异约为0.7%。在大约66%的人类1号染色体q臂上的LRE2处存在一个L1元件,而黑猩猩和大猩猩基因组中不存在该元件。这些数据表明人类基因组中存在多个活跃的L1元件,并且一个活跃元件的通读转录本能够进行逆转座。