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禽逆转录病毒长末端重复序列(LTR)的核苷酸序列分析:与转座元件的结构相似性

Nucleotide sequence analysis of the long terminal repeat (LTR) of avian retroviruses: structural similarities with transposable elements.

作者信息

Ju G, Skalka A M

出版信息

Cell. 1980 Nov;22(2 Pt 2):379-86. doi: 10.1016/0092-8674(80)90348-7.

Abstract

The nucleotide sequences of the long terminal repeat (LTR) from six independently derived avian retrovirus recombinant DNA clones have been determined. The LTRs from three clones are approximately 350 bp in length and differ only in minor base insertions or substitutions. Three other clones have smaller LTRs, each with a large deletion which ranged from 89 to 161 bp. Sequence comparisons of the six LTRs indicate that there is conservation of sequences derived from the 5' terminus of viral RNA and extensive divergence of the 3'-specific sequences. The LTR sequences were obtained from clones of unintegrated viral DNA. Comparison of these LTRs with the sequence of an integrated Schmidt-Ruppin D provirus deduced previously reveals that two nucleotides present at the terminus of the LTR of the unintegrated DNA are absent in the integrated provirus. Analysis of the nucleotide sequence of the LTR from one clone, lambda RAV2-2, reveals several putative regulatory sites for the initiation and termination of transcription. There are also several structural features of the LTR which are analogous to procaryotic and eucaryotic transposable elements. These structural analogies include the presence of inverted complementary repeats at the termini of the LTR, deletions adjacent to LTR termini, and sequence homologies with transposable and other genetic elements. These observations suggest that the LTR of retroviruses function in the control of gene expression and integration.

摘要

已确定了六个独立衍生的禽逆转录病毒重组DNA克隆的长末端重复序列(LTR)的核苷酸序列。三个克隆的LTR长度约为350 bp,仅在少量碱基插入或替换上有所不同。另外三个克隆的LTR较小,每个都有一个89至161 bp的大缺失。六个LTR的序列比较表明,源自病毒RNA 5'末端的序列具有保守性,而3'特异性序列则存在广泛差异。LTR序列来自未整合的病毒DNA克隆。将这些LTR与先前推导的整合型施密特-鲁平D原病毒的序列进行比较,发现未整合DNA的LTR末端存在的两个核苷酸在整合型原病毒中不存在。对一个克隆λRAV2-2的LTR核苷酸序列分析揭示了几个转录起始和终止的假定调控位点。LTR还有几个结构特征类似于原核和真核转座元件。这些结构相似性包括LTR末端存在反向互补重复序列、LTR末端附近的缺失以及与转座和其他遗传元件的序列同源性。这些观察结果表明,逆转录病毒的LTR在基因表达和整合的控制中起作用。

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