Vinogradova T V, Leppik L P, Nikolaev L G, Akopov S B, Kleiman A M, Senyuta N B, Sverdlov E D
Shemyakin-Ovchinnikov Institute of Bioorganic Chemistry, Moscow 117871, Russia.
Virology. 2001 Nov 10;290(1):83-90. doi: 10.1006/viro.2001.1134.
Solitary long terminal repeats (LTRs) of human endogenous retroviruses (HERVs), tens of thousands of which are spread all over the genome, contain a variety of potential transcription regulatory elements. Information on transcriptional behavior of individual solitary LTRs, however, is limited. We studied the transcriptional activity of several individual HERV-K LTRs in a variety of tissues and cell lines. The RT-PCR technique targeted at specific amplification of the U3 or U5 regions of individual LTRs together with their unique genomic flanks was used to estimate the content of each region in the transcripts. An unequal abundance of the U3 and U5 regions of the transcripts of the same LTR in different cells and tumors was observed. Each LTR is transcribed differently in different cells or tissues, and transcriptional behavior of different LTRs was different in the same cell line or tissue. The transcriptional status of LTRs varies in response to mitogenic and stress factors and in tumor tissues compared to normal counterparts. The LTRs thus seem to be the subjects of specific transcription regulation. The data obtained indicate that an appreciable fraction of the LTRs retained regulatory potential throughout millions of years of evolution and thus may contribute to the overall transcription regulatory network.
人类内源性逆转录病毒(HERV)的单个长末端重复序列(LTR)数以万计,遍布于整个基因组中,包含各种潜在的转录调控元件。然而,关于单个孤立LTR转录行为的信息却很有限。我们研究了几种单个HERV-K LTR在多种组织和细胞系中的转录活性。采用针对单个LTR的U3或U5区域及其独特基因组侧翼进行特异性扩增的RT-PCR技术,来估计转录本中每个区域的含量。在不同细胞和肿瘤中,观察到同一LTR转录本的U3和U5区域丰度不等。每个LTR在不同细胞或组织中的转录方式不同,并且不同LTR在同一细胞系或组织中的转录行为也不同。与正常组织相比,LTR的转录状态在有丝分裂原和应激因素作用下以及在肿瘤组织中会发生变化。因此,LTR似乎是特异性转录调控的对象。所获得的数据表明,相当一部分LTR在数百万年的进化过程中保留了调控潜力,因而可能对整体转录调控网络有贡献。