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鉴定脑内A颗粒元件内的一个RNA序列,该序列能够替代Rev介导的1型人类免疫缺陷病毒转录后调控。

Identification of an RNA sequence within an intracisternal-A particle element able to replace Rev-mediated posttranscriptional regulation of human immunodeficiency virus type 1.

作者信息

Tabernero C, Zolotukhin A S, Bear J, Schneider R, Karsenty G, Felber B K

机构信息

Human Retrovirus Pathogenesis Group, National Cancer Institute-Frederick Cancer Research and Development Center, Frederick, Maryland 21702-1201, USA.

出版信息

J Virol. 1997 Jan;71(1):95-101. doi: 10.1128/JVI.71.1.95-101.1997.

Abstract

Human immunodeficiency virus type 1 (HIV-1) replication depends on the posttranscriptional regulation by the viral Rev protein and can be replaced with the posttranscriptional RNA control element (CTE) of the type D simian retroviruses. We have identified a sequence which shares only nucleotide sequences of the internal loops and secondary structure with the CTE and which is part of a novel murine intracisternal-A particle (IAP) retroelement, inserted within the transcribed mouse osteocalcin-related gene. This sequence, named CTE(IAP), can replace the Rev-mediated regulation of HIV-1, hence it is a posttranscriptional regulatory element. Related elements have been identified in other IAPs. These results suggest that insertional mutagenesis can affect gene expression by providing a functional posttranscriptional control element. The CTE(IAP) and CTEs of the type D simian retroviruses represent a novel class of RNA elements characterized by unique sequences within the internal loops which are predicted to represent the interaction site with cellular factor(s). These findings suggest that such elements may be involved in posttranscriptional regulation of cellular mRNAs.

摘要

1型人类免疫缺陷病毒(HIV-1)的复制依赖于病毒Rev蛋白的转录后调控,并且可以被D型猿猴逆转录病毒的转录后RNA控制元件(CTE)所取代。我们鉴定出了一个序列,它与CTE仅在内环的核苷酸序列和二级结构上有共享,并且是一种新型小鼠脑内A颗粒(IAP)逆转录元件的一部分,该元件插入在转录的小鼠骨钙素相关基因内。这个名为CTE(IAP)的序列能够取代Rev介导的HIV-1调控,因此它是一个转录后调控元件。在其他IAP中也鉴定出了相关元件。这些结果表明,插入诱变可以通过提供一个功能性转录后控制元件来影响基因表达。D型猿猴逆转录病毒的CTE(IAP)和CTE代表了一类新型的RNA元件,其特征在于内环内的独特序列,预计这些序列代表与细胞因子的相互作用位点。这些发现表明,此类元件可能参与细胞mRNA的转录后调控。

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