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一个新型人类KRAB锌指基因的转录本包含剪接的Alu序列和内源性逆转录病毒片段。

Transcripts from a novel human KRAB zinc finger gene contain spliced Alu and endogenous retroviral segments.

作者信息

Baban S, Freeman J D, Mager D L

机构信息

Terry Fox Laboratory, University of British Columbia, Vancouver, British Columbia, V5Z1L3, Canada.

出版信息

Genomics. 1996 May 1;33(3):463-72. doi: 10.1006/geno.1996.0221.

Abstract

During the course of an investigation into the potential effects of endogenous retroviruses on adjacent gene expression, we isolated two cDNA clones containing a small sequence segment belonging to the human endogenous retrovirus family, HERV-H. Characterization of the clones revealed that they represent transcripts from a novel KRAB zinc finger gene termed ZNF177. The two cDNA clones differ at their 5' termini and in the presence of a 559-bp internal exon. The clone containing this internal exon has six imperfect zinc finger motifs followed by seven perfect copies of the C2H2 type but has a frame shift between the KRAB domain and the downstream zinc finger region. The smaller clone lacks the six imperfect motifs and has an intact ORF. The 5' putative untranslated regions of both cDNAs contain an 86-bp HERV-H env segment and a segment of an Alu repeat, both in the antisense orientation, that have been incorporated by splicing. RT-PCR experiments show evidence of alternative splicing but the majority of transcripts appear to contain the Alu and env segments. Genomic PCR and hybridization experiments suggest that a partial HERV-H element is integrated within the ZNF177 locus, which Southern analysis has shown to be a single-copy gene. Northern and RT-PCR analyses suggest that ZNF177 is transcribed at a low level in a variety of cell types.

摘要

在对内源逆转录病毒对相邻基因表达的潜在影响进行调查的过程中,我们分离出了两个cDNA克隆,它们包含一段属于人类内源性逆转录病毒家族HERV-H的小序列片段。对这些克隆的表征显示,它们代表了一个名为ZNF177的新型KRAB锌指基因的转录本。这两个cDNA克隆在其5'末端以及一个559 bp的内部外显子的存在上有所不同。包含这个内部外显子的克隆有六个不完美的锌指基序,随后是七个C2H2型的完美拷贝,但在KRAB结构域和下游锌指区域之间存在移码。较小的克隆缺少这六个不完美的基序,并且有一个完整的开放阅读框。两个cDNA的5'推定非翻译区都包含一个86 bp的HERV-H env片段和一个Alu重复序列片段,二者均为反义方向,它们已通过剪接被整合。RT-PCR实验显示了可变剪接的证据,但大多数转录本似乎都包含Alu和env片段。基因组PCR和杂交实验表明,一个部分HERV-H元件整合在ZNF177基因座内,Southern分析表明该基因座是一个单拷贝基因。Northern和RT-PCR分析表明,ZNF177在多种细胞类型中低水平转录。

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