首页> 外文期刊>Journal of Virology >Tissue-specific expression of human provirus ERV3 mRNA in human placenta: two of the three ERV3 mRNAs contain human cellular sequences.
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Tissue-specific expression of human provirus ERV3 mRNA in human placenta: two of the three ERV3 mRNAs contain human cellular sequences.

机译:人类胎盘中人类潜灵物ERV3 mRNA的组织特异性表达:三种ERV3 mRNA中的两个含有人细胞序列。

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Three polyadenylated RNAs, 9, 7.3, and 3.5 kilobases long, of a human endogenous retrovirus, ERV3, are abundant in human placental chorion, representing about 0.03 to 0.05% of the total mRNA. We characterized the structure of these mRNAs by Northern blot and S1 nuclease mapping analyses. We found that all three RNAs were spliced mRNAs that lacked 5.9 kilobases of proviral sequence, including the gag gene and most of the pol gene. In contrast to the transcription pattern usual for other retroviruses, the transcription pattern of the ERV3 provirus did not include a genome-length mRNA. All three of the ERV3 mRNAs initiated transcription at the same point in the 5' long terminal repeat (LTR) and contained identical splice junctions in the provirus. The 3.5-kilobase RNA was a typical subgenomic proviral mRNA, with its polyadenylation site in the 3' LTR. The two larger ERV3 mRNAs, however, extended through the polyadenylation site in the 3' LTR and were spliced at a second position approximately 370 nucleotides downstream from the 3' LTR. This finding suggests that when the ERV3 retrovirus integrated at this genomic locus in an ancestor of humans, it integrated within or adjacent to a cellular gene.
机译:人类内源性逆转录病毒ERV3的三种聚酰胺化的RNA,9,7.3和3.5千碱基均为人体胎盘诱饵,其占总mRNA的约0.03至0.05%。我们用Northern印迹和S1核酸酶测绘分析表征了这些MRNA的结构。我们发现,所有三个RNA都是剪接MRNA的MRNA,缺少5.9千碱基序列,包括GAG基因和大部分POL基因。与其他逆转录病毒的转录模式相反,ERV3潜华病毒的转录模式不包括基因组长度mRNA。所有三种ERV3 mRNA在5'长端子重复(LTR)中的同一点处的转录引起的转录,并包含潜水员中的相同接头结。 3.5千碱基RNA是典型的亚基组织荧光法mRNA,其在3'LTR中的聚腺苷酸化位点。然而,两个较大的ERV3 mRNA通过在3'LTR中的多腺苷酸化位点延伸,并且在3'LTR下游的第二位剪接在大约370个核苷酸的第二位置。这一发现表明,当ERV3逆转录病毒在人类祖先的这种基因组基因座中,它集成在细胞基因内或附近。

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