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非洲爪蟾U1小核RNA基因:转录活性基因的特征揭示了主要和次要的重复基因家族。

Xenopus laevis U1 snRNA genes: characterisation of transcriptionally active genes reveals major and minor repeated gene families.

作者信息

Zeller R, Carri M T, Mattaj I W, De Robertis E M

出版信息

EMBO J. 1984 May;3(5):1075-81. doi: 10.1002/j.1460-2075.1984.tb01931.x.

Abstract

Xenopus laevis U1 snRNA genes are found in several different genomic arrangements. The major family of genes is organised in tandem repeats of 1.8 kb. The minor U1-family is much less abundant and is present on 1.2-kb HinfI restriction fragments. In addition there are genomic arrangements present in one or very few copies, which could represent the ends of repeating units. There is no evidence for the presence of U1 pseudogenes in Xenopus. A cluster of U1 snRNA genes consisting of a member of the minor class of U1 snRNA genes and two of the 'rarely represented' genes was cloned. All three genes were expressed upon microinjection into frog oocytes. A fragment containing 149 bp of 5' flanking sequence, the RNA coding sequence, and 27 bp of 3' flanking sequence was shown to be accurately transcribed into U1 snRNA. These oocyte transcripts are assembled into specific U1 snRNPs. Sequence comparison of the regions flanking Xenopus U1 and U2 snRNA genes showed the presence of two blocks of homology, which are also conserved in many other U snRNA genes. One of these blocks is found at position -60 to -50 before the coding sequence, and we discuss its possible role in the correct initiation of transcription. The other is 3' to the coding sequence and may be involved in the accurate production of mature 3' ends in the RNA.

摘要

非洲爪蟾U1 snRNA基因存在于几种不同的基因组排列中。主要基因家族以1.8 kb的串联重复形式组织。次要的U1家族丰度低得多,存在于1.2 kb的HinfI限制片段上。此外,还有以单拷贝或极少数拷贝形式存在的基因组排列,它们可能代表重复单元的末端。没有证据表明非洲爪蟾中存在U1假基因。克隆了一个由次要类U1 snRNA基因的一个成员和两个“罕见”基因组成的U1 snRNA基因簇。将这三个基因显微注射到蛙卵母细胞中后均能表达。一个包含149 bp的5'侧翼序列、RNA编码序列和27 bp的3'侧翼序列的片段被证明能准确转录为U1 snRNA。这些卵母细胞转录本组装成特定的U1 snRNP。非洲爪蟾U1和U2 snRNA基因侧翼区域的序列比较显示存在两个同源区域,在许多其他U snRNA基因中也保守。其中一个区域位于编码序列之前的-60至-50位置,我们讨论了它在转录正确起始中的可能作用。另一个区域在编码序列的3'端,可能参与RNA成熟3'末端的准确产生。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5646/557475/0b11a8a6221d/emboj00309-0155-a.jpg

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