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小鼠基因组中剪接体U6 snRNA基因的组织方式。

Organization of spliceosomal U6 snRNA genes in the mouse genome.

作者信息

Yuan Y, Reddy R

机构信息

Department of Pharmacology, Baylor College of Medicine, Houston, Texas 77030.

出版信息

Mol Biol Rep. 1988;13(3):159-64. doi: 10.1007/BF00444312.

Abstract

U6 RNA is an abundant small nuclear RNA (snRNA) required for splicing of pre-mRNAs. In mammalian cells, the genes for U1 to U4 snRNAs consist of multigene families ranging from 10 to 100 copies of real genes per haploid genome, and are transcribed by RNA polymerase II. In contrast, results obtained in this study indicate that U6 RNA, which is transcribed by RNA polymerase II and III, may be coded for in mouse cells by only two genes. These two U6 genes are at least 9 kb apart from each other, and the flanking sequences are highly conserved, indicating that the organization of U6 genes is similar to that observed for other mammalian U-snRNA genes.

摘要

U6 RNA是一种丰富的小核RNA(snRNA),是前体mRNA剪接所必需的。在哺乳动物细胞中,U1至U4 snRNA的基因由多基因家族组成,每个单倍体基因组中有10至100个真实基因拷贝,并由RNA聚合酶II转录。相比之下,本研究获得的结果表明,由RNA聚合酶II和III转录的U6 RNA在小鼠细胞中可能仅由两个基因编码。这两个U6基因彼此相距至少9 kb,侧翼序列高度保守,表明U6基因的组织与其他哺乳动物U-snRNA基因的组织相似。

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