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复杂的可变RNA加工产生了意想不到的聚腺苷酸聚合酶同工型多样性。

Complex alternative RNA processing generates an unexpected diversity of poly(A) polymerase isoforms.

作者信息

Zhao W, Manley J L

机构信息

Department of Biological Sciences, Columbia University, New York, NY 10027, USA.

出版信息

Mol Cell Biol. 1996 May;16(5):2378-86. doi: 10.1128/MCB.16.5.2378.

Abstract

Multiple forms of poly(A) polymerase (PAPs I, II, and III) cDNA have previously been isolated from bovine, human, and/or frog cDNA libraries. PAPs I and II are long forms of the enzyme that contain four functional domains: an apparent ribonucleoprotein-type RNA-binding domain, a catalytic region that may be related to the polymerase module, two nuclear localization signals (NLSs I and 2), and a C-terminal Ser/Thr-rich region. PAP III would encode a truncated protein that lacks the NLSs and the S/T-rich region. To investigate further the structure and expression of these forms, we isolated the mouse PAP gene and an intronless pseudogene from a mouse liver genomic library. The structure of the gene indicates that different forms of PAP are produced by alternative splicing (PAPs I and II) or by competition between polyadenylation and splicing (PAP III). The pseudogene appears to reflect yet another form of long PAP, which we call PAP IV. Mouse PAP III and two additional truncated forms, PAPs V and VI, which would be produced by use of poly(A) sites in adjacent introns, were also isolated from a mouse brain cDNA library. RNase protection and reverse transcription-PCR analyses showed that PAP II, V, and VI are expressed in all tissues tested but that PAP I and/or IV and III are tissue specific. However, immunoblot analysis detected only the long forms, raising the possibility that the short-form RNAs are not translated. Purified recombinant baculovirus-expressed PAPs were tested in several in vitro assays, and the short forms were found to be inactive. We discuss the possible significance of this complex expression pattern.

摘要

此前已从牛、人及/或蛙的cDNA文库中分离出多种形式的聚腺苷酸聚合酶(PAP I、II和III)cDNA。PAP I和II是该酶的长形式,包含四个功能结构域:一个明显的核糖核蛋白型RNA结合结构域、一个可能与聚合酶模块相关的催化区域、两个核定位信号(NLS I和2)以及一个富含C末端丝氨酸/苏氨酸的区域。PAP III编码一种截短的蛋白质,缺乏NLS和富含丝氨酸/苏氨酸的区域。为了进一步研究这些形式的结构和表达,我们从小鼠肝脏基因组文库中分离出了小鼠PAP基因和一个无内含子的假基因。该基因的结构表明,不同形式的PAP是通过可变剪接(PAP I和II)或通过聚腺苷酸化和剪接之间的竞争(PAP III)产生的。该假基因似乎反映了长PAP的另一种形式,我们称之为PAP IV。小鼠PAP III以及另外两种截短形式PAP V和PAP VI,它们是通过使用相邻内含子中的聚腺苷酸化位点产生的,也从小鼠脑cDNA文库中分离出来。核糖核酸酶保护分析和逆转录PCR分析表明,PAP II、V和VI在所有测试组织中均有表达,但PAP I和/或IV以及III具有组织特异性。然而,免疫印迹分析仅检测到长形式,这增加了短形式RNA不被翻译的可能性。对纯化的重组杆状病毒表达的PAP进行了几种体外测定,发现短形式无活性。我们讨论了这种复杂表达模式的可能意义。

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本文引用的文献

2
The human U1 snRNP-specific U1A protein inhibits polyadenylation of its own pre-mRNA.
Cell. 1993 Mar 26;72(6):881-92. doi: 10.1016/0092-8674(93)90577-d.
5
Multiple forms of poly(A) polymerases in human cells.
Proc Natl Acad Sci U S A. 1994 Feb 1;91(3):979-83. doi: 10.1073/pnas.91.3.979.
6
Poly(A) polymerase contains multiple functional domains.
Mol Cell Biol. 1994 May;14(5):2946-57. doi: 10.1128/mcb.14.5.2946-2957.1994.
7
RNA14 and RNA15 proteins as components of a yeast pre-mRNA 3'-end processing factor.
Science. 1994 Dec 9;266(5191):1702-5. doi: 10.1126/science.7992054.

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