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从HeLa细胞中纯化出的多种形式的聚腺苷酸聚合酶在特定mRNA 3'末端形成过程中发挥作用。

Multiple forms of poly(A) polymerases purified from HeLa cells function in specific mRNA 3'-end formation.

作者信息

Ryner L C, Takagaki Y, Manley J L

机构信息

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

出版信息

Mol Cell Biol. 1989 Oct;9(10):4229-38. doi: 10.1128/mcb.9.10.4229-4238.1989.

Abstract

Poly(A) polymerases (PAPs) from HeLa cell cytoplasmic and nuclear fractions were extensively purified by using a combination of fast protein liquid chromatography and standard chromatographic methods. Several forms of the enzyme were identified, two from the nuclear fraction (NE PAPs I and II) and one from the cytoplasmic fraction (S100 PAP). NE PAP I had chromatographic properties similar to those of S100 PAP, and both enzymes displayed higher activities in the presence of Mn2+ than in the presence of Mg2+, whereas NE PAP II was chromatographically distinct and had approximately equal levels of activity in the presence of Mn2+ and Mg2+. Each of the enzymes, when mixed with other nuclear fractions containing cleavage or specificity factors, was able to reconstitute efficient cleavage and polyadenylation of pre-mRNAs containing an AAUAAA sequence element. The PAPs alone, however, showed no preference for precursors containing an intact AAUAAA sequence over a mutated one, providing further evidence that the PAPs have no intrinsic ability to recognize poly(A) addition sites. Two additional properties of the three enzymes suggest that they are related: sedimentation in glycerol density gradients indicated that the native size of each enzyme is approximately 50 to 60 kilodaltons, and antibodies against a rat hepatoma PAP inhibited the ability of each enzyme to function in AAUAAA-dependent polyadenylation.

摘要

通过使用快速蛋白质液相色谱法和标准色谱法相结合的方法,对来自HeLa细胞质和细胞核组分的多聚腺苷酸聚合酶(PAP)进行了广泛的纯化。鉴定出了几种酶形式,两种来自细胞核组分(NE PAPs I和II),一种来自细胞质组分(S100 PAP)。NE PAP I的色谱特性与S100 PAP相似,并且两种酶在Mn2+存在下的活性均高于在Mg2+存在下的活性,而NE PAP II在色谱上有明显差异,在Mn2+和Mg2+存在下的活性水平大致相等。当将每种酶与含有切割或特异性因子的其他细胞核组分混合时,能够重建对含有AAUAAA序列元件的前体mRNA的有效切割和多聚腺苷酸化。然而,单独的PAPs对含有完整AAUAAA序列的前体与突变的前体没有偏好,这进一步证明PAPs没有识别多聚腺苷酸添加位点的内在能力。这三种酶的另外两个特性表明它们是相关的:在甘油密度梯度中的沉降表明每种酶的天然大小约为50至60千道尔顿,并且针对大鼠肝癌PAP的抗体抑制了每种酶在依赖AAUAAA的多聚腺苷酸化中发挥作用的能力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/16d4/362502/4f60515469ee/molcellb00058-0125-a.jpg

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