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酵母端粒酶的生物合成依赖于输入蛋白mtr10。

Biogenesis of yeast telomerase depends on the importin mtr10.

作者信息

Ferrezuelo Francisco, Steiner Barbara, Aldea Martí, Futcher Bruce

机构信息

Department of Molecular Genetics and Microbiology, State University of New York, Stony Brook, New York 11794-5222, USA.

出版信息

Mol Cell Biol. 2002 Sep;22(17):6046-55. doi: 10.1128/MCB.22.17.6046-6055.2002.

Abstract

Telomerase is a ribonucleoprotein particle (RNP) involved in chromosome end replication, but its biogenesis is poorly understood. The RNA component of yeast telomerase (Tlc1) is synthesized as a polyadenylated precursor and then processed to a mature poly(A)- form. We report here that the karyopherin Mtr10p is required for the normal accumulation of mature Tlc1 and its proper localization to the nucleus. Neither TLC1 transcription nor the stability of poly(A)- Tlc1 is significantly affected in mtr10delta cells. Tlc1 was mostly nuclear in a wild-type background, and this localization was not affected by mutations in other telomerase components. Strikingly, in the absence of Mtr10p, Tlc1 was found dispersed throughout the entire cell. Our results are compatible with two alternative models. First, Mtr10p may import a cytoplasmic complex containing Tlc1 and perhaps other components of telomerase, and shuttling of Tlc1 from the nucleus to the cytoplasm and back may be necessary for the biogenesis of telomerase (the "shuttling" model). Second, Mtr10p may be necessary for the nuclear import of some enzyme needed for the nuclear processing and maturation of Tlc1, and in the absence of this maturation, poly(A)+ Tlc1 is aberrantly exported to the cytoplasm (the "processing enzyme" model).

摘要

端粒酶是一种参与染色体末端复制的核糖核蛋白颗粒(RNP),但其生物发生过程却知之甚少。酵母端粒酶的RNA组分(Tlc1)以多聚腺苷酸化前体的形式合成,然后加工成成熟的多聚腺苷酸缺失型(poly(A)- 型)。我们在此报告,核转运蛋白Mtr10p对于成熟Tlc1的正常积累及其在细胞核中的正确定位是必需的。在mtr10δ细胞中,TLC1的转录以及多聚腺苷酸缺失型Tlc1的稳定性均未受到显著影响。在野生型背景下,Tlc1大多位于细胞核中,并且这种定位不受其他端粒酶组分突变的影响。引人注目的是,在缺乏Mtr10p的情况下,Tlc1分散在整个细胞中。我们的结果与两种替代模型相符。第一种,Mtr10p可能导入一个包含Tlc1以及可能的端粒酶其他组分的细胞质复合物,并且Tlc1从细胞核到细胞质再返回的穿梭过程对于端粒酶的生物发生可能是必要的(“穿梭”模型)。第二种,Mtr10p对于Tlc1在细胞核中进行加工和成熟所需的某些酶的核输入可能是必要的,并且在缺乏这种成熟过程的情况下,多聚腺苷酸阳性(poly(A)+)Tlc1会异常地输出到细胞质中(“加工酶”模型)。

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