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在 和 中交替多聚腺苷酸化的比较分析。

Comparative analysis of alternative polyadenylation in and .

机构信息

Department of Microbiology, Biochemistry and Molecular Genetics, Rutgers New Jersey Medical School, Newark, New Jersey 07103, USA.

RNA Group, Department of Biochemistry, Université de Sherbrooke, Sherbrooke, Quebec J1E 4K8, Canada.

出版信息

Genome Res. 2017 Oct;27(10):1685-1695. doi: 10.1101/gr.222331.117. Epub 2017 Sep 15.

Abstract

Alternative polyadenylation (APA) is a widespread mechanism that generates mRNA isoforms with distinct properties. Here we have systematically mapped and compared cleavage and polyadenylation sites (PASs) in two yeast species, and Although >80% of the mRNA genes in each species were found to display APA, showed greater 3' UTR size differences among APA isoforms than did PASs in different locations of gene are surrounded with distinct sequences in both species and are often associated with motifs involved in the Nrd1-Nab3-Sen1 termination pathway. In strong motifs surrounding distal PASs lead to higher abundances of long 3' UTR isoforms than short ones, a feature that is opposite in Differences in PAS placement between convergent genes lead to starkly different antisense transcript landscapes between budding and fission yeasts. In both species, short 3' UTR isoforms are more likely to be expressed when cells are growing in nutrient-rich media, although different gene groups are affected in each species. Significantly, 3' UTR shortening in coordinates with up-regulation of expression for genes involved in translation during cell proliferation. Using strains deficient for Pcf11 or Pab2, we show that reduced expression of 3'-end processing factors lengthens 3' UTR, with Pcf11 having a more potent effect than Pab2. Taken together, our data indicate that APA mechanisms in and are largely different: has many of the APA features of higher species, and Pab2 in has a different role in APA regulation than its mammalian homolog, PABPN1.

摘要

可变多聚腺苷酸化 (APA) 是一种广泛存在的机制,可产生具有不同性质的 mRNA 异构体。在这里,我们系统地绘制和比较了两个酵母物种 和 的切割和多聚腺苷酸化位点 (PAS)。尽管每个物种中 >80% 的 mRNA 基因都显示出 APA,但 显示出 APA 异构体之间 3'UTR 大小差异大于 PAS 在基因的不同位置周围的序列在两个物种中都是不同的,并且通常与涉及 Nrd1-Nab3-Sen1 终止途径的基序相关。在 中,远端 PAS 周围的强基序导致长 3'UTR 异构体的丰度高于短异构体,这一特征与 相反。趋同基因之间的 PAS 位置差异导致芽殖酵母和裂殖酵母之间截然不同的反义转录景观。在两个物种中,当细胞在营养丰富的培养基中生长时,短 3'UTR 异构体更有可能表达,尽管每个物种中受影响的基因群不同。重要的是, 中 3'UTR 的缩短与参与细胞增殖过程中翻译的基因表达的上调相协调。使用缺乏 Pcf11 或 Pab2 的 菌株,我们表明 3'末端加工因子的表达减少会使 3'UTR 延长,Pcf11 的作用比 Pab2 更强。总之,我们的数据表明 和 中的 APA 机制在很大程度上是不同的: 具有高等生物的许多 APA 特征,而 中的 Pab2 在 APA 调节中的作用与其哺乳动物同源物 PABPN1 不同。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ecc/5630032/6adb075d78bc/1685f01.jpg

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