RNA polyadenylation patterns in the human transcriptome

被引:5
|
作者
Xu, Si-Mei [1 ]
Curry-Hyde, Ashton [1 ]
Sytnyk, Vladimir [1 ]
Janitz, Michael [1 ,2 ]
机构
[1] UNSW Sydney, Sch Biotechnol & Biomol Sci, Sydney, NSW, Australia
[2] Univ Leipzig, Paul Flechsig Inst Brain Res, Leipzig, Germany
关键词
Alternative polyadenylation (APA); mRNA; lncRNA; RNA; Transcriptome; Human; POSTTRANSCRIPTIONAL GENE-REGULATION; ALTERNATIVE POLYADENYLATION; MESSENGER-RNA; GERMLINE VARIANT; 3' UTRS; CLEAVAGE; CANCER; SEQ; LOCALIZATION; HEALTH;
D O I
10.1016/j.gene.2021.146133
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The eukaryotic transcriptome undergoes various post-transcriptional modifications which assists gene expression. Polyadenylation is a molecular process occurring at the 3'-end of the RNA molecule which involves the poly (A) polymerase attaching adenine monophosphate molecules in a chain-like fashion to assemble a poly(A) tail. Multiple RNA isoforms are produced with differing 3'-UTR and exonic compositions through alternative polyadenylation (APA) which enhances the diversification of alternatively spliced mRNA transcripts. To study polyadenylation patterns, novel methods have been developed using short-read and long-read sequencing technologies to analyse the 3'-ends of the transcript. Recent studies have identified unique polyadenylation patterns in different cellular functions, including oncogenic activity, which could prove valuable in the understanding of medical genetics, particularly in the discovery of biomarkers in diseased states. We present a review of current literature reporting on polyadenylation and the biological relevance in the mammalian transcriptome, with a focus on the human transcriptome. Additionally, we have explored the various methods available to detect polyadenylation patterns using second and third generation sequencing technologies.
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页数:8
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