RNA polyadenylation sites on the genomes of microorganisms, animals, and plants.

Pre-messenger RNA (mRNA) 3'-end cleavage and subsequent polyadenylation strongly regulate gene expression. In comparison with the upstream or downstream motifs, relatively little is known about the feature differences of polyadenylation [poly(A)] sites among major kingdoms. We suspect that the...

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Main Authors: Xiu-Qing Li, Donglei Du
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2013-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3832601?pdf=render
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author Xiu-Qing Li
Donglei Du
author_facet Xiu-Qing Li
Donglei Du
author_sort Xiu-Qing Li
collection DOAJ
description Pre-messenger RNA (mRNA) 3'-end cleavage and subsequent polyadenylation strongly regulate gene expression. In comparison with the upstream or downstream motifs, relatively little is known about the feature differences of polyadenylation [poly(A)] sites among major kingdoms. We suspect that the precise poly(A) sites are very selective, and we therefore mapped mRNA poly(A) sites on complete and nearly complete genomes using mRNA sequences available in the National Center for Biotechnology Information (NCBI) Nucleotide database. In this paper, we describe the mRNA nucleotide [i.e., the poly(A) tail attachment position] that is directly in attachment with the poly(A) tail and the pre-mRNA nucleotide [i.e., the poly(A) tail starting position] that corresponds to the first adenosine of the poly(A) tail in the 29 most-mapped species (2 fungi, 2 protists, 18 animals, and 7 plants). The most representative pre-mRNA dinucleotides covering these two positions were UA, CA, and GA in 17, 10, and 2 of the species, respectively. The pre-mRNA nucleotide at the poly(A) tail starting position was typically an adenosine [i.e., A-type poly(A) sites], sometimes a uridine, and occasionally a cytidine or guanosine. The order was U>C>G at the attachment position but A>>U>C≥G at the starting position. However, in comparison with the mRNA nucleotide composition (base composition), the poly(A) tail attachment position selected C over U in plants and both C and G over U in animals, in both A-type and non-A-type poly(A) sites. Animals, dicot plants, and monocot plants had clear differences in C/G ratios at the poly(A) tail attachment position of the non-A-type poly(A) sites. This study of poly(A) site evolution indicated that the two positions within poly(A) sites had distinct nucleotide compositions and were different among kingdoms.
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spelling doaj.art-3ed86decebaa4505a58552fd87a70ee72022-12-21T20:20:14ZengPublic Library of Science (PLoS)PLoS ONE1932-62032013-01-01811e7951110.1371/journal.pone.0079511RNA polyadenylation sites on the genomes of microorganisms, animals, and plants.Xiu-Qing LiDonglei DuPre-messenger RNA (mRNA) 3'-end cleavage and subsequent polyadenylation strongly regulate gene expression. In comparison with the upstream or downstream motifs, relatively little is known about the feature differences of polyadenylation [poly(A)] sites among major kingdoms. We suspect that the precise poly(A) sites are very selective, and we therefore mapped mRNA poly(A) sites on complete and nearly complete genomes using mRNA sequences available in the National Center for Biotechnology Information (NCBI) Nucleotide database. In this paper, we describe the mRNA nucleotide [i.e., the poly(A) tail attachment position] that is directly in attachment with the poly(A) tail and the pre-mRNA nucleotide [i.e., the poly(A) tail starting position] that corresponds to the first adenosine of the poly(A) tail in the 29 most-mapped species (2 fungi, 2 protists, 18 animals, and 7 plants). The most representative pre-mRNA dinucleotides covering these two positions were UA, CA, and GA in 17, 10, and 2 of the species, respectively. The pre-mRNA nucleotide at the poly(A) tail starting position was typically an adenosine [i.e., A-type poly(A) sites], sometimes a uridine, and occasionally a cytidine or guanosine. The order was U>C>G at the attachment position but A>>U>C≥G at the starting position. However, in comparison with the mRNA nucleotide composition (base composition), the poly(A) tail attachment position selected C over U in plants and both C and G over U in animals, in both A-type and non-A-type poly(A) sites. Animals, dicot plants, and monocot plants had clear differences in C/G ratios at the poly(A) tail attachment position of the non-A-type poly(A) sites. This study of poly(A) site evolution indicated that the two positions within poly(A) sites had distinct nucleotide compositions and were different among kingdoms.http://europepmc.org/articles/PMC3832601?pdf=render
spellingShingle Xiu-Qing Li
Donglei Du
RNA polyadenylation sites on the genomes of microorganisms, animals, and plants.
PLoS ONE
title RNA polyadenylation sites on the genomes of microorganisms, animals, and plants.
title_full RNA polyadenylation sites on the genomes of microorganisms, animals, and plants.
title_fullStr RNA polyadenylation sites on the genomes of microorganisms, animals, and plants.
title_full_unstemmed RNA polyadenylation sites on the genomes of microorganisms, animals, and plants.
title_short RNA polyadenylation sites on the genomes of microorganisms, animals, and plants.
title_sort rna polyadenylation sites on the genomes of microorganisms animals and plants
url http://europepmc.org/articles/PMC3832601?pdf=render
work_keys_str_mv AT xiuqingli rnapolyadenylationsitesonthegenomesofmicroorganismsanimalsandplants
AT dongleidu rnapolyadenylationsitesonthegenomesofmicroorganismsanimalsandplants