» Articles » PMID: 10570197

In Silico Detection of Control Signals: MRNA 3'-end-processing Sequences in Diverse Species

Overview
Specialty Science
Date 1999 Nov 26
PMID 10570197
Citations 118
Authors
Affiliations
Soon will be listed here.
Abstract

We have investigated mRNA 3'-end-processing signals in each of six eukaryotic species (yeast, rice, arabidopsis, fruitfly, mouse, and human) through the analysis of more than 20,000 3'-expressed sequence tags. The use and conservation of the canonical AAUAAA element vary widely among the six species and are especially weak in plants and yeast. Even in the animal species, the AAUAAA signal does not appear to be as universal as indicated by previous studies. The abundance of single-base variants of AAUAAA correlates with their measured processing efficiencies. As found previously, the plant polyadenylation signals are more similar to those of yeast than to those of animals, with both common content and arrangement of the signal elements. In all species examined, the complete polyadenylation signal appears to consist of an aggregate of multiple elements. In light of these and previous results, we present a broadened concept of 3'-end-processing signals in which no single exact sequence element is universally required for processing. Rather, the total efficiency is a function of all elements and, importantly, an inefficient word in one element can be compensated for by strong words in other elements. These complex patterns indicate that effective tools to identify 3'-end-processing signals will require more than consensus sequence identification.

Citing Articles

Evolutionary dynamics of polyadenylation signals and their recognition strategies in protists.

Sajek M, Bilodeau D, Beer M, Horton E, Miyamoto Y, Velle K Genome Res. 2024; 34(10):1570-1581.

PMID: 39327029 PMC: 11529991. DOI: 10.1101/gr.279526.124.


Delineating yeast cleavage and polyadenylation signals using deep learning.

Stroup E, Ji Z Genome Res. 2024; 34(7):1066-1080.

PMID: 38914436 PMC: 11368178. DOI: 10.1101/gr.278606.123.


Spatially revealed roles for lncRNAs in Drosophila spermatogenesis, Y chromosome function and evolution.

Shao Z, Hu J, Jandura A, Wilk R, Jachimowicz M, Ma L Nat Commun. 2024; 15(1):3806.

PMID: 38714658 PMC: 11076287. DOI: 10.1038/s41467-024-47346-w.


A highly contiguous genome assembly reveals sources of genomic novelty in the symbiotic fungus Rhizophagus irregularis.

Manley B, Lotharukpong J, Barrera-Redondo J, Llewellyn T, Yildirir G, Sperschneider J G3 (Bethesda). 2023; 13(6).

PMID: 36999556 PMC: 10234402. DOI: 10.1093/g3journal/jkad077.


Stress-induced transcriptional readthrough into neighboring genes is linked to intron retention.

Hadar S, Meller A, Saida N, Shalgi R iScience. 2022; 25(12):105543.

PMID: 36505935 PMC: 9732411. DOI: 10.1016/j.isci.2022.105543.


References
1.
Schneider T . Information content of individual genetic sequences. J Theor Biol. 1998; 189(4):427-41. DOI: 10.1006/jtbi.1997.0540. View

2.
Guo Z, Sherman F . 3'-end-forming signals of yeast mRNA. Trends Biochem Sci. 1996; 21(12):477-81. DOI: 10.1016/s0968-0004(96)10057-8. View

3.
Graber J, Cantor C, Mohr S, Smith T . Genomic detection of new yeast pre-mRNA 3'-end-processing signals. Nucleic Acids Res. 1999; 27(3):888-94. PMC: 148262. DOI: 10.1093/nar/27.3.888. View

4.
Takagaki Y, Manley J . RNA recognition by the human polyadenylation factor CstF. Mol Cell Biol. 1997; 17(7):3907-14. PMC: 232243. DOI: 10.1128/MCB.17.7.3907. View

5.
Keller W . mRNA polyadenylation and its coupling to other RNA processing reactions and to transcription. Curr Opin Cell Biol. 1999; 11(3):352-7. DOI: 10.1016/S0955-0674(99)80049-0. View