Cargando…
Selection against tandem splice sites affecting structured protein regions
BACKGROUND: Alternative selection of splice sites in tandem donors and acceptors is a major mode of alternative splicing. Here, we analyzed whether in-frame tandem sites leading to subtle mRNA insertions/deletions of 3, 6, or 9 nucleotides are under natural selection. RESULTS: We found multiple line...
Autores principales: | , , , , |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2008
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2279118/ https://www.ncbi.nlm.nih.gov/pubmed/18366714 http://dx.doi.org/10.1186/1471-2148-8-89 |
_version_ | 1782152056553865216 |
---|---|
author | Hiller, Michael Szafranski, Karol Huse, Klaus Backofen, Rolf Platzer, Matthias |
author_facet | Hiller, Michael Szafranski, Karol Huse, Klaus Backofen, Rolf Platzer, Matthias |
author_sort | Hiller, Michael |
collection | PubMed |
description | BACKGROUND: Alternative selection of splice sites in tandem donors and acceptors is a major mode of alternative splicing. Here, we analyzed whether in-frame tandem sites leading to subtle mRNA insertions/deletions of 3, 6, or 9 nucleotides are under natural selection. RESULTS: We found multiple lines of evidence that the human protein coding sequences are under selection against such in-frame tandem splice events, indicating that these events are often deleterious. The strength of selection is not homogeneous within the coding sequence as protein regions that fold into a fixed 3D structure (intrinsically ordered) are under stronger selection, especially against sites with a strong minor splice site. Investigating structures of functional protein domains, we found that tandem acceptors are preferentially located at the domain surface and outside structural elements such as helices and sheets. Using three-species comparisons, we estimate that more than half of all mutations that create NAGNAG acceptors in the coding region have been eliminated by selection. CONCLUSION: We estimate that ~2,400 introns are under selection against possessing a tandem site. |
format | Text |
id | pubmed-2279118 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-22791182008-04-03 Selection against tandem splice sites affecting structured protein regions Hiller, Michael Szafranski, Karol Huse, Klaus Backofen, Rolf Platzer, Matthias BMC Evol Biol Research Article BACKGROUND: Alternative selection of splice sites in tandem donors and acceptors is a major mode of alternative splicing. Here, we analyzed whether in-frame tandem sites leading to subtle mRNA insertions/deletions of 3, 6, or 9 nucleotides are under natural selection. RESULTS: We found multiple lines of evidence that the human protein coding sequences are under selection against such in-frame tandem splice events, indicating that these events are often deleterious. The strength of selection is not homogeneous within the coding sequence as protein regions that fold into a fixed 3D structure (intrinsically ordered) are under stronger selection, especially against sites with a strong minor splice site. Investigating structures of functional protein domains, we found that tandem acceptors are preferentially located at the domain surface and outside structural elements such as helices and sheets. Using three-species comparisons, we estimate that more than half of all mutations that create NAGNAG acceptors in the coding region have been eliminated by selection. CONCLUSION: We estimate that ~2,400 introns are under selection against possessing a tandem site. BioMed Central 2008-03-21 /pmc/articles/PMC2279118/ /pubmed/18366714 http://dx.doi.org/10.1186/1471-2148-8-89 Text en Copyright ©2008 Hiller et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Hiller, Michael Szafranski, Karol Huse, Klaus Backofen, Rolf Platzer, Matthias Selection against tandem splice sites affecting structured protein regions |
title | Selection against tandem splice sites affecting structured protein regions |
title_full | Selection against tandem splice sites affecting structured protein regions |
title_fullStr | Selection against tandem splice sites affecting structured protein regions |
title_full_unstemmed | Selection against tandem splice sites affecting structured protein regions |
title_short | Selection against tandem splice sites affecting structured protein regions |
title_sort | selection against tandem splice sites affecting structured protein regions |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2279118/ https://www.ncbi.nlm.nih.gov/pubmed/18366714 http://dx.doi.org/10.1186/1471-2148-8-89 |
work_keys_str_mv | AT hillermichael selectionagainsttandemsplicesitesaffectingstructuredproteinregions AT szafranskikarol selectionagainsttandemsplicesitesaffectingstructuredproteinregions AT huseklaus selectionagainsttandemsplicesitesaffectingstructuredproteinregions AT backofenrolf selectionagainsttandemsplicesitesaffectingstructuredproteinregions AT platzermatthias selectionagainsttandemsplicesitesaffectingstructuredproteinregions |