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Architecture and Distribution of Introns in Core Genes of Four Fusarium Species

Removal of introns from transcribed RNA represents a crucial step during the production of mRNA in eukaryotes. Available whole-genome sequences and expressed sequence tags (ESTs) have increased our knowledge of this process and revealed various commonalities among eukaryotes. However, certain aspect...

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Autores principales: Phasha, Mmatshepho M., Wingfield, Brenda D., Coetzee, Martin P. A., Santana, Quentin C., Fourie, Gerda, Steenkamp, Emma T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Genetics Society of America 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5677156/
https://www.ncbi.nlm.nih.gov/pubmed/28993438
http://dx.doi.org/10.1534/g3.117.300344
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author Phasha, Mmatshepho M.
Wingfield, Brenda D.
Coetzee, Martin P. A.
Santana, Quentin C.
Fourie, Gerda
Steenkamp, Emma T.
author_facet Phasha, Mmatshepho M.
Wingfield, Brenda D.
Coetzee, Martin P. A.
Santana, Quentin C.
Fourie, Gerda
Steenkamp, Emma T.
author_sort Phasha, Mmatshepho M.
collection PubMed
description Removal of introns from transcribed RNA represents a crucial step during the production of mRNA in eukaryotes. Available whole-genome sequences and expressed sequence tags (ESTs) have increased our knowledge of this process and revealed various commonalities among eukaryotes. However, certain aspects of intron structure and diversity are taxon-specific, which can complicate the accuracy of in silico gene prediction methods. Using core genes, we evaluated the distribution and architecture of Fusarium circinatum spliceosomal introns, and linked these characteristics to the accuracy of the predicted gene models of the genome of this fungus. We also evaluated intron distribution and architecture in F. verticillioides, F. oxysporum, and F. graminearum, and made comparisons with F. circinatum. Results indicated that F. circinatum and the three other Fusarium species have canonical 5′ and 3′ splice sites, but with subtle differences that are apparently not shared with those of other fungal genera. The polypyrimidine tract of Fusarium introns was also found to be highly divergent among species and genes. Furthermore, the conserved adenosine nucleoside required during the first step of splicing is contained within unique branch site motifs in certain Fusarium introns. Data generated here show that introns of F. circinatum, as well as F. verticillioides, F. oxysporum, and F. graminearum, are characterized by a number of unique features such as the CTHAH and ACCAT motifs of the branch site. Incorporation of such information into genome annotation software will undoubtedly improve the accuracy of gene prediction methods used for Fusarium species and related fungi.
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spelling pubmed-56771562017-11-09 Architecture and Distribution of Introns in Core Genes of Four Fusarium Species Phasha, Mmatshepho M. Wingfield, Brenda D. Coetzee, Martin P. A. Santana, Quentin C. Fourie, Gerda Steenkamp, Emma T. G3 (Bethesda) Investigations Removal of introns from transcribed RNA represents a crucial step during the production of mRNA in eukaryotes. Available whole-genome sequences and expressed sequence tags (ESTs) have increased our knowledge of this process and revealed various commonalities among eukaryotes. However, certain aspects of intron structure and diversity are taxon-specific, which can complicate the accuracy of in silico gene prediction methods. Using core genes, we evaluated the distribution and architecture of Fusarium circinatum spliceosomal introns, and linked these characteristics to the accuracy of the predicted gene models of the genome of this fungus. We also evaluated intron distribution and architecture in F. verticillioides, F. oxysporum, and F. graminearum, and made comparisons with F. circinatum. Results indicated that F. circinatum and the three other Fusarium species have canonical 5′ and 3′ splice sites, but with subtle differences that are apparently not shared with those of other fungal genera. The polypyrimidine tract of Fusarium introns was also found to be highly divergent among species and genes. Furthermore, the conserved adenosine nucleoside required during the first step of splicing is contained within unique branch site motifs in certain Fusarium introns. Data generated here show that introns of F. circinatum, as well as F. verticillioides, F. oxysporum, and F. graminearum, are characterized by a number of unique features such as the CTHAH and ACCAT motifs of the branch site. Incorporation of such information into genome annotation software will undoubtedly improve the accuracy of gene prediction methods used for Fusarium species and related fungi. Genetics Society of America 2017-10-09 /pmc/articles/PMC5677156/ /pubmed/28993438 http://dx.doi.org/10.1534/g3.117.300344 Text en Copyright © 2017 Phasha et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Investigations
Phasha, Mmatshepho M.
Wingfield, Brenda D.
Coetzee, Martin P. A.
Santana, Quentin C.
Fourie, Gerda
Steenkamp, Emma T.
Architecture and Distribution of Introns in Core Genes of Four Fusarium Species
title Architecture and Distribution of Introns in Core Genes of Four Fusarium Species
title_full Architecture and Distribution of Introns in Core Genes of Four Fusarium Species
title_fullStr Architecture and Distribution of Introns in Core Genes of Four Fusarium Species
title_full_unstemmed Architecture and Distribution of Introns in Core Genes of Four Fusarium Species
title_short Architecture and Distribution of Introns in Core Genes of Four Fusarium Species
title_sort architecture and distribution of introns in core genes of four fusarium species
topic Investigations
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5677156/
https://www.ncbi.nlm.nih.gov/pubmed/28993438
http://dx.doi.org/10.1534/g3.117.300344
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