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Genomic Analysis of Sequence-Dependent DNA Curvature in Leishmania

Leishmania major is a flagellated protozoan parasite of medical importance. Like other members of the Trypanosomatidae family, it possesses unique mechanisms of gene expression such as constitutive polycistronic transcription of directional gene clusters, gene amplification, mRNA trans-splicing, and...

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Autores principales: Smircich, Pablo, Forteza, Diego, El-Sayed, Najib M., Garat, Beatriz
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3639952/
https://www.ncbi.nlm.nih.gov/pubmed/23646176
http://dx.doi.org/10.1371/journal.pone.0063068
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author Smircich, Pablo
Forteza, Diego
El-Sayed, Najib M.
Garat, Beatriz
author_facet Smircich, Pablo
Forteza, Diego
El-Sayed, Najib M.
Garat, Beatriz
author_sort Smircich, Pablo
collection PubMed
description Leishmania major is a flagellated protozoan parasite of medical importance. Like other members of the Trypanosomatidae family, it possesses unique mechanisms of gene expression such as constitutive polycistronic transcription of directional gene clusters, gene amplification, mRNA trans-splicing, and extensive editing of mitochondrial transcripts. The molecular signals underlying most of these processes remain under investigation. In order to investigate the role of DNA secondary structure signals in gene expression, we carried out a genome-wide in silico analysis of the intrinsic DNA curvature. The L. major genome revealed a lower frequency of high intrinsic curvature regions as well as inter- and intra- chromosomal distribution heterogeneity, when compared to prokaryotic and eukaryotic organisms. Using a novel method aimed at detecting region-integrated intrinsic curvature (RIIC), high DNA curvature was found to be associated with regions implicated in transcription initiation. Those include divergent strand-switch regions between directional gene clusters and regions linked to markers of active transcription initiation such as acetylated H3 histone, TRF4 and SNAP50. These findings suggest a role for DNA curvature in transcription initiation in Leishmania supporting the relevance of DNA secondary structures signals.
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spelling pubmed-36399522013-05-03 Genomic Analysis of Sequence-Dependent DNA Curvature in Leishmania Smircich, Pablo Forteza, Diego El-Sayed, Najib M. Garat, Beatriz PLoS One Research Article Leishmania major is a flagellated protozoan parasite of medical importance. Like other members of the Trypanosomatidae family, it possesses unique mechanisms of gene expression such as constitutive polycistronic transcription of directional gene clusters, gene amplification, mRNA trans-splicing, and extensive editing of mitochondrial transcripts. The molecular signals underlying most of these processes remain under investigation. In order to investigate the role of DNA secondary structure signals in gene expression, we carried out a genome-wide in silico analysis of the intrinsic DNA curvature. The L. major genome revealed a lower frequency of high intrinsic curvature regions as well as inter- and intra- chromosomal distribution heterogeneity, when compared to prokaryotic and eukaryotic organisms. Using a novel method aimed at detecting region-integrated intrinsic curvature (RIIC), high DNA curvature was found to be associated with regions implicated in transcription initiation. Those include divergent strand-switch regions between directional gene clusters and regions linked to markers of active transcription initiation such as acetylated H3 histone, TRF4 and SNAP50. These findings suggest a role for DNA curvature in transcription initiation in Leishmania supporting the relevance of DNA secondary structures signals. Public Library of Science 2013-04-30 /pmc/articles/PMC3639952/ /pubmed/23646176 http://dx.doi.org/10.1371/journal.pone.0063068 Text en © 2013 Smircich et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Smircich, Pablo
Forteza, Diego
El-Sayed, Najib M.
Garat, Beatriz
Genomic Analysis of Sequence-Dependent DNA Curvature in Leishmania
title Genomic Analysis of Sequence-Dependent DNA Curvature in Leishmania
title_full Genomic Analysis of Sequence-Dependent DNA Curvature in Leishmania
title_fullStr Genomic Analysis of Sequence-Dependent DNA Curvature in Leishmania
title_full_unstemmed Genomic Analysis of Sequence-Dependent DNA Curvature in Leishmania
title_short Genomic Analysis of Sequence-Dependent DNA Curvature in Leishmania
title_sort genomic analysis of sequence-dependent dna curvature in leishmania
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3639952/
https://www.ncbi.nlm.nih.gov/pubmed/23646176
http://dx.doi.org/10.1371/journal.pone.0063068
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