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Dynamics and evolution of the inverted repeat-large single copy junctions in the chloroplast genomes of monocots
BACKGROUND: Various expansions or contractions of inverted repeats (IRs) in chloroplast genomes led to fluxes in the IR-LSC (large single copy) junctions. Previous studies revealed that some monocot IRs contain a trnH-rps19 gene cluster, and it has been speculated that this may be an evidence of a d...
Autores principales: | , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2008
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2275221/ https://www.ncbi.nlm.nih.gov/pubmed/18237435 http://dx.doi.org/10.1186/1471-2148-8-36 |
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author | Wang, Rui-Jiang Cheng, Chiao-Lei Chang, Ching-Chun Wu, Chun-Lin Su, Tian-Mu Chaw, Shu-Miaw |
author_facet | Wang, Rui-Jiang Cheng, Chiao-Lei Chang, Ching-Chun Wu, Chun-Lin Su, Tian-Mu Chaw, Shu-Miaw |
author_sort | Wang, Rui-Jiang |
collection | PubMed |
description | BACKGROUND: Various expansions or contractions of inverted repeats (IRs) in chloroplast genomes led to fluxes in the IR-LSC (large single copy) junctions. Previous studies revealed that some monocot IRs contain a trnH-rps19 gene cluster, and it has been speculated that this may be an evidence of a duplication event prior to the divergence of monocot lineages. Therefore, we compared the organizations of genes flanking two IR-LSC junctions in 123 angiosperm representatives to uncover the evolutionary dynamics of IR-LSC junctions in basal angiosperms and monocots. RESULTS: The organizations of genes flanking IR-LSC junctions in angiosperms can be classified into three types. Generally each IR of monocots contains a trnH-rps19 gene cluster near the IR-LSC junctions, which differs from those in non-monocot angiosperms. Moreover, IRs expanded more progressively in monocots than in non-monocot angiosperms. IR-LSC junctions commonly occurred at polyA tract or A-rich regions in angiosperms. Our RT-PCR assays indicate that in monocot IR(A )the trnH-rps19 gene cluster is regulated by two opposing promoters, S10(A )and psbA. CONCLUSION: Two hypotheses are proposed to account for the evolution of IR expansions in monocots. Based on our observations, the inclusion of a trnH-rps19 cluster in majority of monocot IRs could be reasonably explained by the hypothesis that a DSB event first occurred at IR(B )and led to the expansion of IRs to trnH, followed by a successive DSB event within IR(A )and lead to the expansion of IRs to rps19 or to rpl22 so far. This implies that the duplication of trnH-rps19 gene cluster was prior to the diversification of extant monocot lineages. The duplicated trnH genes in the IR(B )of most monocots and non-monocot angiosperms have distinct fates, which are likely regulated by different expression levels of S10(A )and S10(B )promoters. Further study is needed to unravel the evolutionary significance of IR expansion in more recently diverged monocots. |
format | Text |
id | pubmed-2275221 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-22752212008-03-26 Dynamics and evolution of the inverted repeat-large single copy junctions in the chloroplast genomes of monocots Wang, Rui-Jiang Cheng, Chiao-Lei Chang, Ching-Chun Wu, Chun-Lin Su, Tian-Mu Chaw, Shu-Miaw BMC Evol Biol Research Article BACKGROUND: Various expansions or contractions of inverted repeats (IRs) in chloroplast genomes led to fluxes in the IR-LSC (large single copy) junctions. Previous studies revealed that some monocot IRs contain a trnH-rps19 gene cluster, and it has been speculated that this may be an evidence of a duplication event prior to the divergence of monocot lineages. Therefore, we compared the organizations of genes flanking two IR-LSC junctions in 123 angiosperm representatives to uncover the evolutionary dynamics of IR-LSC junctions in basal angiosperms and monocots. RESULTS: The organizations of genes flanking IR-LSC junctions in angiosperms can be classified into three types. Generally each IR of monocots contains a trnH-rps19 gene cluster near the IR-LSC junctions, which differs from those in non-monocot angiosperms. Moreover, IRs expanded more progressively in monocots than in non-monocot angiosperms. IR-LSC junctions commonly occurred at polyA tract or A-rich regions in angiosperms. Our RT-PCR assays indicate that in monocot IR(A )the trnH-rps19 gene cluster is regulated by two opposing promoters, S10(A )and psbA. CONCLUSION: Two hypotheses are proposed to account for the evolution of IR expansions in monocots. Based on our observations, the inclusion of a trnH-rps19 cluster in majority of monocot IRs could be reasonably explained by the hypothesis that a DSB event first occurred at IR(B )and led to the expansion of IRs to trnH, followed by a successive DSB event within IR(A )and lead to the expansion of IRs to rps19 or to rpl22 so far. This implies that the duplication of trnH-rps19 gene cluster was prior to the diversification of extant monocot lineages. The duplicated trnH genes in the IR(B )of most monocots and non-monocot angiosperms have distinct fates, which are likely regulated by different expression levels of S10(A )and S10(B )promoters. Further study is needed to unravel the evolutionary significance of IR expansion in more recently diverged monocots. BioMed Central 2008-01-31 /pmc/articles/PMC2275221/ /pubmed/18237435 http://dx.doi.org/10.1186/1471-2148-8-36 Text en Copyright ©2008 Wang 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 Wang, Rui-Jiang Cheng, Chiao-Lei Chang, Ching-Chun Wu, Chun-Lin Su, Tian-Mu Chaw, Shu-Miaw Dynamics and evolution of the inverted repeat-large single copy junctions in the chloroplast genomes of monocots |
title | Dynamics and evolution of the inverted repeat-large single copy junctions in the chloroplast genomes of monocots |
title_full | Dynamics and evolution of the inverted repeat-large single copy junctions in the chloroplast genomes of monocots |
title_fullStr | Dynamics and evolution of the inverted repeat-large single copy junctions in the chloroplast genomes of monocots |
title_full_unstemmed | Dynamics and evolution of the inverted repeat-large single copy junctions in the chloroplast genomes of monocots |
title_short | Dynamics and evolution of the inverted repeat-large single copy junctions in the chloroplast genomes of monocots |
title_sort | dynamics and evolution of the inverted repeat-large single copy junctions in the chloroplast genomes of monocots |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2275221/ https://www.ncbi.nlm.nih.gov/pubmed/18237435 http://dx.doi.org/10.1186/1471-2148-8-36 |
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