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The origin and evolution of plant cystatins and their target cysteine proteinases indicate a complex functional relationship
BACKGROUND: Cystatins and their putative targets, the families of cysteine proteinases C1A and C13 play key roles in plants. Comparative genomic analyses are powerful tools to obtain valuable insights into the conservation and evolution of the proteinases and their proteinaceous inhibitors, and coul...
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2008
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2474614/ https://www.ncbi.nlm.nih.gov/pubmed/18616807 http://dx.doi.org/10.1186/1471-2148-8-198 |
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author | Martinez, Manuel Diaz, Isabel |
author_facet | Martinez, Manuel Diaz, Isabel |
author_sort | Martinez, Manuel |
collection | PubMed |
description | BACKGROUND: Cystatins and their putative targets, the families of cysteine proteinases C1A and C13 play key roles in plants. Comparative genomic analyses are powerful tools to obtain valuable insights into the conservation and evolution of the proteinases and their proteinaceous inhibitors, and could aid to elucidate issues concerning the function of these proteins. RESULTS: We have performed an evolutionary comparative analysis of cysteine proteinases C1A and C13 and their putative inhibitors in representative species of different taxonomic groups that appeared during the evolution of the Viridiplantae. The results indicate that whereas C1A cysteine proteinases are present in all taxonomic groups, cystatins and C13 cysteine proteinases are absent in some basal groups. Moreover, gene duplication events have been associated to the increasing structural and functional complexities acquired in land plants. CONCLUSION: Comparative genomic analyses have provided us valuable insights into the conservation and evolution of the cystatin inhibitory family and their putative targets, the cysteine proteinases from families C1A and C13. Functionality of both families of proteins in plants must be the result of a coevolutionary process that might have occurred during the evolution of basal and land plants leading to a complex functional relationship among them. |
format | Text |
id | pubmed-2474614 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-24746142008-07-17 The origin and evolution of plant cystatins and their target cysteine proteinases indicate a complex functional relationship Martinez, Manuel Diaz, Isabel BMC Evol Biol Research Article BACKGROUND: Cystatins and their putative targets, the families of cysteine proteinases C1A and C13 play key roles in plants. Comparative genomic analyses are powerful tools to obtain valuable insights into the conservation and evolution of the proteinases and their proteinaceous inhibitors, and could aid to elucidate issues concerning the function of these proteins. RESULTS: We have performed an evolutionary comparative analysis of cysteine proteinases C1A and C13 and their putative inhibitors in representative species of different taxonomic groups that appeared during the evolution of the Viridiplantae. The results indicate that whereas C1A cysteine proteinases are present in all taxonomic groups, cystatins and C13 cysteine proteinases are absent in some basal groups. Moreover, gene duplication events have been associated to the increasing structural and functional complexities acquired in land plants. CONCLUSION: Comparative genomic analyses have provided us valuable insights into the conservation and evolution of the cystatin inhibitory family and their putative targets, the cysteine proteinases from families C1A and C13. Functionality of both families of proteins in plants must be the result of a coevolutionary process that might have occurred during the evolution of basal and land plants leading to a complex functional relationship among them. BioMed Central 2008-07-10 /pmc/articles/PMC2474614/ /pubmed/18616807 http://dx.doi.org/10.1186/1471-2148-8-198 Text en Copyright ©2008 Martinez and Diaz; 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 Martinez, Manuel Diaz, Isabel The origin and evolution of plant cystatins and their target cysteine proteinases indicate a complex functional relationship |
title | The origin and evolution of plant cystatins and their target cysteine proteinases indicate a complex functional relationship |
title_full | The origin and evolution of plant cystatins and their target cysteine proteinases indicate a complex functional relationship |
title_fullStr | The origin and evolution of plant cystatins and their target cysteine proteinases indicate a complex functional relationship |
title_full_unstemmed | The origin and evolution of plant cystatins and their target cysteine proteinases indicate a complex functional relationship |
title_short | The origin and evolution of plant cystatins and their target cysteine proteinases indicate a complex functional relationship |
title_sort | origin and evolution of plant cystatins and their target cysteine proteinases indicate a complex functional relationship |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2474614/ https://www.ncbi.nlm.nih.gov/pubmed/18616807 http://dx.doi.org/10.1186/1471-2148-8-198 |
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