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Functional diversity of human protein kinase splice variants marks significant expansion of human kinome

BACKGROUND: Protein kinases are involved in diverse spectrum of cellular processes. Availability of draft version of the human genomic data in the year 2001 enabled recognition of repertoire of protein kinases. However, over the years the human genomic data is being refined and the current release o...

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Autores principales: Anamika, Krishanpal, Garnier, Nicolas, Srinivasan, Narayanaswamy
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2805699/
https://www.ncbi.nlm.nih.gov/pubmed/20028505
http://dx.doi.org/10.1186/1471-2164-10-622
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author Anamika, Krishanpal
Garnier, Nicolas
Srinivasan, Narayanaswamy
author_facet Anamika, Krishanpal
Garnier, Nicolas
Srinivasan, Narayanaswamy
author_sort Anamika, Krishanpal
collection PubMed
description BACKGROUND: Protein kinases are involved in diverse spectrum of cellular processes. Availability of draft version of the human genomic data in the year 2001 enabled recognition of repertoire of protein kinases. However, over the years the human genomic data is being refined and the current release of human genomic data has helped us to recognize a larger repertoire of over 900 human protein kinases represented mainly by splice variants. RESULTS: Many of these identified protein kinases are alternatively spliced products. Interestingly, some of the human kinase splice variants appear to be significantly diverged in terms of their functional properties as represented by incorporation or absence of one or more domains. Many sets of protein kinase splice variants have substantially different domain organization and in a few sets of splice variants kinase domains belong to different subfamilies of kinases suggesting potential participation in different signal transduction pathways. CONCLUSIONS: Addition or deletion of a domain between splice variants of multi-domain kinases appears to be a means of generating differences in the functional features of otherwise similar kinases. It is intriguing that marked sequence diversity within the catalytic regions of some of the splice variant kinases result in kinases belonging to different subfamilies. These human kinase splice variants with different functions might contribute to diversity of eukaryotic cellular signaling.
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spelling pubmed-28056992010-01-13 Functional diversity of human protein kinase splice variants marks significant expansion of human kinome Anamika, Krishanpal Garnier, Nicolas Srinivasan, Narayanaswamy BMC Genomics Research article BACKGROUND: Protein kinases are involved in diverse spectrum of cellular processes. Availability of draft version of the human genomic data in the year 2001 enabled recognition of repertoire of protein kinases. However, over the years the human genomic data is being refined and the current release of human genomic data has helped us to recognize a larger repertoire of over 900 human protein kinases represented mainly by splice variants. RESULTS: Many of these identified protein kinases are alternatively spliced products. Interestingly, some of the human kinase splice variants appear to be significantly diverged in terms of their functional properties as represented by incorporation or absence of one or more domains. Many sets of protein kinase splice variants have substantially different domain organization and in a few sets of splice variants kinase domains belong to different subfamilies of kinases suggesting potential participation in different signal transduction pathways. CONCLUSIONS: Addition or deletion of a domain between splice variants of multi-domain kinases appears to be a means of generating differences in the functional features of otherwise similar kinases. It is intriguing that marked sequence diversity within the catalytic regions of some of the splice variant kinases result in kinases belonging to different subfamilies. These human kinase splice variants with different functions might contribute to diversity of eukaryotic cellular signaling. BioMed Central 2009-12-22 /pmc/articles/PMC2805699/ /pubmed/20028505 http://dx.doi.org/10.1186/1471-2164-10-622 Text en Copyright ©2009 Anamika 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
Anamika, Krishanpal
Garnier, Nicolas
Srinivasan, Narayanaswamy
Functional diversity of human protein kinase splice variants marks significant expansion of human kinome
title Functional diversity of human protein kinase splice variants marks significant expansion of human kinome
title_full Functional diversity of human protein kinase splice variants marks significant expansion of human kinome
title_fullStr Functional diversity of human protein kinase splice variants marks significant expansion of human kinome
title_full_unstemmed Functional diversity of human protein kinase splice variants marks significant expansion of human kinome
title_short Functional diversity of human protein kinase splice variants marks significant expansion of human kinome
title_sort functional diversity of human protein kinase splice variants marks significant expansion of human kinome
topic Research article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2805699/
https://www.ncbi.nlm.nih.gov/pubmed/20028505
http://dx.doi.org/10.1186/1471-2164-10-622
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