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Alternative Splicing of CIPK3 Results in Distinct Target Selection to Propagate ABA Signaling in Arabidopsis

Calcium (Ca(2+)) signaling is pivotal in transmission of information in the cell. Various Ca(2+) sensing molecules work to sense and relay the encrypted messages to the intended targets in the cell to maintain this signal transduction. CBL-interacting protein kinases (CIPKs) are crucial components o...

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Autores principales: Sanyal, Sibaji K., Kanwar, Poonam, Samtani, Harsha, Kaur, Kanwaljeet, Jha, Saroj K., Pandey, Girdhar K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5705611/
https://www.ncbi.nlm.nih.gov/pubmed/29225607
http://dx.doi.org/10.3389/fpls.2017.01924
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author Sanyal, Sibaji K.
Kanwar, Poonam
Samtani, Harsha
Kaur, Kanwaljeet
Jha, Saroj K.
Pandey, Girdhar K.
author_facet Sanyal, Sibaji K.
Kanwar, Poonam
Samtani, Harsha
Kaur, Kanwaljeet
Jha, Saroj K.
Pandey, Girdhar K.
author_sort Sanyal, Sibaji K.
collection PubMed
description Calcium (Ca(2+)) signaling is pivotal in transmission of information in the cell. Various Ca(2+) sensing molecules work to sense and relay the encrypted messages to the intended targets in the cell to maintain this signal transduction. CBL-interacting protein kinases (CIPKs) are crucial components of Ca(2+) signal transduction during various abiotic stresses. Although there are intron rich CIPKs in the plant genome but very little has been reported about their alternative splicing. Moreover the physiological significance of this event in the Ca(2+) signaling is still elusive. Therefore in this study, we have selected CIPK3, which has highest number of splice variants amongst Arabidopsis CIPKs. Expression profiling of five splice variants of CIPK3 by qRT-PCR in four Arabidopsis thaliana ecotypes revealed preferential transcript accumulation but similar subcellular localization of the variants and interaction with similar CBLs. ABA and drought treatment resulted in the higher accumulation of the alternately spliced transcripts of CIPK3 in Arabidopsis ecotype Wassilewkija. The transcripts of CIPK3.1 and CIPK3.4 are relatively more induced compared to other alternative splice variants. Out of four splice variants studied, we found CIPK3.1 and CIPK3.2 showing preference for ABR1, a previously reported interactor of CIPK3. We conclude that the differential expression and choice of downstream partner by CIPK3-splice variants might be one of the mechanisms of Ca(2+) mediated preferential regulation of ABA and other stress signals.
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spelling pubmed-57056112017-12-08 Alternative Splicing of CIPK3 Results in Distinct Target Selection to Propagate ABA Signaling in Arabidopsis Sanyal, Sibaji K. Kanwar, Poonam Samtani, Harsha Kaur, Kanwaljeet Jha, Saroj K. Pandey, Girdhar K. Front Plant Sci Plant Science Calcium (Ca(2+)) signaling is pivotal in transmission of information in the cell. Various Ca(2+) sensing molecules work to sense and relay the encrypted messages to the intended targets in the cell to maintain this signal transduction. CBL-interacting protein kinases (CIPKs) are crucial components of Ca(2+) signal transduction during various abiotic stresses. Although there are intron rich CIPKs in the plant genome but very little has been reported about their alternative splicing. Moreover the physiological significance of this event in the Ca(2+) signaling is still elusive. Therefore in this study, we have selected CIPK3, which has highest number of splice variants amongst Arabidopsis CIPKs. Expression profiling of five splice variants of CIPK3 by qRT-PCR in four Arabidopsis thaliana ecotypes revealed preferential transcript accumulation but similar subcellular localization of the variants and interaction with similar CBLs. ABA and drought treatment resulted in the higher accumulation of the alternately spliced transcripts of CIPK3 in Arabidopsis ecotype Wassilewkija. The transcripts of CIPK3.1 and CIPK3.4 are relatively more induced compared to other alternative splice variants. Out of four splice variants studied, we found CIPK3.1 and CIPK3.2 showing preference for ABR1, a previously reported interactor of CIPK3. We conclude that the differential expression and choice of downstream partner by CIPK3-splice variants might be one of the mechanisms of Ca(2+) mediated preferential regulation of ABA and other stress signals. Frontiers Media S.A. 2017-11-24 /pmc/articles/PMC5705611/ /pubmed/29225607 http://dx.doi.org/10.3389/fpls.2017.01924 Text en Copyright © 2017 Sanyal, Kanwar, Samtani, Kaur, Jha and Pandey. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Plant Science
Sanyal, Sibaji K.
Kanwar, Poonam
Samtani, Harsha
Kaur, Kanwaljeet
Jha, Saroj K.
Pandey, Girdhar K.
Alternative Splicing of CIPK3 Results in Distinct Target Selection to Propagate ABA Signaling in Arabidopsis
title Alternative Splicing of CIPK3 Results in Distinct Target Selection to Propagate ABA Signaling in Arabidopsis
title_full Alternative Splicing of CIPK3 Results in Distinct Target Selection to Propagate ABA Signaling in Arabidopsis
title_fullStr Alternative Splicing of CIPK3 Results in Distinct Target Selection to Propagate ABA Signaling in Arabidopsis
title_full_unstemmed Alternative Splicing of CIPK3 Results in Distinct Target Selection to Propagate ABA Signaling in Arabidopsis
title_short Alternative Splicing of CIPK3 Results in Distinct Target Selection to Propagate ABA Signaling in Arabidopsis
title_sort alternative splicing of cipk3 results in distinct target selection to propagate aba signaling in arabidopsis
topic Plant Science
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5705611/
https://www.ncbi.nlm.nih.gov/pubmed/29225607
http://dx.doi.org/10.3389/fpls.2017.01924
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