Cargando…

The Minus-End-Directed Kinesin OsDLK Shuttles to the Nucleus and Modulates the Expression of Cold-Box Factor 4

The transition to terrestrial plants was accompanied by a progressive loss of microtubule minus-end-directed dynein motors. Instead, the minus-end-directed class-XIV kinesins expanded considerably, likely related to novel functions. One of these motors, OsDLK (Dual Localisation Kinesin from rice), d...

Descripción completa

Detalles Bibliográficos
Autores principales: Xu, Xiaolu, Hummel, Sabine, Harter, Klaus, Kolukisaoglu, Üner, Riemann, Michael, Nick, Peter
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9181729/
https://www.ncbi.nlm.nih.gov/pubmed/35682970
http://dx.doi.org/10.3390/ijms23116291
_version_ 1784723853799325696
author Xu, Xiaolu
Hummel, Sabine
Harter, Klaus
Kolukisaoglu, Üner
Riemann, Michael
Nick, Peter
author_facet Xu, Xiaolu
Hummel, Sabine
Harter, Klaus
Kolukisaoglu, Üner
Riemann, Michael
Nick, Peter
author_sort Xu, Xiaolu
collection PubMed
description The transition to terrestrial plants was accompanied by a progressive loss of microtubule minus-end-directed dynein motors. Instead, the minus-end-directed class-XIV kinesins expanded considerably, likely related to novel functions. One of these motors, OsDLK (Dual Localisation Kinesin from rice), decorates cortical microtubules but moves into the nucleus in response to cold stress. This analysis of loss-of-function mutants in rice indicates that OsDLK participates in cell elongation during development. Since OsDLK harbours both a nuclear localisation signal and a putative leucin zipper, we asked whether the cold-induced import of OsDLK into the nucleus might correlate with specific DNA binding. Conducting a DPI-ELISA screen with recombinant OsDLKT (lacking the motor domain), we identified the Opaque2 motif as the most promising candidate. This motif is present in the promoter of NtAvr9/Cf9, the tobacco homologue of Cold-Box Factor 4, a transcription factor involved in cold adaptation. A comparative study revealed that the cold-induced accumulation of NtAvr9/Cfp9 was specifically quelled in transgenic BY−2 cells overexpressing OsDLK-GFP. These findings are discussed as a working model, where, in response to cold stress, OsDLK partitions from cortical microtubules at the plasma membrane into the nucleus and specifically modulates the expression of genes involved in cold adaptation.
format Online
Article
Text
id pubmed-9181729
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-91817292022-06-10 The Minus-End-Directed Kinesin OsDLK Shuttles to the Nucleus and Modulates the Expression of Cold-Box Factor 4 Xu, Xiaolu Hummel, Sabine Harter, Klaus Kolukisaoglu, Üner Riemann, Michael Nick, Peter Int J Mol Sci Article The transition to terrestrial plants was accompanied by a progressive loss of microtubule minus-end-directed dynein motors. Instead, the minus-end-directed class-XIV kinesins expanded considerably, likely related to novel functions. One of these motors, OsDLK (Dual Localisation Kinesin from rice), decorates cortical microtubules but moves into the nucleus in response to cold stress. This analysis of loss-of-function mutants in rice indicates that OsDLK participates in cell elongation during development. Since OsDLK harbours both a nuclear localisation signal and a putative leucin zipper, we asked whether the cold-induced import of OsDLK into the nucleus might correlate with specific DNA binding. Conducting a DPI-ELISA screen with recombinant OsDLKT (lacking the motor domain), we identified the Opaque2 motif as the most promising candidate. This motif is present in the promoter of NtAvr9/Cf9, the tobacco homologue of Cold-Box Factor 4, a transcription factor involved in cold adaptation. A comparative study revealed that the cold-induced accumulation of NtAvr9/Cfp9 was specifically quelled in transgenic BY−2 cells overexpressing OsDLK-GFP. These findings are discussed as a working model, where, in response to cold stress, OsDLK partitions from cortical microtubules at the plasma membrane into the nucleus and specifically modulates the expression of genes involved in cold adaptation. MDPI 2022-06-03 /pmc/articles/PMC9181729/ /pubmed/35682970 http://dx.doi.org/10.3390/ijms23116291 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Xu, Xiaolu
Hummel, Sabine
Harter, Klaus
Kolukisaoglu, Üner
Riemann, Michael
Nick, Peter
The Minus-End-Directed Kinesin OsDLK Shuttles to the Nucleus and Modulates the Expression of Cold-Box Factor 4
title The Minus-End-Directed Kinesin OsDLK Shuttles to the Nucleus and Modulates the Expression of Cold-Box Factor 4
title_full The Minus-End-Directed Kinesin OsDLK Shuttles to the Nucleus and Modulates the Expression of Cold-Box Factor 4
title_fullStr The Minus-End-Directed Kinesin OsDLK Shuttles to the Nucleus and Modulates the Expression of Cold-Box Factor 4
title_full_unstemmed The Minus-End-Directed Kinesin OsDLK Shuttles to the Nucleus and Modulates the Expression of Cold-Box Factor 4
title_short The Minus-End-Directed Kinesin OsDLK Shuttles to the Nucleus and Modulates the Expression of Cold-Box Factor 4
title_sort minus-end-directed kinesin osdlk shuttles to the nucleus and modulates the expression of cold-box factor 4
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9181729/
https://www.ncbi.nlm.nih.gov/pubmed/35682970
http://dx.doi.org/10.3390/ijms23116291
work_keys_str_mv AT xuxiaolu theminusenddirectedkinesinosdlkshuttlestothenucleusandmodulatestheexpressionofcoldboxfactor4
AT hummelsabine theminusenddirectedkinesinosdlkshuttlestothenucleusandmodulatestheexpressionofcoldboxfactor4
AT harterklaus theminusenddirectedkinesinosdlkshuttlestothenucleusandmodulatestheexpressionofcoldboxfactor4
AT kolukisaogluuner theminusenddirectedkinesinosdlkshuttlestothenucleusandmodulatestheexpressionofcoldboxfactor4
AT riemannmichael theminusenddirectedkinesinosdlkshuttlestothenucleusandmodulatestheexpressionofcoldboxfactor4
AT nickpeter theminusenddirectedkinesinosdlkshuttlestothenucleusandmodulatestheexpressionofcoldboxfactor4
AT xuxiaolu minusenddirectedkinesinosdlkshuttlestothenucleusandmodulatestheexpressionofcoldboxfactor4
AT hummelsabine minusenddirectedkinesinosdlkshuttlestothenucleusandmodulatestheexpressionofcoldboxfactor4
AT harterklaus minusenddirectedkinesinosdlkshuttlestothenucleusandmodulatestheexpressionofcoldboxfactor4
AT kolukisaogluuner minusenddirectedkinesinosdlkshuttlestothenucleusandmodulatestheexpressionofcoldboxfactor4
AT riemannmichael minusenddirectedkinesinosdlkshuttlestothenucleusandmodulatestheexpressionofcoldboxfactor4
AT nickpeter minusenddirectedkinesinosdlkshuttlestothenucleusandmodulatestheexpressionofcoldboxfactor4