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BRXL4‐LAZY1 interaction at the plasma membrane controls Arabidopsis branch angle and gravitropism

Gravitropism guides growth to shape plant architecture above and below ground. Mutations in LAZY1 impair stem gravitropism and cause less upright inflorescence branches (wider angles). The LAZY1 protein resides at the plasma membrane and in the nucleus. The plasma membrane pool is necessary and suff...

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Autores principales: Che, Ximing, Splitt, Bessie L., Eckholm, Magnus T., Miller, Nathan D., Spalding, Edgar P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10107345/
https://www.ncbi.nlm.nih.gov/pubmed/36478485
http://dx.doi.org/10.1111/tpj.16055
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author Che, Ximing
Splitt, Bessie L.
Eckholm, Magnus T.
Miller, Nathan D.
Spalding, Edgar P.
author_facet Che, Ximing
Splitt, Bessie L.
Eckholm, Magnus T.
Miller, Nathan D.
Spalding, Edgar P.
author_sort Che, Ximing
collection PubMed
description Gravitropism guides growth to shape plant architecture above and below ground. Mutations in LAZY1 impair stem gravitropism and cause less upright inflorescence branches (wider angles). The LAZY1 protein resides at the plasma membrane and in the nucleus. The plasma membrane pool is necessary and sufficient for setting branch angles. To investigate the molecular mechanism of LAZY1 function, we screened for LAZY1‐interacting proteins in yeast. We identified BRXL4, a shoot‐specific protein related to BREVIS RADIX. The BRXL4‐LAZY1 interaction occurred at the plasma membrane in plant cells, and not detectably in the nucleus. Mutations in the C‐terminus of LAZY1, but not other conserved regions, prevented the interaction. Opposite to lazy1, brxl4 mutants displayed faster gravitropism and more upright branches. Overexpressing BRXL4 produced strong lazy1 phenotypes. The apparent negative regulation of LAZY1 function is consistent with BRXL4 reducing LAZY1 expression or the amount of LAZY1 at the plasma membrane. Measurements indicated that both are true. LAZY1 mRNA was three‐fold more abundant in brxl4 mutants and almost undetectable in BRXL4 overexpressors. Plasma membrane LAZY1 was higher and nuclear LAZY1 lower in brxl4 mutants compared with the wild type. To explain these results, we suggest that BRXL4 reduces the amount of LAZY1 at the plasma membrane where it functions in gravity signaling and promotes LAZY1 accumulation in the nucleus where it reduces LAZY1 expression, possibly by suppressing its own transcription. This explanation of how BRXL4 negatively regulates LAZY1 suggests ways to modify shoot system architecture for practical purposes.
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spelling pubmed-101073452023-04-18 BRXL4‐LAZY1 interaction at the plasma membrane controls Arabidopsis branch angle and gravitropism Che, Ximing Splitt, Bessie L. Eckholm, Magnus T. Miller, Nathan D. Spalding, Edgar P. Plant J Original Articles Gravitropism guides growth to shape plant architecture above and below ground. Mutations in LAZY1 impair stem gravitropism and cause less upright inflorescence branches (wider angles). The LAZY1 protein resides at the plasma membrane and in the nucleus. The plasma membrane pool is necessary and sufficient for setting branch angles. To investigate the molecular mechanism of LAZY1 function, we screened for LAZY1‐interacting proteins in yeast. We identified BRXL4, a shoot‐specific protein related to BREVIS RADIX. The BRXL4‐LAZY1 interaction occurred at the plasma membrane in plant cells, and not detectably in the nucleus. Mutations in the C‐terminus of LAZY1, but not other conserved regions, prevented the interaction. Opposite to lazy1, brxl4 mutants displayed faster gravitropism and more upright branches. Overexpressing BRXL4 produced strong lazy1 phenotypes. The apparent negative regulation of LAZY1 function is consistent with BRXL4 reducing LAZY1 expression or the amount of LAZY1 at the plasma membrane. Measurements indicated that both are true. LAZY1 mRNA was three‐fold more abundant in brxl4 mutants and almost undetectable in BRXL4 overexpressors. Plasma membrane LAZY1 was higher and nuclear LAZY1 lower in brxl4 mutants compared with the wild type. To explain these results, we suggest that BRXL4 reduces the amount of LAZY1 at the plasma membrane where it functions in gravity signaling and promotes LAZY1 accumulation in the nucleus where it reduces LAZY1 expression, possibly by suppressing its own transcription. This explanation of how BRXL4 negatively regulates LAZY1 suggests ways to modify shoot system architecture for practical purposes. John Wiley and Sons Inc. 2022-12-24 2023-01 /pmc/articles/PMC10107345/ /pubmed/36478485 http://dx.doi.org/10.1111/tpj.16055 Text en © 2022 The Authors. The Plant Journal published by Society for Experimental Biology and John Wiley & Sons Ltd. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Original Articles
Che, Ximing
Splitt, Bessie L.
Eckholm, Magnus T.
Miller, Nathan D.
Spalding, Edgar P.
BRXL4‐LAZY1 interaction at the plasma membrane controls Arabidopsis branch angle and gravitropism
title BRXL4‐LAZY1 interaction at the plasma membrane controls Arabidopsis branch angle and gravitropism
title_full BRXL4‐LAZY1 interaction at the plasma membrane controls Arabidopsis branch angle and gravitropism
title_fullStr BRXL4‐LAZY1 interaction at the plasma membrane controls Arabidopsis branch angle and gravitropism
title_full_unstemmed BRXL4‐LAZY1 interaction at the plasma membrane controls Arabidopsis branch angle and gravitropism
title_short BRXL4‐LAZY1 interaction at the plasma membrane controls Arabidopsis branch angle and gravitropism
title_sort brxl4‐lazy1 interaction at the plasma membrane controls arabidopsis branch angle and gravitropism
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10107345/
https://www.ncbi.nlm.nih.gov/pubmed/36478485
http://dx.doi.org/10.1111/tpj.16055
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