Cargando…

GhL1L1 affects cell fate specification by regulating GhPIN1‐mediated auxin distribution

Auxin is as an efficient initiator and regulator of cell fate during somatic embryogenesis (SE), but the molecular mechanisms and regulating networks of this process are not well understood. In this report, we analysed SE process induced by Leafy cotyledon1‐like 1 (GhL1L1), a NF‐YB subfamily gene sp...

Descripción completa

Detalles Bibliográficos
Autores principales: Xu, Jiao, Yang, Xiyan, Li, Baoqi, Chen, Lin, Min, Ling, Zhang, Xianlong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6330550/
https://www.ncbi.nlm.nih.gov/pubmed/29754405
http://dx.doi.org/10.1111/pbi.12947
_version_ 1783387000142823424
author Xu, Jiao
Yang, Xiyan
Li, Baoqi
Chen, Lin
Min, Ling
Zhang, Xianlong
author_facet Xu, Jiao
Yang, Xiyan
Li, Baoqi
Chen, Lin
Min, Ling
Zhang, Xianlong
author_sort Xu, Jiao
collection PubMed
description Auxin is as an efficient initiator and regulator of cell fate during somatic embryogenesis (SE), but the molecular mechanisms and regulating networks of this process are not well understood. In this report, we analysed SE process induced by Leafy cotyledon1‐like 1 (GhL1L1), a NF‐YB subfamily gene specifically expressed in embryonic tissues in cotton. We also identified the target gene of GhL1L1, and its role in auxin distribution and cell fate specification during embryonic development was analysed. Overexpression of GhL1L1 accelerated embryonic cell formation, associated with an increased concentration of IAA in embryogenic calluses (ECs) and in the shoot apical meristem, corresponding to altered expression of the auxin transport gene GhPIN1. By contrast, GhL1L1‐deficient explants showed retarded embryonic cell formation, and the concentration of IAA was decreased in GhL1L1‐deficient ECs. Disruption of auxin distribution accelerated the specification of embryonic cell fate together with regulation of GhPIN1. Furthermore, we showed that PHOSPHATASE 2AA2 (GhPP2AA2) was activated by GhL1L1 through targeting the G‐box of its promoter, hence regulating the activity of GhPIN1 protein. Our results indicate that GhL1L1 functions as a key regulator in auxin distribution to regulate cell fate specification in cotton and contribute to the understanding of the complex process of SE in plant species.
format Online
Article
Text
id pubmed-6330550
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher John Wiley and Sons Inc.
record_format MEDLINE/PubMed
spelling pubmed-63305502019-01-17 GhL1L1 affects cell fate specification by regulating GhPIN1‐mediated auxin distribution Xu, Jiao Yang, Xiyan Li, Baoqi Chen, Lin Min, Ling Zhang, Xianlong Plant Biotechnol J Research Articles Auxin is as an efficient initiator and regulator of cell fate during somatic embryogenesis (SE), but the molecular mechanisms and regulating networks of this process are not well understood. In this report, we analysed SE process induced by Leafy cotyledon1‐like 1 (GhL1L1), a NF‐YB subfamily gene specifically expressed in embryonic tissues in cotton. We also identified the target gene of GhL1L1, and its role in auxin distribution and cell fate specification during embryonic development was analysed. Overexpression of GhL1L1 accelerated embryonic cell formation, associated with an increased concentration of IAA in embryogenic calluses (ECs) and in the shoot apical meristem, corresponding to altered expression of the auxin transport gene GhPIN1. By contrast, GhL1L1‐deficient explants showed retarded embryonic cell formation, and the concentration of IAA was decreased in GhL1L1‐deficient ECs. Disruption of auxin distribution accelerated the specification of embryonic cell fate together with regulation of GhPIN1. Furthermore, we showed that PHOSPHATASE 2AA2 (GhPP2AA2) was activated by GhL1L1 through targeting the G‐box of its promoter, hence regulating the activity of GhPIN1 protein. Our results indicate that GhL1L1 functions as a key regulator in auxin distribution to regulate cell fate specification in cotton and contribute to the understanding of the complex process of SE in plant species. John Wiley and Sons Inc. 2018-05-31 2019-01 /pmc/articles/PMC6330550/ /pubmed/29754405 http://dx.doi.org/10.1111/pbi.12947 Text en © 2018 The Authors. Plant Biotechnology Journal published by Society for Experimental Biology and The Association of Applied Biologists and John Wiley & Sons Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Xu, Jiao
Yang, Xiyan
Li, Baoqi
Chen, Lin
Min, Ling
Zhang, Xianlong
GhL1L1 affects cell fate specification by regulating GhPIN1‐mediated auxin distribution
title GhL1L1 affects cell fate specification by regulating GhPIN1‐mediated auxin distribution
title_full GhL1L1 affects cell fate specification by regulating GhPIN1‐mediated auxin distribution
title_fullStr GhL1L1 affects cell fate specification by regulating GhPIN1‐mediated auxin distribution
title_full_unstemmed GhL1L1 affects cell fate specification by regulating GhPIN1‐mediated auxin distribution
title_short GhL1L1 affects cell fate specification by regulating GhPIN1‐mediated auxin distribution
title_sort ghl1l1 affects cell fate specification by regulating ghpin1‐mediated auxin distribution
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6330550/
https://www.ncbi.nlm.nih.gov/pubmed/29754405
http://dx.doi.org/10.1111/pbi.12947
work_keys_str_mv AT xujiao ghl1l1affectscellfatespecificationbyregulatingghpin1mediatedauxindistribution
AT yangxiyan ghl1l1affectscellfatespecificationbyregulatingghpin1mediatedauxindistribution
AT libaoqi ghl1l1affectscellfatespecificationbyregulatingghpin1mediatedauxindistribution
AT chenlin ghl1l1affectscellfatespecificationbyregulatingghpin1mediatedauxindistribution
AT minling ghl1l1affectscellfatespecificationbyregulatingghpin1mediatedauxindistribution
AT zhangxianlong ghl1l1affectscellfatespecificationbyregulatingghpin1mediatedauxindistribution