Cargando…

Aspartic proteases modulate programmed cell death and secondary cell wall synthesis during wood formation in poplar

Programmed cell death (PCD) is essential for wood development in trees. However, the determination of crucial factors involved in xylem PCD of wood development is still lacking. Here, two Populus trichocarpa typical aspartic protease (AP) genes, AP17 and AP45, modulate xylem maturation, especially f...

Descripción completa

Detalles Bibliográficos
Autores principales: Cao, Shenquan, Guo, Mengjie, Cheng, Jiyao, Cheng, Hao, Liu, Xiaomeng, Ji, Huanhuan, Liu, Guanjun, Cheng, Yuxiang, Yang, Chuanping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9629783/
https://www.ncbi.nlm.nih.gov/pubmed/36040843
http://dx.doi.org/10.1093/jxb/erac347
_version_ 1784823466963238912
author Cao, Shenquan
Guo, Mengjie
Cheng, Jiyao
Cheng, Hao
Liu, Xiaomeng
Ji, Huanhuan
Liu, Guanjun
Cheng, Yuxiang
Yang, Chuanping
author_facet Cao, Shenquan
Guo, Mengjie
Cheng, Jiyao
Cheng, Hao
Liu, Xiaomeng
Ji, Huanhuan
Liu, Guanjun
Cheng, Yuxiang
Yang, Chuanping
author_sort Cao, Shenquan
collection PubMed
description Programmed cell death (PCD) is essential for wood development in trees. However, the determination of crucial factors involved in xylem PCD of wood development is still lacking. Here, two Populus trichocarpa typical aspartic protease (AP) genes, AP17 and AP45, modulate xylem maturation, especially fibre PCD, during wood formation. AP17 and AP45 were dominantly expressed in the fibres of secondary xylem, as suggested by GUS expression in APpro::GUS transgenic plants. Cas9/gRNA-induced AP17 or AP45 mutants delayed secondary xylem fibre PCD, and ap17ap45 double mutants showed more serious defects. Conversely, AP17 overexpression caused premature PCD in secondary xylem fibres, indicating a positive modulation in wood fibre PCD. Loss of AP17 and AP45 did not alter wood fibre wall thickness, whereas the ap17ap45 mutants showed a low lignin content in wood. However, AP17 overexpression led to a significant decrease in wood fibre wall thickness and lignin content, revealing the involvement in secondary cell wall synthesis during wood formation. In addition, the ap17ap45 mutant and AP17 overexpression plants resulted in a significant increase in saccharification yield in wood. Overall, AP17 and AP45 are crucial modulators in xylem maturation during wood development, providing potential candidate genes for engineering lignocellulosic wood for biofuel utilization.
format Online
Article
Text
id pubmed-9629783
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Oxford University Press
record_format MEDLINE/PubMed
spelling pubmed-96297832022-11-04 Aspartic proteases modulate programmed cell death and secondary cell wall synthesis during wood formation in poplar Cao, Shenquan Guo, Mengjie Cheng, Jiyao Cheng, Hao Liu, Xiaomeng Ji, Huanhuan Liu, Guanjun Cheng, Yuxiang Yang, Chuanping J Exp Bot Research Papers Programmed cell death (PCD) is essential for wood development in trees. However, the determination of crucial factors involved in xylem PCD of wood development is still lacking. Here, two Populus trichocarpa typical aspartic protease (AP) genes, AP17 and AP45, modulate xylem maturation, especially fibre PCD, during wood formation. AP17 and AP45 were dominantly expressed in the fibres of secondary xylem, as suggested by GUS expression in APpro::GUS transgenic plants. Cas9/gRNA-induced AP17 or AP45 mutants delayed secondary xylem fibre PCD, and ap17ap45 double mutants showed more serious defects. Conversely, AP17 overexpression caused premature PCD in secondary xylem fibres, indicating a positive modulation in wood fibre PCD. Loss of AP17 and AP45 did not alter wood fibre wall thickness, whereas the ap17ap45 mutants showed a low lignin content in wood. However, AP17 overexpression led to a significant decrease in wood fibre wall thickness and lignin content, revealing the involvement in secondary cell wall synthesis during wood formation. In addition, the ap17ap45 mutant and AP17 overexpression plants resulted in a significant increase in saccharification yield in wood. Overall, AP17 and AP45 are crucial modulators in xylem maturation during wood development, providing potential candidate genes for engineering lignocellulosic wood for biofuel utilization. Oxford University Press 2022-08-30 /pmc/articles/PMC9629783/ /pubmed/36040843 http://dx.doi.org/10.1093/jxb/erac347 Text en © The Author(s) 2022. Published by Oxford University Press on behalf of the Society for Experimental Biology. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Papers
Cao, Shenquan
Guo, Mengjie
Cheng, Jiyao
Cheng, Hao
Liu, Xiaomeng
Ji, Huanhuan
Liu, Guanjun
Cheng, Yuxiang
Yang, Chuanping
Aspartic proteases modulate programmed cell death and secondary cell wall synthesis during wood formation in poplar
title Aspartic proteases modulate programmed cell death and secondary cell wall synthesis during wood formation in poplar
title_full Aspartic proteases modulate programmed cell death and secondary cell wall synthesis during wood formation in poplar
title_fullStr Aspartic proteases modulate programmed cell death and secondary cell wall synthesis during wood formation in poplar
title_full_unstemmed Aspartic proteases modulate programmed cell death and secondary cell wall synthesis during wood formation in poplar
title_short Aspartic proteases modulate programmed cell death and secondary cell wall synthesis during wood formation in poplar
title_sort aspartic proteases modulate programmed cell death and secondary cell wall synthesis during wood formation in poplar
topic Research Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9629783/
https://www.ncbi.nlm.nih.gov/pubmed/36040843
http://dx.doi.org/10.1093/jxb/erac347
work_keys_str_mv AT caoshenquan asparticproteasesmodulateprogrammedcelldeathandsecondarycellwallsynthesisduringwoodformationinpoplar
AT guomengjie asparticproteasesmodulateprogrammedcelldeathandsecondarycellwallsynthesisduringwoodformationinpoplar
AT chengjiyao asparticproteasesmodulateprogrammedcelldeathandsecondarycellwallsynthesisduringwoodformationinpoplar
AT chenghao asparticproteasesmodulateprogrammedcelldeathandsecondarycellwallsynthesisduringwoodformationinpoplar
AT liuxiaomeng asparticproteasesmodulateprogrammedcelldeathandsecondarycellwallsynthesisduringwoodformationinpoplar
AT jihuanhuan asparticproteasesmodulateprogrammedcelldeathandsecondarycellwallsynthesisduringwoodformationinpoplar
AT liuguanjun asparticproteasesmodulateprogrammedcelldeathandsecondarycellwallsynthesisduringwoodformationinpoplar
AT chengyuxiang asparticproteasesmodulateprogrammedcelldeathandsecondarycellwallsynthesisduringwoodformationinpoplar
AT yangchuanping asparticproteasesmodulateprogrammedcelldeathandsecondarycellwallsynthesisduringwoodformationinpoplar