The biogenesis of CLEL peptides involves several processing events in consecutive compartments of the secretory pathway

Post-translationally modified peptides are involved in many aspects of plant growth and development. The maturation of these peptides from their larger precursors is still poorly understood. We show here that the biogenesis of CLEL6 and CLEL9 peptides in Arabidopsis thaliana requires a series of pro...
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Autor*in:	Nils Stührwohldt [verfasserIn] Stefan Scholl [verfasserIn] Lisa Lang [verfasserIn] Julia Katzenberger [verfasserIn] Karin Schumacher [verfasserIn] Andreas Schaller [verfasserIn]

Format:	E-Artikel
Sprache:	Englisch

Erschienen:	2020

Schlagwörter:	post-translational modification precursor processing peptide hormone subtilase subtilisin-like proteinase peptide signaling

Übergeordnetes Werk:	In: eLife - eLife Sciences Publications Ltd, 2013, 9(2020)
Übergeordnetes Werk:	volume:9 ; year:2020

Links:	Link aufrufen Link aufrufen Link aufrufen Journal toc

DOI / URN:	10.7554/eLife.55580

Katalog-ID:	DOAJ022147756

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allfields	10.7554/eLife.55580 doi (DE-627)DOAJ022147756 (DE-599)DOAJb6351ed29cb74dd98fb395304e16188a DE-627 ger DE-627 rakwb eng QH301-705.5 Nils Stührwohldt verfasserin aut The biogenesis of CLEL peptides involves several processing events in consecutive compartments of the secretory pathway 2020 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Post-translationally modified peptides are involved in many aspects of plant growth and development. The maturation of these peptides from their larger precursors is still poorly understood. We show here that the biogenesis of CLEL6 and CLEL9 peptides in Arabidopsis thaliana requires a series of processing events in consecutive compartments of the secretory pathway. Following cleavage of the signal peptide upon entry into the endoplasmic reticulum (ER), the peptide precursors are processed in the cis-Golgi by the subtilase SBT6.1. SBT6.1-mediated cleavage within the variable domain allows for continued passage of the partially processed precursors through the secretory pathway, and for subsequent post-translational modifications including tyrosine sulfation and proline hydroxylation within, and proteolytic maturation after exit from the Golgi. Activation by subtilases including SBT3.8 in post-Golgi compartments depends on the N-terminal aspartate of the mature peptides. Our work highlights the complexity of post-translational precursor maturation allowing for stringent control of peptide biogenesis. post-translational modification precursor processing peptide hormone subtilase subtilisin-like proteinase peptide signaling Medicine R Science Q Biology (General) Stefan Scholl verfasserin aut Lisa Lang verfasserin aut Julia Katzenberger verfasserin aut Karin Schumacher verfasserin aut Andreas Schaller verfasserin aut In eLife eLife Sciences Publications Ltd, 2013 9(2020) (DE-627)728518384 (DE-600)2687154-3 2050084X nnns volume:9 year:2020 https://doi.org/10.7554/eLife.55580 kostenfrei https://doaj.org/article/b6351ed29cb74dd98fb395304e16188a kostenfrei https://elifesciences.org/articles/55580 kostenfrei https://doaj.org/toc/2050-084X Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_2003 GBV_ILN_2014 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4335 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 9 2020
spelling	10.7554/eLife.55580 doi (DE-627)DOAJ022147756 (DE-599)DOAJb6351ed29cb74dd98fb395304e16188a DE-627 ger DE-627 rakwb eng QH301-705.5 Nils Stührwohldt verfasserin aut The biogenesis of CLEL peptides involves several processing events in consecutive compartments of the secretory pathway 2020 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Post-translationally modified peptides are involved in many aspects of plant growth and development. The maturation of these peptides from their larger precursors is still poorly understood. We show here that the biogenesis of CLEL6 and CLEL9 peptides in Arabidopsis thaliana requires a series of processing events in consecutive compartments of the secretory pathway. Following cleavage of the signal peptide upon entry into the endoplasmic reticulum (ER), the peptide precursors are processed in the cis-Golgi by the subtilase SBT6.1. SBT6.1-mediated cleavage within the variable domain allows for continued passage of the partially processed precursors through the secretory pathway, and for subsequent post-translational modifications including tyrosine sulfation and proline hydroxylation within, and proteolytic maturation after exit from the Golgi. Activation by subtilases including SBT3.8 in post-Golgi compartments depends on the N-terminal aspartate of the mature peptides. Our work highlights the complexity of post-translational precursor maturation allowing for stringent control of peptide biogenesis. post-translational modification precursor processing peptide hormone subtilase subtilisin-like proteinase peptide signaling Medicine R Science Q Biology (General) Stefan Scholl verfasserin aut Lisa Lang verfasserin aut Julia Katzenberger verfasserin aut Karin Schumacher verfasserin aut Andreas Schaller verfasserin aut In eLife eLife Sciences Publications Ltd, 2013 9(2020) (DE-627)728518384 (DE-600)2687154-3 2050084X nnns volume:9 year:2020 https://doi.org/10.7554/eLife.55580 kostenfrei https://doaj.org/article/b6351ed29cb74dd98fb395304e16188a kostenfrei https://elifesciences.org/articles/55580 kostenfrei https://doaj.org/toc/2050-084X Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_2003 GBV_ILN_2014 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4335 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 9 2020
allfields_unstemmed	10.7554/eLife.55580 doi (DE-627)DOAJ022147756 (DE-599)DOAJb6351ed29cb74dd98fb395304e16188a DE-627 ger DE-627 rakwb eng QH301-705.5 Nils Stührwohldt verfasserin aut The biogenesis of CLEL peptides involves several processing events in consecutive compartments of the secretory pathway 2020 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Post-translationally modified peptides are involved in many aspects of plant growth and development. The maturation of these peptides from their larger precursors is still poorly understood. We show here that the biogenesis of CLEL6 and CLEL9 peptides in Arabidopsis thaliana requires a series of processing events in consecutive compartments of the secretory pathway. Following cleavage of the signal peptide upon entry into the endoplasmic reticulum (ER), the peptide precursors are processed in the cis-Golgi by the subtilase SBT6.1. SBT6.1-mediated cleavage within the variable domain allows for continued passage of the partially processed precursors through the secretory pathway, and for subsequent post-translational modifications including tyrosine sulfation and proline hydroxylation within, and proteolytic maturation after exit from the Golgi. Activation by subtilases including SBT3.8 in post-Golgi compartments depends on the N-terminal aspartate of the mature peptides. Our work highlights the complexity of post-translational precursor maturation allowing for stringent control of peptide biogenesis. post-translational modification precursor processing peptide hormone subtilase subtilisin-like proteinase peptide signaling Medicine R Science Q Biology (General) Stefan Scholl verfasserin aut Lisa Lang verfasserin aut Julia Katzenberger verfasserin aut Karin Schumacher verfasserin aut Andreas Schaller verfasserin aut In eLife eLife Sciences Publications Ltd, 2013 9(2020) (DE-627)728518384 (DE-600)2687154-3 2050084X nnns volume:9 year:2020 https://doi.org/10.7554/eLife.55580 kostenfrei https://doaj.org/article/b6351ed29cb74dd98fb395304e16188a kostenfrei https://elifesciences.org/articles/55580 kostenfrei https://doaj.org/toc/2050-084X Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_2003 GBV_ILN_2014 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4335 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 9 2020
allfieldsGer	10.7554/eLife.55580 doi (DE-627)DOAJ022147756 (DE-599)DOAJb6351ed29cb74dd98fb395304e16188a DE-627 ger DE-627 rakwb eng QH301-705.5 Nils Stührwohldt verfasserin aut The biogenesis of CLEL peptides involves several processing events in consecutive compartments of the secretory pathway 2020 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Post-translationally modified peptides are involved in many aspects of plant growth and development. The maturation of these peptides from their larger precursors is still poorly understood. We show here that the biogenesis of CLEL6 and CLEL9 peptides in Arabidopsis thaliana requires a series of processing events in consecutive compartments of the secretory pathway. Following cleavage of the signal peptide upon entry into the endoplasmic reticulum (ER), the peptide precursors are processed in the cis-Golgi by the subtilase SBT6.1. SBT6.1-mediated cleavage within the variable domain allows for continued passage of the partially processed precursors through the secretory pathway, and for subsequent post-translational modifications including tyrosine sulfation and proline hydroxylation within, and proteolytic maturation after exit from the Golgi. Activation by subtilases including SBT3.8 in post-Golgi compartments depends on the N-terminal aspartate of the mature peptides. Our work highlights the complexity of post-translational precursor maturation allowing for stringent control of peptide biogenesis. post-translational modification precursor processing peptide hormone subtilase subtilisin-like proteinase peptide signaling Medicine R Science Q Biology (General) Stefan Scholl verfasserin aut Lisa Lang verfasserin aut Julia Katzenberger verfasserin aut Karin Schumacher verfasserin aut Andreas Schaller verfasserin aut In eLife eLife Sciences Publications Ltd, 2013 9(2020) (DE-627)728518384 (DE-600)2687154-3 2050084X nnns volume:9 year:2020 https://doi.org/10.7554/eLife.55580 kostenfrei https://doaj.org/article/b6351ed29cb74dd98fb395304e16188a kostenfrei https://elifesciences.org/articles/55580 kostenfrei https://doaj.org/toc/2050-084X Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_2003 GBV_ILN_2014 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4335 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 9 2020
allfieldsSound	10.7554/eLife.55580 doi (DE-627)DOAJ022147756 (DE-599)DOAJb6351ed29cb74dd98fb395304e16188a DE-627 ger DE-627 rakwb eng QH301-705.5 Nils Stührwohldt verfasserin aut The biogenesis of CLEL peptides involves several processing events in consecutive compartments of the secretory pathway 2020 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Post-translationally modified peptides are involved in many aspects of plant growth and development. The maturation of these peptides from their larger precursors is still poorly understood. We show here that the biogenesis of CLEL6 and CLEL9 peptides in Arabidopsis thaliana requires a series of processing events in consecutive compartments of the secretory pathway. Following cleavage of the signal peptide upon entry into the endoplasmic reticulum (ER), the peptide precursors are processed in the cis-Golgi by the subtilase SBT6.1. SBT6.1-mediated cleavage within the variable domain allows for continued passage of the partially processed precursors through the secretory pathway, and for subsequent post-translational modifications including tyrosine sulfation and proline hydroxylation within, and proteolytic maturation after exit from the Golgi. Activation by subtilases including SBT3.8 in post-Golgi compartments depends on the N-terminal aspartate of the mature peptides. Our work highlights the complexity of post-translational precursor maturation allowing for stringent control of peptide biogenesis. post-translational modification precursor processing peptide hormone subtilase subtilisin-like proteinase peptide signaling Medicine R Science Q Biology (General) Stefan Scholl verfasserin aut Lisa Lang verfasserin aut Julia Katzenberger verfasserin aut Karin Schumacher verfasserin aut Andreas Schaller verfasserin aut In eLife eLife Sciences Publications Ltd, 2013 9(2020) (DE-627)728518384 (DE-600)2687154-3 2050084X nnns volume:9 year:2020 https://doi.org/10.7554/eLife.55580 kostenfrei https://doaj.org/article/b6351ed29cb74dd98fb395304e16188a kostenfrei https://elifesciences.org/articles/55580 kostenfrei https://doaj.org/toc/2050-084X Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_2003 GBV_ILN_2014 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4335 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 9 2020
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container_title	eLife
authorswithroles_txt_mv	Nils Stührwohldt @@aut@@ Stefan Scholl @@aut@@ Lisa Lang @@aut@@ Julia Katzenberger @@aut@@ Karin Schumacher @@aut@@ Andreas Schaller @@aut@@
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author	Nils Stührwohldt
spellingShingle	Nils Stührwohldt misc QH301-705.5 misc post-translational modification misc precursor processing misc peptide hormone misc subtilase misc subtilisin-like proteinase misc peptide signaling misc Medicine misc R misc Science misc Q misc Biology (General) The biogenesis of CLEL peptides involves several processing events in consecutive compartments of the secretory pathway
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topic_title	QH301-705.5 The biogenesis of CLEL peptides involves several processing events in consecutive compartments of the secretory pathway post-translational modification precursor processing peptide hormone subtilase subtilisin-like proteinase peptide signaling
topic	misc QH301-705.5 misc post-translational modification misc precursor processing misc peptide hormone misc subtilase misc subtilisin-like proteinase misc peptide signaling misc Medicine misc R misc Science misc Q misc Biology (General)
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title	The biogenesis of CLEL peptides involves several processing events in consecutive compartments of the secretory pathway
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title_full	The biogenesis of CLEL peptides involves several processing events in consecutive compartments of the secretory pathway
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title_sort	biogenesis of clel peptides involves several processing events in consecutive compartments of the secretory pathway
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title_auth	The biogenesis of CLEL peptides involves several processing events in consecutive compartments of the secretory pathway
abstract	Post-translationally modified peptides are involved in many aspects of plant growth and development. The maturation of these peptides from their larger precursors is still poorly understood. We show here that the biogenesis of CLEL6 and CLEL9 peptides in Arabidopsis thaliana requires a series of processing events in consecutive compartments of the secretory pathway. Following cleavage of the signal peptide upon entry into the endoplasmic reticulum (ER), the peptide precursors are processed in the cis-Golgi by the subtilase SBT6.1. SBT6.1-mediated cleavage within the variable domain allows for continued passage of the partially processed precursors through the secretory pathway, and for subsequent post-translational modifications including tyrosine sulfation and proline hydroxylation within, and proteolytic maturation after exit from the Golgi. Activation by subtilases including SBT3.8 in post-Golgi compartments depends on the N-terminal aspartate of the mature peptides. Our work highlights the complexity of post-translational precursor maturation allowing for stringent control of peptide biogenesis.
abstractGer	Post-translationally modified peptides are involved in many aspects of plant growth and development. The maturation of these peptides from their larger precursors is still poorly understood. We show here that the biogenesis of CLEL6 and CLEL9 peptides in Arabidopsis thaliana requires a series of processing events in consecutive compartments of the secretory pathway. Following cleavage of the signal peptide upon entry into the endoplasmic reticulum (ER), the peptide precursors are processed in the cis-Golgi by the subtilase SBT6.1. SBT6.1-mediated cleavage within the variable domain allows for continued passage of the partially processed precursors through the secretory pathway, and for subsequent post-translational modifications including tyrosine sulfation and proline hydroxylation within, and proteolytic maturation after exit from the Golgi. Activation by subtilases including SBT3.8 in post-Golgi compartments depends on the N-terminal aspartate of the mature peptides. Our work highlights the complexity of post-translational precursor maturation allowing for stringent control of peptide biogenesis.
abstract_unstemmed	Post-translationally modified peptides are involved in many aspects of plant growth and development. The maturation of these peptides from their larger precursors is still poorly understood. We show here that the biogenesis of CLEL6 and CLEL9 peptides in Arabidopsis thaliana requires a series of processing events in consecutive compartments of the secretory pathway. Following cleavage of the signal peptide upon entry into the endoplasmic reticulum (ER), the peptide precursors are processed in the cis-Golgi by the subtilase SBT6.1. SBT6.1-mediated cleavage within the variable domain allows for continued passage of the partially processed precursors through the secretory pathway, and for subsequent post-translational modifications including tyrosine sulfation and proline hydroxylation within, and proteolytic maturation after exit from the Golgi. Activation by subtilases including SBT3.8 in post-Golgi compartments depends on the N-terminal aspartate of the mature peptides. Our work highlights the complexity of post-translational precursor maturation allowing for stringent control of peptide biogenesis.
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title_short	The biogenesis of CLEL peptides involves several processing events in consecutive compartments of the secretory pathway
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The biogenesis of CLEL peptides involves several processing events in consecutive compartments of the secretory pathway

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