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Loss of ZNF32 augments the regeneration of nervous lateral line system through negative regulation of SOX2 transcription

Human zinc finger protein 32 (ZNF32) is a Cys2-His2 zinc-finger transcription factor that plays an important role in cell fate, yet much of its function remains unknown. Here, we reveal that the zebrafish ZNF32 homologue zfZNF32 is expressed in the nervous system, particularly in the lateral line sy...

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Autores principales: Wei, Yuyan, Li, Kai, Yao, Shaohua, Gao, Junping, Li, Jun, Shang, Yanna, Zhang, Jie, Zhang, Le, Li, Yanyan, Mo, Xianming, Meng, Wentong, Xiang, Rong, Hu, Jiankun, Lin, Ping, Wei, Yuquan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5342562/
https://www.ncbi.nlm.nih.gov/pubmed/27626680
http://dx.doi.org/10.18632/oncotarget.11895
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author Wei, Yuyan
Li, Kai
Yao, Shaohua
Gao, Junping
Li, Jun
Shang, Yanna
Zhang, Jie
Zhang, Le
Li, Yanyan
Mo, Xianming
Meng, Wentong
Xiang, Rong
Hu, Jiankun
Lin, Ping
Wei, Yuquan
author_facet Wei, Yuyan
Li, Kai
Yao, Shaohua
Gao, Junping
Li, Jun
Shang, Yanna
Zhang, Jie
Zhang, Le
Li, Yanyan
Mo, Xianming
Meng, Wentong
Xiang, Rong
Hu, Jiankun
Lin, Ping
Wei, Yuquan
author_sort Wei, Yuyan
collection PubMed
description Human zinc finger protein 32 (ZNF32) is a Cys2-His2 zinc-finger transcription factor that plays an important role in cell fate, yet much of its function remains unknown. Here, we reveal that the zebrafish ZNF32 homologue zfZNF32 is expressed in the nervous system, particularly in the lateral line system. ZfZNF32 knock-out zebrafish (zfZNF(−/−)) were generated using the CRISPR-associated protein 9 system. We found that the regenerative capacity of the lateral line system was increased in zfZNF(−/−) upon hair cell damage compared with the wild type. Moreover, SOX2 was essential for the zfZNF32-dependent modulation of lateral line system regeneration. Mechanistic studies showed that ZNF32 suppressed SOX2 transcription by directly binding to a consensus sequence (5′-gcattt-32) in the SOX2 promoter. In addition, ZNF32 localizes to the nucleus, and we have identified that amino acids 1-169 (Aa 1-169) and each of three independent nuclear localization signals (NLSs) in ZNF32 are indispensable for ZNF32 nuclear trafficking. Mutating the NLSs disrupted the inhibitory effect of ZNF32 in SOX2 expression, highlighting the critical role of the NLSs in ZNF32 function. Our findings reveal a pivotal role for ZNF32 function in SOX2 expression and regeneration regulation.
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spelling pubmed-53425622017-03-24 Loss of ZNF32 augments the regeneration of nervous lateral line system through negative regulation of SOX2 transcription Wei, Yuyan Li, Kai Yao, Shaohua Gao, Junping Li, Jun Shang, Yanna Zhang, Jie Zhang, Le Li, Yanyan Mo, Xianming Meng, Wentong Xiang, Rong Hu, Jiankun Lin, Ping Wei, Yuquan Oncotarget Research Paper Human zinc finger protein 32 (ZNF32) is a Cys2-His2 zinc-finger transcription factor that plays an important role in cell fate, yet much of its function remains unknown. Here, we reveal that the zebrafish ZNF32 homologue zfZNF32 is expressed in the nervous system, particularly in the lateral line system. ZfZNF32 knock-out zebrafish (zfZNF(−/−)) were generated using the CRISPR-associated protein 9 system. We found that the regenerative capacity of the lateral line system was increased in zfZNF(−/−) upon hair cell damage compared with the wild type. Moreover, SOX2 was essential for the zfZNF32-dependent modulation of lateral line system regeneration. Mechanistic studies showed that ZNF32 suppressed SOX2 transcription by directly binding to a consensus sequence (5′-gcattt-32) in the SOX2 promoter. In addition, ZNF32 localizes to the nucleus, and we have identified that amino acids 1-169 (Aa 1-169) and each of three independent nuclear localization signals (NLSs) in ZNF32 are indispensable for ZNF32 nuclear trafficking. Mutating the NLSs disrupted the inhibitory effect of ZNF32 in SOX2 expression, highlighting the critical role of the NLSs in ZNF32 function. Our findings reveal a pivotal role for ZNF32 function in SOX2 expression and regeneration regulation. Impact Journals LLC 2016-09-08 /pmc/articles/PMC5342562/ /pubmed/27626680 http://dx.doi.org/10.18632/oncotarget.11895 Text en Copyright: © 2016 Wei et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Paper
Wei, Yuyan
Li, Kai
Yao, Shaohua
Gao, Junping
Li, Jun
Shang, Yanna
Zhang, Jie
Zhang, Le
Li, Yanyan
Mo, Xianming
Meng, Wentong
Xiang, Rong
Hu, Jiankun
Lin, Ping
Wei, Yuquan
Loss of ZNF32 augments the regeneration of nervous lateral line system through negative regulation of SOX2 transcription
title Loss of ZNF32 augments the regeneration of nervous lateral line system through negative regulation of SOX2 transcription
title_full Loss of ZNF32 augments the regeneration of nervous lateral line system through negative regulation of SOX2 transcription
title_fullStr Loss of ZNF32 augments the regeneration of nervous lateral line system through negative regulation of SOX2 transcription
title_full_unstemmed Loss of ZNF32 augments the regeneration of nervous lateral line system through negative regulation of SOX2 transcription
title_short Loss of ZNF32 augments the regeneration of nervous lateral line system through negative regulation of SOX2 transcription
title_sort loss of znf32 augments the regeneration of nervous lateral line system through negative regulation of sox2 transcription
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5342562/
https://www.ncbi.nlm.nih.gov/pubmed/27626680
http://dx.doi.org/10.18632/oncotarget.11895
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