Cargando…
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...
Autores principales: | , , , , , , , , , , , , , , |
---|---|
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 |
_version_ | 1782513209191694336 |
---|---|
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. |
format | Online Article Text |
id | pubmed-5342562 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT weiyuyan lossofznf32augmentstheregenerationofnervouslaterallinesystemthroughnegativeregulationofsox2transcription AT likai lossofznf32augmentstheregenerationofnervouslaterallinesystemthroughnegativeregulationofsox2transcription AT yaoshaohua lossofznf32augmentstheregenerationofnervouslaterallinesystemthroughnegativeregulationofsox2transcription AT gaojunping lossofznf32augmentstheregenerationofnervouslaterallinesystemthroughnegativeregulationofsox2transcription AT lijun lossofznf32augmentstheregenerationofnervouslaterallinesystemthroughnegativeregulationofsox2transcription AT shangyanna lossofznf32augmentstheregenerationofnervouslaterallinesystemthroughnegativeregulationofsox2transcription AT zhangjie lossofznf32augmentstheregenerationofnervouslaterallinesystemthroughnegativeregulationofsox2transcription AT zhangle lossofznf32augmentstheregenerationofnervouslaterallinesystemthroughnegativeregulationofsox2transcription AT liyanyan lossofznf32augmentstheregenerationofnervouslaterallinesystemthroughnegativeregulationofsox2transcription AT moxianming lossofznf32augmentstheregenerationofnervouslaterallinesystemthroughnegativeregulationofsox2transcription AT mengwentong lossofznf32augmentstheregenerationofnervouslaterallinesystemthroughnegativeregulationofsox2transcription AT xiangrong lossofznf32augmentstheregenerationofnervouslaterallinesystemthroughnegativeregulationofsox2transcription AT hujiankun lossofznf32augmentstheregenerationofnervouslaterallinesystemthroughnegativeregulationofsox2transcription AT linping lossofznf32augmentstheregenerationofnervouslaterallinesystemthroughnegativeregulationofsox2transcription AT weiyuquan lossofznf32augmentstheregenerationofnervouslaterallinesystemthroughnegativeregulationofsox2transcription |