Cargando…
Gawky modulates MTF-1-mediated transcription activation and metal discrimination
Metal-induced genes are usually transcribed at relatively low levels under normal conditions and are rapidly activated by heavy metal stress. Many of these genes respond preferentially to specific metal-stressed conditions. However, the mechanism by which the general transcription machinery discrimi...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8216474/ https://www.ncbi.nlm.nih.gov/pubmed/34107019 http://dx.doi.org/10.1093/nar/gkab474 |
_version_ | 1783710426376175616 |
---|---|
author | Jia, Ruirui Song, Zhenxing Lin, Jiamei Li, Zhengguo Shan, Ge Huang, Chuan |
author_facet | Jia, Ruirui Song, Zhenxing Lin, Jiamei Li, Zhengguo Shan, Ge Huang, Chuan |
author_sort | Jia, Ruirui |
collection | PubMed |
description | Metal-induced genes are usually transcribed at relatively low levels under normal conditions and are rapidly activated by heavy metal stress. Many of these genes respond preferentially to specific metal-stressed conditions. However, the mechanism by which the general transcription machinery discriminates metal stress from normal conditions and the regulation of MTF-1-meditated metal discrimination are poorly characterized. Using a focused RNAi screening in Drosophila Schneider 2 (S2) cells, we identified a novel activator, the Drosophila gawky, of metal-responsive genes. Depletion of gawky has almost no effect on the basal transcription of the metallothionein (MT) genes, but impairs the metal-induced transcription by inducing the dissociation of MTF-1 from the MT promoters and the deficient nuclear import of MTF-1 under metal-stressed conditions. This suggests that gawky serves as a ‘checkpoint’ for metal stress and metal-induced transcription. In fact, regular mRNAs are converted into gawky-controlled transcripts if expressed under the control of a metal-responsive promoter, suggesting that whether transcription undergoes gawky-mediated regulation is encrypted therein. Additionally, lack of gawky eliminates the DNA binding bias of MTF-1 and the transcription preference of metal-specific genes. This suggests a combinatorial control of metal discrimination by gawky, MTF-1, and MTF-1 binding sites. |
format | Online Article Text |
id | pubmed-8216474 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-82164742021-06-22 Gawky modulates MTF-1-mediated transcription activation and metal discrimination Jia, Ruirui Song, Zhenxing Lin, Jiamei Li, Zhengguo Shan, Ge Huang, Chuan Nucleic Acids Res Gene regulation, Chromatin and Epigenetics Metal-induced genes are usually transcribed at relatively low levels under normal conditions and are rapidly activated by heavy metal stress. Many of these genes respond preferentially to specific metal-stressed conditions. However, the mechanism by which the general transcription machinery discriminates metal stress from normal conditions and the regulation of MTF-1-meditated metal discrimination are poorly characterized. Using a focused RNAi screening in Drosophila Schneider 2 (S2) cells, we identified a novel activator, the Drosophila gawky, of metal-responsive genes. Depletion of gawky has almost no effect on the basal transcription of the metallothionein (MT) genes, but impairs the metal-induced transcription by inducing the dissociation of MTF-1 from the MT promoters and the deficient nuclear import of MTF-1 under metal-stressed conditions. This suggests that gawky serves as a ‘checkpoint’ for metal stress and metal-induced transcription. In fact, regular mRNAs are converted into gawky-controlled transcripts if expressed under the control of a metal-responsive promoter, suggesting that whether transcription undergoes gawky-mediated regulation is encrypted therein. Additionally, lack of gawky eliminates the DNA binding bias of MTF-1 and the transcription preference of metal-specific genes. This suggests a combinatorial control of metal discrimination by gawky, MTF-1, and MTF-1 binding sites. Oxford University Press 2021-06-09 /pmc/articles/PMC8216474/ /pubmed/34107019 http://dx.doi.org/10.1093/nar/gkab474 Text en © The Author(s) 2021. Published by Oxford University Press on behalf of Nucleic Acids Research. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Gene regulation, Chromatin and Epigenetics Jia, Ruirui Song, Zhenxing Lin, Jiamei Li, Zhengguo Shan, Ge Huang, Chuan Gawky modulates MTF-1-mediated transcription activation and metal discrimination |
title | Gawky modulates MTF-1-mediated transcription activation and metal discrimination |
title_full | Gawky modulates MTF-1-mediated transcription activation and metal discrimination |
title_fullStr | Gawky modulates MTF-1-mediated transcription activation and metal discrimination |
title_full_unstemmed | Gawky modulates MTF-1-mediated transcription activation and metal discrimination |
title_short | Gawky modulates MTF-1-mediated transcription activation and metal discrimination |
title_sort | gawky modulates mtf-1-mediated transcription activation and metal discrimination |
topic | Gene regulation, Chromatin and Epigenetics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8216474/ https://www.ncbi.nlm.nih.gov/pubmed/34107019 http://dx.doi.org/10.1093/nar/gkab474 |
work_keys_str_mv | AT jiaruirui gawkymodulatesmtf1mediatedtranscriptionactivationandmetaldiscrimination AT songzhenxing gawkymodulatesmtf1mediatedtranscriptionactivationandmetaldiscrimination AT linjiamei gawkymodulatesmtf1mediatedtranscriptionactivationandmetaldiscrimination AT lizhengguo gawkymodulatesmtf1mediatedtranscriptionactivationandmetaldiscrimination AT shange gawkymodulatesmtf1mediatedtranscriptionactivationandmetaldiscrimination AT huangchuan gawkymodulatesmtf1mediatedtranscriptionactivationandmetaldiscrimination |