Cargando…

Biochemical Analyses of Csx/Nkx2.5 Mutants and Their Structure–Function Relationship

A homeodomain-containing transcription factor Csx/Nkx2.5 is an important regulator of cardiogensis in mammals. There has been considerable interest in understanding determinants of the diverse cardiac phenotypes associated with Csx/Nkx2.5 mutations situated within or around the homeodomain in patien...

Descripción completa

Detalles Bibliográficos
Autores principales: Chen, Yun-Zi, Ying, Hua, Zhang, Jing, Cheng, Wei, Kang, Yuan-Xi, Hua, Zi-Chun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Molecular Diversity Preservation International (MDPI) 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3685383/
_version_ 1782273687010934784
author Chen, Yun-Zi
Ying, Hua
Zhang, Jing
Cheng, Wei
Kang, Yuan-Xi
Hua, Zi-Chun
author_facet Chen, Yun-Zi
Ying, Hua
Zhang, Jing
Cheng, Wei
Kang, Yuan-Xi
Hua, Zi-Chun
author_sort Chen, Yun-Zi
collection PubMed
description A homeodomain-containing transcription factor Csx/Nkx2.5 is an important regulator of cardiogensis in mammals. There has been considerable interest in understanding determinants of the diverse cardiac phenotypes associated with Csx/Nkx2.5 mutations situated within or around the homeodomain in patients. To make clear of the functional properties of the regions out of homeodomain, we found that mutants locate outside of the homeodomain retained intact nuclear localization and have nearly normal or increased transcriptional activity but impaired DNA binding capability, the C-terminus region exhibits an inhibitory function on transcriptional activity of wild type Csx/Nkx2.5, and the NK2-Specific Domain is likely to facilitate both DNA binding and protein-protein interaction. In the current study, deletion mutant in homeodomain displayed extremely different biological appearance from the mutants with deletion outside of the homeodomain, these may explain the clinical observation that patients with missense situated outside the homeodomain were not associated with atrioventricular conduction disturbance.
format Online
Article
Text
id pubmed-3685383
institution National Center for Biotechnology Information
language English
publishDate 2007
publisher Molecular Diversity Preservation International (MDPI)
record_format MEDLINE/PubMed
spelling pubmed-36853832013-06-19 Biochemical Analyses of Csx/Nkx2.5 Mutants and Their Structure–Function Relationship Chen, Yun-Zi Ying, Hua Zhang, Jing Cheng, Wei Kang, Yuan-Xi Hua, Zi-Chun Int J Mol Sci Full Research Paper A homeodomain-containing transcription factor Csx/Nkx2.5 is an important regulator of cardiogensis in mammals. There has been considerable interest in understanding determinants of the diverse cardiac phenotypes associated with Csx/Nkx2.5 mutations situated within or around the homeodomain in patients. To make clear of the functional properties of the regions out of homeodomain, we found that mutants locate outside of the homeodomain retained intact nuclear localization and have nearly normal or increased transcriptional activity but impaired DNA binding capability, the C-terminus region exhibits an inhibitory function on transcriptional activity of wild type Csx/Nkx2.5, and the NK2-Specific Domain is likely to facilitate both DNA binding and protein-protein interaction. In the current study, deletion mutant in homeodomain displayed extremely different biological appearance from the mutants with deletion outside of the homeodomain, these may explain the clinical observation that patients with missense situated outside the homeodomain were not associated with atrioventricular conduction disturbance. Molecular Diversity Preservation International (MDPI) 2007-04-12 /pmc/articles/PMC3685383/ Text en © 2007 by MDPI Reproduction is permitted for noncommercial purposes.
spellingShingle Full Research Paper
Chen, Yun-Zi
Ying, Hua
Zhang, Jing
Cheng, Wei
Kang, Yuan-Xi
Hua, Zi-Chun
Biochemical Analyses of Csx/Nkx2.5 Mutants and Their Structure–Function Relationship
title Biochemical Analyses of Csx/Nkx2.5 Mutants and Their Structure–Function Relationship
title_full Biochemical Analyses of Csx/Nkx2.5 Mutants and Their Structure–Function Relationship
title_fullStr Biochemical Analyses of Csx/Nkx2.5 Mutants and Their Structure–Function Relationship
title_full_unstemmed Biochemical Analyses of Csx/Nkx2.5 Mutants and Their Structure–Function Relationship
title_short Biochemical Analyses of Csx/Nkx2.5 Mutants and Their Structure–Function Relationship
title_sort biochemical analyses of csx/nkx2.5 mutants and their structure–function relationship
topic Full Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3685383/
work_keys_str_mv AT chenyunzi biochemicalanalysesofcsxnkx25mutantsandtheirstructurefunctionrelationship
AT yinghua biochemicalanalysesofcsxnkx25mutantsandtheirstructurefunctionrelationship
AT zhangjing biochemicalanalysesofcsxnkx25mutantsandtheirstructurefunctionrelationship
AT chengwei biochemicalanalysesofcsxnkx25mutantsandtheirstructurefunctionrelationship
AT kangyuanxi biochemicalanalysesofcsxnkx25mutantsandtheirstructurefunctionrelationship
AT huazichun biochemicalanalysesofcsxnkx25mutantsandtheirstructurefunctionrelationship