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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...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Molecular Diversity Preservation International (MDPI)
2007
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3685383/ |
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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/ |
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