Differential regulation of Hand1 homodimer and Hand1-E12 heterodimer activity by the cofactor FHL2.

The basic helix-loop-helix (bHLH) factor Hand1 plays an essential role in cardiac morphogenesis, and yet its precise function remains unknown. Protein-protein interactions involving Hand1 provide a means of determining how Hand1-induced gene expression in the developing heart might be regulated. Han...

Descrición completa

Detalles Bibliográficos
Main Authors: Hill, A, Riley, P
Formato: Journal article
Idioma:English
Publicado: 2004
_version_ 1826261026191966208
author Hill, A
Riley, P
author_facet Hill, A
Riley, P
author_sort Hill, A
collection OXFORD
description The basic helix-loop-helix (bHLH) factor Hand1 plays an essential role in cardiac morphogenesis, and yet its precise function remains unknown. Protein-protein interactions involving Hand1 provide a means of determining how Hand1-induced gene expression in the developing heart might be regulated. Hand1 is known to form either heterodimers with near-ubiquitous E-factors and other lineage-restricted class B bHLH proteins or homodimers with itself in vitro. To date, there have been no reported Hand1 protein interactions involving non-bHLH proteins. Heterodimer-versus-homodimer choice is mediated by the phosphorylation status of Hand1; however, little is known about the in vivo function of these dimers or, importantly, how they are regulated. In an effort to understand how Hand1 activity in the heart might be regulated postdimerization, we have investigated tertiary Hand1-protein interactions with non-bHLH factors. We describe a novel interaction of Hand1 with the LIM domain protein FHL2, a known transcriptional coactivator and corepressor expressed in the developing cardiovascular system. FHL2 interacts with Hand1 via the bHLH domain and is able to repress Hand1/E12 heterodimer-induced transcription but has no effect on Hand1/Hand1 homodimer activity. This effect of FHL2 is not mediated either at the level of dimerization or via an effect of Hand1/E12 DNA binding. In summary, our data describe a novel differential regulation of Hand1 heterodimers versus homodimers by association of the cofactor FHL2 and provide insight into the potential for a tertiary level of control of Hand1 activity in the developing heart.
first_indexed 2024-03-06T19:15:03Z
format Journal article
id oxford-uuid:180d83fb-6936-484f-b38c-eff181654965
institution University of Oxford
language English
last_indexed 2024-03-06T19:15:03Z
publishDate 2004
record_format dspace
spelling oxford-uuid:180d83fb-6936-484f-b38c-eff1816549652022-03-26T10:41:11ZDifferential regulation of Hand1 homodimer and Hand1-E12 heterodimer activity by the cofactor FHL2.Journal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:180d83fb-6936-484f-b38c-eff181654965EnglishSymplectic Elements at Oxford2004Hill, ARiley, PThe basic helix-loop-helix (bHLH) factor Hand1 plays an essential role in cardiac morphogenesis, and yet its precise function remains unknown. Protein-protein interactions involving Hand1 provide a means of determining how Hand1-induced gene expression in the developing heart might be regulated. Hand1 is known to form either heterodimers with near-ubiquitous E-factors and other lineage-restricted class B bHLH proteins or homodimers with itself in vitro. To date, there have been no reported Hand1 protein interactions involving non-bHLH proteins. Heterodimer-versus-homodimer choice is mediated by the phosphorylation status of Hand1; however, little is known about the in vivo function of these dimers or, importantly, how they are regulated. In an effort to understand how Hand1 activity in the heart might be regulated postdimerization, we have investigated tertiary Hand1-protein interactions with non-bHLH factors. We describe a novel interaction of Hand1 with the LIM domain protein FHL2, a known transcriptional coactivator and corepressor expressed in the developing cardiovascular system. FHL2 interacts with Hand1 via the bHLH domain and is able to repress Hand1/E12 heterodimer-induced transcription but has no effect on Hand1/Hand1 homodimer activity. This effect of FHL2 is not mediated either at the level of dimerization or via an effect of Hand1/E12 DNA binding. In summary, our data describe a novel differential regulation of Hand1 heterodimers versus homodimers by association of the cofactor FHL2 and provide insight into the potential for a tertiary level of control of Hand1 activity in the developing heart.
spellingShingle Hill, A
Riley, P
Differential regulation of Hand1 homodimer and Hand1-E12 heterodimer activity by the cofactor FHL2.
title Differential regulation of Hand1 homodimer and Hand1-E12 heterodimer activity by the cofactor FHL2.
title_full Differential regulation of Hand1 homodimer and Hand1-E12 heterodimer activity by the cofactor FHL2.
title_fullStr Differential regulation of Hand1 homodimer and Hand1-E12 heterodimer activity by the cofactor FHL2.
title_full_unstemmed Differential regulation of Hand1 homodimer and Hand1-E12 heterodimer activity by the cofactor FHL2.
title_short Differential regulation of Hand1 homodimer and Hand1-E12 heterodimer activity by the cofactor FHL2.
title_sort differential regulation of hand1 homodimer and hand1 e12 heterodimer activity by the cofactor fhl2
work_keys_str_mv AT hilla differentialregulationofhand1homodimerandhand1e12heterodimeractivitybythecofactorfhl2
AT rileyp differentialregulationofhand1homodimerandhand1e12heterodimeractivitybythecofactorfhl2