Literature DB >> 12297046

Modulation of cardiac growth and development by HOP, an unusual homeodomain protein.

Chong Hyun Shin1, Zhi-Ping Liu, Robert Passier, Chun-Li Zhang, Da-Zhi Wang, Thomas M Harris, Hiroyuki Yamagishi, James A Richardson, Geoffrey Childs, Eric N Olson.   

Abstract

We have discovered an unusual homeodomain protein, called HOP, which is comprised simply of a homeodomain. HOP is highly expressed in the developing heart where its expression is dependent on the cardiac-restricted homeodomain protein Nkx2.5. HOP does not bind DNA and acts as an antagonist of serum response factor (SRF), which regulates the opposing processes of proliferation and myogenesis. Mice homozygous for a HOP null allele segregate into two phenotypic classes characterized by an excess or deficiency of cardiac myocytes. We propose that HOP modulates SRF activity during heart development; its absence results in an imbalance between cardiomyocyte proliferation and differentiation with consequent abnormalities in cardiac morphogenesis.

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Year:  2002        PMID: 12297046     DOI: 10.1016/s0092-8674(02)00933-9

Source DB:  PubMed          Journal:  Cell        ISSN: 0092-8674            Impact factor:   41.582


  85 in total

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7.  Ablation of Nkx2-5 at mid-embryonic stage results in premature lethality and cardiac malformation.

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8.  Cardiac hypertrophy and histone deacetylase-dependent transcriptional repression mediated by the atypical homeodomain protein Hop.

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