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Two different unique cardiac isoforms of protein 4.1R in zebrafish, Danio rerio, and insights into their cardiac functions as related to their unique structures
Author(s) -
Murata Kenji,
Nunomura Wataru,
Takakuwa Yuichi,
Cherr Gary N.
Publication year - 2010
Publication title -
development, growth and differentiation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.864
H-Index - 66
eISSN - 1440-169X
pISSN - 0012-1592
DOI - 10.1111/j.1440-169x.2010.01195.x
Subject(s) - zebrafish , gene isoform , biology , alternative splicing , danio , microbiology and biotechnology , in situ hybridization , gene product , morpholino , gene , heart development , gene expression , actin , genetics , embryonic stem cell
Protein 4.1R (4.1R) has been identified as the major component of the human erythrocyte membrane skeleton. The members of the protein 4.1 gene family are expressed in a tissue‐specific alternative splicing manner that increases their functions in each tissue; however, the exact roles of cardiac 4.1R in the developing myocardium are poorly understood. In zebrafish (ZF), we identified two heart‐specific 4.1R isoforms, ZF4.1RH2 and ZF4.1RH3 , encoding N‐terminal 30 kDa (FERM) domain and spectrin‐actin binding domain (SABD) and C‐terminal domain (CTD), separately. Applying immunohistochemistry using specific antibodies for 30 kDa domain and CTD separately, the gene product of ZF4.1RH2 and ZF4.1RH3 appeared only in the ventricle and in the atrium, respectively, in mature hearts. During embryogenesis, both gene expressions are expressed starting 24 h post‐fertilization (hpf). Following whole‐mount in situ hybridization, ZF4.1RH3 gene expression was detected in the atrium of 37 hpf embryos. These results indicate that the gene product of ZF4.1RH3 is essential for normal morphological shape of the developing heart and to support the repetitive cycles of its muscle contraction and relaxation.