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PMID: 12508222 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Heart-selective expression of the chicken FK506-binding protein (FKBP) 12.6 gene during embryonic development.

Yazawa S, Obata K, Iio A, Koide M, Yokota M, Sasaki S, Kagami H, Ono T

Abstract

FKBP12.6, a member of the family of FK506-binding proteins, selectively associates with the cardiac isoform of the ryanodine receptor and thereby stabilizes this Ca(2+) release channel. A chicken FKBP12.6 (chFKBP12.6) cDNA was cloned and shown to encode a protein of 108 amino acids. The deduced amino acid sequence of chFKBP12.6 is 91-92% identical to those of mammalian FKBP12.6 proteins. Northern blot analysis revealed that chFKBP12.6 mRNA is largely restricted to the heart during embryonic development and that the abundance of this mRNA in the heart decreases, and it becomes restricted to the atrium during cardiogenesis. In situ hybridization revealed that chFKBP12.6 mRNA is localized to the precardiac mesoderm before formation of the primitive heart tube. Expression of the chFKBP12.6 gene was initially apparent throughout the developing multichambered heart but became restricted to the atria before hatching. Reverse transcription and polymerase chain reaction analysis demonstrated that chFKBP12.6 mRNA is present in the embryo from early gastrulation and is most abundant immediately after the onset of the heartbeat. These observations suggest that the chFKBP12.6 gene is expressed before heart morphogenesis to play a role in excitation-contraction coupling in cardiomyocytes and that the function of the encoded protein becomes increasingly restricted to the atrium during embryonic development.

MeSH Terms
Amino Acid Sequence Animals Base Sequence Blotting, Northern Chick Embryo Cloning, Molecular DNA, Complementary/metabolism Gene Expression Regulation, Developmental Heart/embryology Humans In Situ Hybridization Molecular Sequence Data Myocardium/cytology RNA, Messenger/metabolism Reverse Transcriptase Polymerase Chain Reaction Sequence Homology, Amino Acid Tacrolimus Binding Proteins/biosynthesis Time Factors
Chemicals
DNA, Complementary RNA, Messenger Tacrolimus Binding Proteins
Authors & Affiliations
8 authors, click to expand affiliations / ORCID
Yazawa Shigenobu
United Graduate School of Agricultural Science, Gifu University, Gifu, Japan.
Obata Koji
Iio Akio
Koide Masafumi
Yokota Mitsuhiro
Sasaki Shin-Ichi
Kagami Hiroshi
Ono Tamao
Article Info
Journal
Developmental dynamics : an official publication of the American Association of Anatomists
Abbr.
Dev Dyn
ISSN
1058-8388
Published
2003-01-00
Pages
33-41
Language
English
Region
United States
NLM ID
9201927
Subset
IM
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