Developmental changes in rat cardiac titin/connectin: Transitions in normal animals and in mutants with a delayed pattern of isoform transition

Marion L. Greaser, Paul R. Krzesinski, Chad M. Warren, Brian Kirkpatrick, Kenneth S. Campbell, Richard L. Moss

Producción científica: Articlerevisión exhaustiva

52 Citas (Scopus)

Resumen

Rat cardiac titin undergoes developmental changes in isoform expression during the period from late embryonic through the first 20-25 days of life. At least five size classes of titin isoforms have been identified using SDS agarose gel electrophoresis. The longest normal isoform is expressed in the embryonic stages, and it is progressively replaced with increasingly smaller versions. The isoform switching is consistent with changes in resting tension from lower values in one-day neonates to higher levels in adult myocytes. Considerable micro-heterogeneity in alternative splicing patterns also was found, particularly in the N2BA PEVK region of human, rat, and dog ventricle. A rat mutation has been identified in which the embryonic-neonatal titin isoform transitions are markedly delayed. These mutant animals may prove useful for examining the role of titin in stretch-activated signal transduction and in the Frank-Starling relationship.

Idioma originalEnglish
Páginas (desde-hasta)325-332
Número de páginas8
PublicaciónJournal of Muscle Research and Cell Motility
Volumen26
N.º6-8
DOI
EstadoPublished - dic 2005

Nota bibliográfica

Funding Information:
This work was supported by the College of Agricultural and Life Sciences, University of Wisconsin-Madison and by grants from the National Institutes of Health (HL47053; HL62466; HL77196).

Financiación

This work was supported by the College of Agricultural and Life Sciences, University of Wisconsin-Madison and by grants from the National Institutes of Health (HL47053; HL62466; HL77196).

FinanciadoresNúmero del financiador
National Institutes of Health (NIH)
College of Agricultural and Life Sciences, University of Wisconsin-Madison
National Heart, Lung, and Blood Institute Family Blood Pressure ProgramR01HL077196, P01HL047053, R01HL062466

    ASJC Scopus subject areas

    • Physiology
    • Biochemistry
    • Cell Biology

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