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Open AccessJournal ArticleDOI

Sequential activation of alpha-actin genes during avian cardiogenesis: vascular smooth muscle alpha-actin gene transcripts mark the onset of cardiomyocyte differentiation.

D L Ruzicka, +1 more
- 01 Dec 1988 - 
- Vol. 107, Iss: 6, pp 2575-2586
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TLDR
The specific expression of the vascular smooth muscle alpha- actin gene marks the onset of differentiation of cardiac cells and represents the first demonstration of coexpression of both smooth muscle and striated alpha-actin genes within myogenic cells.
Abstract
The expression of cytoplasmic beta-actin and cardiac, skeletal, and smooth muscle alpha-actins during early avian cardiogenesis was analyzed by in situ hybridization with mRNA-specific single-stranded DNA probes. The cytoplasmic beta-actin gene was ubiquitously expressed in the early chicken embryo. In contrast, the alpha-actin genes were sequentially activated in avian cardiac tissue during the early stages of heart tube formation. The accumulation of large quantities of smooth muscle alpha-actin transcripts in epimyocardial cells preceded the expression of the sarcomeric alpha-actin genes. The accumulation of skeletal alpha-actin mRNAs in the developing heart lagged behind that of cardiac alpha-actin by several embryonic stages. At Hamburger-Hamilton stage 12, the smooth muscle alpha-actin gene was selectively down-regulated in the heart such that only the conus, which subsequently participates in the formation of the vascular trunks, continued to express this gene. This modulation in smooth muscle alpha-actin gene expression correlated with the beginning of coexpression of sarcomeric alpha-actin transcripts in the epimyocardium and the onset of circulation in the embryo. The specific expression of the vascular smooth muscle alpha-actin gene marks the onset of differentiation of cardiac cells and represents the first demonstration of coexpression of both smooth muscle and striated alpha-actin genes within myogenic cells.

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microRNA-133a regulates cardiomyocyte proliferation and suppresses smooth muscle gene expression in the heart

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Acquisition of the contractile phenotype by murine arterial smooth muscle cells depends on the Mir143/145 gene cluster

TL;DR: It is demonstrated that the mouse miR-143/145 cluster, expression of which is confined to SMCs during development, is required for VSMC acquisition of the contractile phenotype and manipulated expression may offer a new approach for influencing vascular repair and attenuating arteriosclerosis pathogenesis.
References
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Journal ArticleDOI

A series of normal stages in the development of the chick embryo

TL;DR: In this article, a series of normal stages of the chick embryo is described in terms of the length of time of incubation, except for the first three days during which more detailed characteristics such as the number of somites are applied.
Journal ArticleDOI

Detection of mRNAs in sea urchin embryos by in situ hybridization using asymmetric RNA probes

TL;DR: Estimates from the observed signals indicate that a large fraction of target RNAs is both retained in sections and hybridized with probe at saturation, and coupled with measurements of nonspecific background binding of heterologous probes, these data indicate that the method has sufficient sensitivity to detect many moderately abundant mRNAs.
Journal ArticleDOI

Quantitative analysis of in situ hybridization methods for the detection of actin gene expression.

TL;DR: An efficient, quantitative approach for the optimization of in situ hybridization using double-stranded recombinant DNA probes, which is simpler and less destructive to cellular RNA and morphology than other protocols.
Journal ArticleDOI

Embryonic development of the heart. I. A light and electron microscopic study of myocardial development in the early chick embryo

TL;DR: Embryonic chick myocardium (stages 8+ to 12−) was studied by light and electron microscopy and the amount of granular reticulum contained in the myocardial cell cytoplasm is large and suggests that these cells may have a secretory function.
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