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Suppression of atrial myosin gene expression occurs independently in the left and right ventricles of the developing mouse heart

✍ Scribed by Peter S. Zammit; Robert G. Kelly; Diego Franco; Nigel Brown; Antoon F.M. Moorman; Margaret E. Buckingham


Publisher
John Wiley and Sons
Year
2000
Tongue
English
Weight
863 KB
Volume
217
Category
Article
ISSN
1058-8388

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✦ Synopsis


Many cardiac genes are broadly expressed in the early heart and become restricted to the atria or ventricles as development proceeds. Additional transcriptional differences between left and right compartments of the embryonic heart have been described recently, in particular for a number of transgenes containing cardiac regulatory elements. We now demonstrate that three myosin genes which become transcriptionally restricted to the atria between embryonic day (E) 12.5 and birth, ␣-myosin heavy chain (MHC), myosin light chain (MLC) 1A and MLC2A, are coordinately downregulated in the compact myocardium of the left ventricle before that of the right ventricle. ␣-MHC protein also accumulates in the right, but not left, compact ventricular myocardium during this period, suggesting that this transient regionalisation contributes to foetal heart function. dHAND and eHAND, basic helix-loop-helix transcription factors known to be expressed in the right and left ventricles respectively at E10.5, remain regionalised between E12.5 and E14.5. Downregulation of ␣-MHC, MLC1A, and MLC2A in iv/iv embryos, which have defective left/right patterning, initiates in the morphological left (systemic) ventricle regardless of its anatomical position on the right or left hand side of the heart. This points to the importance of left/ right ventricular differences in sarcomeric gene expression patterns during foetal cardiogenesis and indicates that these differences originate in the embryo in response to anterior-posterior patterning of the heart tube rather than as a result of cardiac looping.


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## Abstract A central problem in neurobiology is the elucidation of the mechanisms that underlie left–right asymmetries in brain structure and function. Using a transcriptome screening approach, we found asymmetric gene expression patterns in the right when compared with the left hippocampal format