Key result
Fast skeletal troponin I, fast skeletal troponin T, and slow skeletal-cardiac troponin C genes are transcriptionally coactivated during skeletal myoblast differentiation in Japanese quail.
Early troponin gene coactivation in quail myogenesis; leaves open applicability to human cardiac development or disease.
We compared the developmental regulation of the three troponin genes that encode the proteins of the Ca2+ regulatory complex in striated muscles of the Japanese quail. Nuclear run-on transcription and RNA protection analyses showed that the fast skeletal troponin I, the fast skeletal troponin T, and the slow skeletal-cardiac troponin C genes were transcriptionally coactivated and that transcripts rapidly accumulated within 6 to 12 h after the initiation of myoblast differentiation. The fast-isoform mRNAs of troponin I and troponin T were coexpressed at similar levels in different skeletal muscles, whereas the slow-cardiac troponin C mRNA varied independently and was the only one of these genes expressed in embryonic and adult heart. We conclude that these troponin genes are transcriptionally coactivated during skeletal myoblast differentiation, indicating that their transcription is under precise temporal control. However, this troponin C gene is regulated independently is specialized striated muscles.
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Bucher et al. (1988) studied this question. Myoblast differentiation was evaluated on Developmental regulation and transcriptional coactivation of troponin genes. Fast skeletal troponin I, fast skeletal troponin T, and slow skeletal-cardiac troponin C genes are transcriptionally coactivated during skeletal myoblast differentiation in Japanese quail.
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