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Am J Physiol Cell Physiol (June 14, 2006). doi:10.1152/ajpcell.00198.2006
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Submitted on April 23, 2006
Accepted on June 2, 2006

Regulation of myosin light chain kinase and telokin expression in smooth muscle tissues

Brian Paul Herring1*, Omar El-Mounayri1, Patricia Jane Gallagher2, Feng Yin2, and Jiliang Zhou2

1 Cellular and Integrative Physiology, Indiana University School of Medicine, Indianapolis, Indiana, United States
2 Indianapolis, Indiana, United States; Cellular and Integrative Physiology, Indiana University School of Medicine, Indianapolis, Indiana, United States

* To whom correspondence should be addressed. E-mail: pherring{at}iupui.edu.

The mylk1 gene is a large gene spanning approximately 250kb, and comprising at least 31 exons. The mylk1 gene encodes at least 4 protein products, 2 isoforms of the 220 kDa myosin light chain kinase (MLCK), a 130 kDa MLCK and telokin. Transcripts encoding these products are derived from 4 independent promoters within the mylk1 gene. The kinases expressed from the mylk1 gene have been extensively characterized and function to regulate the activity of nonmuscle and smooth muscle myosin II. Activation of these myosin motors by MLCK modulates a variety of contractile processes, including smooth muscle contraction, cell adhesion, migration, and proliferation. Dysregulation of these processes contributes to a number of diseases. The non-catalytic gene product, telokin, has also been shown to modulate contraction in smooth muscle cells, through its ability to inhibit myosin light chain phosphatase. Given the crucial role of the products of the mylk1 gene in regulating numerous contractile processes, it seems intuitive that alterations in the transcriptional activity of the mylk1 gene will also have a significant impact on many physiological and pathological processes. In this review we highlight some of the recent studies that have described the transcriptional regulation of mylk1 gene products in smooth muscle tissues and discuss the implications of these findings for regulation of expression of other smooth muscle-specific genes.




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