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Letter

Defining the mammalian CArGome

¹ Cardiovascular Research Institute, University of Rochester School of Medicine, Rochester, New York 14642, USA ² Center for Bioinformatics, University of Pennsylvania, Philadelphia, Pennsylvania 19104, USA ³ Department of Bioengineering, University of Pennsylvania, Philadelphia, Pennsylvania 19104, USA ⁴ Department of Genetics, University of Pennsylvania, Philadelphia, Pennsylvania 19104, USA

Serum response factor (SRF) binds a 1216-fold degenerate cis element known as the CArG box. CArG boxes are found primarily in muscle- and growth-factor-associated genes although the full spectrum of functional CArG elements in the genome (the CArGome) has yet to be defined. Here we describe a genome-wide screen to further define the functional mammalian CArGome. A computational approach involving comparative genomic analyses of human and mouse orthologous genes uncovered >100 hypothetical SRF-dependent genes, including 10 previously identified SRF targets, harboring a conserved CArG element within 4000 bp of the annotated transcription start site (TSS). We PCR-cloned 89 hypothetical SRF targets and subjected each of them to at least two of several validations including luciferase reporter, gel shift, chromatin immunoprecipitation, and mRNA expression following RNAi knockdown of SRF; 60/89 (67%) of the targets were validated. Interestingly, 26 of the validated SRF target genes encode for cytoskeletal/contractile or adhesion proteins. RNAi knockdown of SRF diminishes expression of several SRF-dependent cytoskeletal genes and elicits an attending perturbation in the cytoarchitecture of both human and rodent cells. These data illustrate the power of integrating existing algorithms to interrogate the genome in a relatively unbiased fashion for cis-regulatory element discovery. In this manner, we have further expanded the mammalian CArGome with the discovery of an array of cyto-contractile genes that coordinate normal cytoskeletal homeostasis. We suggest one function of SRF is that of an ancient master regulator of the actin cytoskeleton.

⁵ These authors contributed equally to this work.

⁶ Corresponding author.
E-mail j.m.miano{at}rochester.edu; fax (585) 273-1497.

[Supplemental material is available online at www.genome.org.]

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