Abstract
Using a series of detailed experiments, Zhang and colleagues establish that the prostate cancer RNA chimera SLC45A3-ELK4 is generated by cis-splicing between the 2 adjacent genes and does not involve DNA rearrangements or trans-splicing. The chimera expression is induced by androgen treatment likely by overcoming the read-through block imposed by the intergenic CCCTC insulators bound by CCCTC-binding factor repressor protein. The chimeric transcript, but not wild-type ELK4, is shown to augment prostate cancer cell proliferation. © 2012 American Association for Cancer Research.
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CITATION STYLE
Kumar-Sinha, C., Kalyana-Sundaram, S., & Chinnaiyan, A. M. (2012). SLC45A3-ELK4 chimera in prostate cancer: Spotlight on cis-splicing. Cancer Discovery, 2(7), 582–585. https://doi.org/10.1158/2159-8290.CD-12-0212
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