Identification, basic characterization and evolutionary analysis of differentially spliced mRNA isoforms of human YAP1 gene

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• 作者：Christian J. Gaffney ; Tsutomu Oka ; Virginia Mazack ; Dror Hilman ; Uri Gat ; Tomoki Muramatsu ; Johji Inazawa ; Alicia Golden ; David J. Carey ; Amjad Farooq ; Gerard Tromp ; Marius Sudol
• 关键词：bp ; base pair ; cDNA ; DNA complementary to RNA ; PCR ; polymerase chain reaction ; WW domain ; tryptophan&ndash ; tryptophan domain
• 刊名：Gene
• 出版年：2012
• 出版时间：10 November, 2012
• 年：2012
• 卷：509
• 期：2
• 页码：215-222
• 全文大小：1082 K

文摘

The YAP1 gene encodes a potent new oncogene and stem cell factor. However, in some cancers, the YAP1 gene plays a role of tumor suppressor. At present, the gene and its products are intensely studied and its cDNAs are used as transgenes in cellular and animal models. Here, we report 4 new potential mRNA splicing isoforms of the YAP1 gene, bringing the total number of isoforms to 8. We detected all 8 YAP1 isoforms in a panel of human tissues and evaluated the expression of the longest isoform of YAP1 (YAP1-2¦Ä) using Real Time PCR. All YAP1 isoforms are barely detectable in human leukocytes compared to fair levels of expression found in other human tissues. We analyzed the structure of the genomic region that gave rise to alternatively spliced YAP1 transcripts in different metazoans. We found that YAP1 isoforms, which utilize exon 6 emerged in evolution with the appearance of amniotes. Interestingly, 6 YAP1 isoforms, which contain the exon 5 extension, exon 6 or both would have their leucine zipper region disrupted in the predicted protein product, compared to the intact leucine zipper found in two YAP1 (¦Á) isoforms. This observation has direct functional ramifications for YAP1 signaling. We also propose a normalized nomenclature for the mRNA splice variants of the YAP1 gene, which should aid in the characterization of signaling differences among the potential protein products of the YAP1 gene.