Molecular cloning and analysis of the 5'-flanking region of the rat PP1 alpha gene.
Ken Nomoto, Naoko Shibata, Kazuki Kitamura, Yusuke Mizuno, Kunimi Kikuchi
Abstract
Ken Nomoto, Naoko Shibata, Kazuki Kitamura, Yusuke Mizuno, Kunimi Kikuchi
Abstract
We have cloned an 8 kbp genomic fragment of 5'-flanking region of the gene encoding the catalytic subunit of rat protein phosphatase 1 alpha. Neither CAAT box nor TATA box was detected but a 300 bp high GC region containing nine Sp1 transcription factor binding sites is present immediately upstream of the translation start site, demonstrating that PP1 alpha is a housekeeping gene. Luciferase reporter assay showed that transcription of PP1 alpha is controlled at the high GC region.
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We have cloned an 8 kbp genomic fragment of 5'-flanking region of the gene encoding the catalytic subunit of rat protein phosphatase 1 alpha. Neither CAAT box nor TATA box was detected but a 300 bp high GC region containing nine Sp1 transcription factor binding sites is present immediately upstream of the translation start site, demonstrating that PP1 alpha is a housekeeping gene. Luciferase reporter assay showed that transcription of PP1 alpha is controlled at the high GC region.
Key concepts: TATA box, 5' flanking region, CAAT box, Housekeeping gene, Molecular biology, Gene, Biology, Promoter