Department of Biochemistry, AM University, Aligarh, Uttar Pradesh 202002, India.
Mol Cell Biochem. 2011 Nov;357(1-2):263-74. doi: 10.1007/s11010-011-0897-z. Epub 2011 Jun 3.
Prkar1a gene encodes regulatory type 1 alpha subunit (RIα) of cAMP-dependent protein kinase (PKA) in mouse. The role of this gene has been implicated in Carney complex and many cancer types that suggest its involvement in physiological processes like cell cycle regulation, growth and/or proliferation. We have identified and sequenced partial cDNA clones encoding four alternatively spliced transcripts of mouse Prkar1a gene. These transcripts have alternate 5' UTR structure which results from splicing of three exons (designated as E1a, E1b, and E1c) to canonical exon 2. The designated transcripts T1, T2, T3, and T4 contain 5' UTR exons as E1c, E1a + E1b, E1a, and E1b, respectively. The transcript T1 corresponded to earlier reported transcript in GenBank. In silico study of genomic DNA sequence revealed three distinct promoter regions namely, P1, P2, and P3 upstream of the exons E1a, E1b, and E1c, respectively. P1 is non-CpG-related promoter but P2 and P3 are CpG-related promoters; however, all three are TATA less. RT-PCR analysis demonstrated the expression of all four transcripts in late postnatal stages; however, these were differentially regulated in early postnatal stages of 0.5 day, 3 day, and 15 day mice in different tissue types. Variations in expression of Prkar1a gene transcripts suggest their regulation from multiple promoters that respond to a variety of signals arising in or out of the cell in tissue and developmental stage-specific manner.
Prkar1a 基因编码小鼠环磷酸腺苷依赖性蛋白激酶(PKA)的调节型 1 ɑ 亚基(RIα)。该基因的作用已被牵连到卡尼复合征和许多癌症类型中,这表明它参与了细胞周期调节、生长和/或增殖等生理过程。我们已经鉴定并测序了编码小鼠 Prkar1a 基因四个选择性剪接转录本的部分 cDNA 克隆。这些转录本具有不同的 5'UTR 结构,这是由于三个外显子(命名为 E1a、E1b 和 E1c)与典型外显子 2 拼接而产生的。指定的转录本 T1、T2、T3 和 T4 分别包含 5'UTR 外显子 E1c、E1a+E1b、E1a 和 E1b。转录本 T1 与 GenBank 中先前报道的转录本相对应。对基因组 DNA 序列的计算机研究揭示了三个不同的启动子区域,即 P1、P2 和 P3,分别位于外显子 E1a、E1b 和 E1c 的上游。P1 是非 CpG 相关的启动子,但 P2 和 P3 是 CpG 相关的启动子;然而,这三个启动子都没有 TATA 序列。RT-PCR 分析表明,所有四个转录本在出生后晚期都有表达;然而,在出生后 0.5 天、3 天和 15 天的不同组织类型中,这些转录本在早期的表达是不同的。Prkar1a 基因转录本表达的变化表明,它们的表达受到来自多个启动子的调控,这些启动子以组织和发育阶段特异性的方式响应细胞内外的各种信号。