Computational prediction and characterisation of ubiquitously expressed new splice variant of Prkaca gene in mouse

被引:4
作者
Banday, Abdul Rouf [1 ]
Azim, Shafquat [1 ]
Hussain, Mohammed Aamir [1 ]
Nehar, Shamshun [2 ]
Tabish, Mohammad [1 ]
机构
[1] Amity Univ, Fac Life Sci, Dept Biochem, Aligarh 202002, Uttar Pradesh, India
[2] Ranchi Univ, PG Dept Zool, Ranchi 834008, Jharkhand, India
关键词
bioinformatics tools; exon(s); N-terminal variants; prediction; splicing; DEPENDENT PROTEIN-KINASE; CATALYTIC-SUBUNIT; C-BETA; MOLECULAR CHARACTERIZATION; MULTIPLE TRANSCRIPTS; ISOFORM; ALPHA; IDENTIFICATION; EXONS; DNA;
D O I
10.1002/cbin.10080
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Prkaca gene of mouse encodes for a cAMP dependent protein kinase catalytic alpha subunit. PKA occurs naturally as a 4-membered structure having two regulatory (R) and two catalytic (C) subunits each encoded by separate gene. Alternatively spliced two transcript variants are known for the Prkaca gene, which encode for two isoforms of PKA C-subunits, namely C1 and C2. These isoforms arise as a result of alternative splicing of the first coding exon with the internal exons. We have identified a new transcript variant using combinatorial approach of bioinformatics and molecular biology techniques involving RT-PCR, semi-nested PCR and sequencing. The new transcript variant encoding C3 isoform has N-terminus that differs from C1 and C2 isoforms. C3 isoform also arise as a result of alternative splicing of first coding exon with the internal exon. Newly identified transcript is expressed ubiquitously in different tissues examined.
引用
收藏
页码:687 / 693
页数:7
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