Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5589727 | Gene | 2017 | 37 Pages |
Abstract
Bax, a pro-apoptotic member of Bcl-2 family regulates apoptosis through homodimerization/heterodimerization with Bcl-2. Bax-α is the only product of the Bax gene that has been extensively studied. Bax-α exists in inactive form and several conformational changes are required during apoptosis to activate it. Here, we have identified a novel transcript variant of Bax gene in mouse which contains alternatively spliced new first exon that is different from the first exon of previously reported transcript. Conceptual translation of new transcript encodes a protein (Bax-α1), having different N-terminus. The existence of the new transcript variant was confirmed by reverse transcriptase-PCR, semi-nested PCR using primers designed for the newly identified transcript variant. The identity of PCR product obtained after semi-nested PCR was confirmed by DNA sequencing. Relative expression of new transcript variant with respect to reported transcript was also studied with the help of real time PCR. The existence of new transcript variant was further supported by the presence of clusters of overlapping ESTs from the database. Bax-α1 possibly displays heterogeneous properties as predicted by post-translational modification analysis tools. The differences in post-translational modifications might play important roles in divergent function of the new isoform. The three dimensional structure was generated by homology modelling to visualize the differences at N termini of known and newly identified variant.
Keywords
N-terminal methionine excisionRT PCRBcl-2qRT-PCRRMSDRXRαnMESemi-nested PCRSp1root-mean-square deviationdiscrete optimized protein energyBaxquantitative real time PCRmitochondrial outer membranetransmembraneB-cell lymphoma 2MoMTranscript variantHomology modellingBcl-2 homologyARTspecificity proteinDOPEglucocorticoid receptor
Related Topics
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Biochemistry, Genetics and Molecular Biology
Genetics
Authors
Mohammed Amir Husain, Hassan Mubarak Ishqi, Tarique Sarwar, Sayeed Ur Rehman, Mohammad Tabish,