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A probable novel splicing isoform of human vascular endothelial growth factor / 南方医科大学学报
Journal of Southern Medical University ; (12): 755-759, 2012.
Article in English | WPRIM | ID: wpr-269003
ABSTRACT
<p><b>OBJECTIVE</b>To characterize a new alternative splicing isoform of human vascular endothelial growth factor (VEGF) gene.</p><p><b>METHODS</b>The total RNA was extracted from the lung tissue of a legally aborted 4-month-old fetus and amplified by RT-PCR. The amplified product was cloned into the plasmid pMD18-T and plasmid pcDNA3.1- for sequence analysis.</p><p><b>RESULTS</b>Electrophoresis of the RT-PCR products displayed one short band for VEGF(121) (487 bp) and a long band. The latter was characterized to contain two fragments one was normal VEGF(165) (619 bp), and the other (639 bp) had an identical nucleotide sequence to VEGF(165) with a 20 bp fragment inserted between exons 3 and 4. Sequence analysis showed that this 20-bp nucleotide was inserted from the 3' end of the third intron containing a splicing signal, thus causing shift mutation in the reading frame of VEGF gene and early appearance of the stop codon UAG in the middle of exon 4.</p><p><b>CONCLUSION</b>A new alternative splicing isoform of VEGF probably exists in the lung tissue of a legally aborted human fetus, and its biological significance remains to be further investigated.</p>
Subject(s)
Full text: Available Index: WPRIM (Western Pacific) Main subject: Gene Expression / Exons / Frameshift Mutation / Amino Acid Sequence / Classification / Alternative Splicing / Protein Isoforms / Reverse Transcriptase Polymerase Chain Reaction / Vascular Endothelial Growth Factor A / Genetics Limits: Humans Language: English Journal: Journal of Southern Medical University Year: 2012 Type: Article

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Full text: Available Index: WPRIM (Western Pacific) Main subject: Gene Expression / Exons / Frameshift Mutation / Amino Acid Sequence / Classification / Alternative Splicing / Protein Isoforms / Reverse Transcriptase Polymerase Chain Reaction / Vascular Endothelial Growth Factor A / Genetics Limits: Humans Language: English Journal: Journal of Southern Medical University Year: 2012 Type: Article