Cloning and sequence analysis of Cu/Zn superoxide dismutase gene 2(MrSOD2) cDNA from Myrica rubra
Jing Lin
Abstract
Jing Lin
Abstract
A PCR-based homologous cloning strategy was used to identify superoxide dismutase(SOD) genes from the leaves of Myrica rubra.Results of sequence analysis indicated that a 233 bp cDNA with a conserved regions encoding a 77 amino acids actin ortholog was successfully cloned and characterized.The SOD contained the signature sequence of Cu/Zn-SOD gene family.Multiple alignment analysis of amino acid sequences of the putative SOD conserved regions in Myrica rubra was more than 86% homologous with the best scoring results from similarity searches of sequence databanks.This gene was named as MrSOD2(Genbank accession No.AB 661320).
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A PCR-based homologous cloning strategy was used to identify superoxide dismutase(SOD) genes from the leaves of Myrica rubra.Results of sequence analysis indicated that a 233 bp cDNA with a conserved regions encoding a 77 amino acids actin ortholog was successfully cloned and characterized.The SOD contained the signature sequence of Cu/Zn-SOD gene family.Multiple alignment analysis of amino acid sequences of the putative SOD conserved regions in Myrica rubra was more than 86% homologous with the best scoring results from similarity searches of sequence databanks.This gene was named as MrSOD2(Genbank accession No.AB 661320).
Key concepts: Myrica rubra, GenBank, Gene, Cloning (programming), Sequence analysis, Complementary DNA, Accession number (library science), Biology