2007•Acta Horticulturae SinicaRequires access

Cloning and Sequence Analysis of Chinese Cabbage Chitinase Gene CHB4

Jun Fan

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Abstract

Based on the conserved sequence of the chitinase of crucifers,about 1 kb DNA fragment and 5'-end fragment(150 bp)were amplified by PCR from genomic DNA of Chinese cabbage.Experiments were performed on 7-day-old Chinese cabbage seedlings after germination with salicylic acid of different concentrations.Total RNA was prepared from the plant with higher chitinase activity,and 3'-end fragment was amplified by 3' RACE.Comparing Chinese cabbage chitinase sequence cloned in this experiment with that reported in GenBank composed of 1 094 bp nucleotide of Brassica napus,the experiment showed that the chitinase sequence of Chinese cabbage is 1 517 bp in size with one intron of 508 bp(DDBJ accession number:AB257452),and shares as high as 99% identity with B.napus and over 50% with other high plants in coding region.

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What this paper is about

Based on the conserved sequence of the chitinase of crucifers,about 1 kb DNA fragment and 5'-end fragment(150 bp)were amplified by PCR from genomic DNA of Chinese cabbage.Experiments were performed on 7-day-old Chinese cabbage seedlings after germination with salicylic acid of different concentrations.Total RNA was prepared from the plant with higher chitinase activity,and 3'-end fragment was amplified by 3' RACE.Comparing Chinese cabbage chitinase sequence cloned in this experiment with that reported in GenBank composed of 1 094 bp nucleotide of Brassica napus,the experiment showed that the chitinase sequence of Chinese cabbage is 1 517 bp in size with one intron of 508 bp(DDBJ accession number:AB257452),and shares as high as 99% identity with B.napus and over 50% with other high plants in coding region.

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Available abstract

Based on the conserved sequence of the chitinase of crucifers,about 1 kb DNA fragment and 5'-end fragment(150 bp)were amplified by PCR from genomic DNA of Chinese cabbage.Experiments were performed on 7-day-old Chinese cabbage seedlings after germination with salicylic acid of different concentrations.Total RNA was prepared from the plant with higher chitinase activity,and 3'-end fragment was amplified by 3' RACE.Comparing Chinese cabbage chitinase sequence cloned in this experiment with that reported in GenBank composed of 1 094 bp nucleotide of Brassica napus,the experiment showed that the chitinase sequence of Chinese cabbage is 1 517 bp in size with one intron of 508 bp(DDBJ accession number:AB257452),and shares as high as 99% identity with B.napus and over 50% with other high plants in coding region.

Key concepts: GenBank, Chitinase, Biology, Gene, genomic DNA, Accession number (library science), Genetics, Coding region

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