摘要
Differential display reverse transcription-PCR method was utilized to analyze the differential expression genes in different Arabidopsis ecotypes after inoculating Botrytis cinerea.Total 150 differentially expressed cDNA fragments were obtained,49 cDNA fragments were found to hybridize to cDNA and 5 cDNA fragments were cloned and then sequenced among them.Three fragments displayed high homology(96.1%,99.6% and 100.0%) to phosphatidylinositol transfer-like protein IV(Sec14p protein),TAC clone K9I9 and NADH-dehydrogenase subunit 4L of Arabidopsis thaliana,while alignment with NCBI databases using BLAST program.It was speculated that these fragments might relate to disease-resistance of Arabidopsis to B.cinerea.
Differential display reverse transcription-PCR method was utilized to analyze the differential expression genes in different Arabidopsis ecotypes after inoculating Botrytis cinerea. Total 150 differentially expressed cDNA fragments were obtained, 49 cDNA fragments were found to hybridize to cDNA and 5 cDNA fragments were cloned and then sequenced among them. Three fragments displayed high homology (96.1%, 99.6% and 100.0% ) to phosphatidylinositol transfer-like protein IV (Secl4p protein), TAC clone K919 and NADH-dehydrogenase subunit 4L of Arabidopsis thaliana, while alignment with NCBI databases using BLAST program. It was speculated that these fragments might relate to disease-resistance of Arabidopsis to B. cinerea.
出处
《植物病理学报》
CAS
CSCD
北大核心
2006年第6期562-565,共4页
Acta Phytopathologica Sinica
基金
河北农业大学"9816"科技重点项目资助