福建农林大学学报(自然科学版)
福建農林大學學報(自然科學版)
복건농림대학학보(자연과학판)
JOURNAL OF FUJIAN AGRICULTURE AND FORESTRY UNIVERSITY(NATURAL SCIENCE EDITION)
2009年
5期
507-511
,共5页
卢秉国%何炜毅%申艳红%蒋际谋%陈晓静%陈伟%吕柳新
盧秉國%何煒毅%申豔紅%蔣際謀%陳曉靜%陳偉%呂柳新
로병국%하위의%신염홍%장제모%진효정%진위%려류신
龙眼%子叶胚%3-磷酸甘油醛脱氢酶%基因克隆%序列分析
龍眼%子葉胚%3-燐痠甘油醛脫氫酶%基因剋隆%序列分析
용안%자협배%3-린산감유철탈경매%기인극륭%서렬분석
longan%cotyledon embryo%glyceraldehyde-3-phosphate dehydrogenase%gene cloning%sequence analysis
从龙眼子叶胚中分离得到一个大量表达的表达序列标签(EST),该EST编码序列与金鱼草3-磷酸甘油醛脱氢酶(GAPDH)基因的同源性为84%,利用cDNA末端快速扩增(RACE)技术成功克隆了龙眼GAPDH基因全长序列.序列分析表明,龙眼GAPDH基因的cDNA全长为1395 bp,包括一个长1008 bp、编码336个氨基酸的开放阅读框(ORF),5′端非编码区(UTR)长71 bp,3′-UTR长316 bp.龙眼GAPDH基因编码的氨基酸序列与水稻、葡萄、小果野蕉、拟南芥、银杏等GAPDH基因的氨基酸序列同源性均高达85%以上,该基因在GenBank中的登录号为FJ694011.
從龍眼子葉胚中分離得到一箇大量錶達的錶達序列標籤(EST),該EST編碼序列與金魚草3-燐痠甘油醛脫氫酶(GAPDH)基因的同源性為84%,利用cDNA末耑快速擴增(RACE)技術成功剋隆瞭龍眼GAPDH基因全長序列.序列分析錶明,龍眼GAPDH基因的cDNA全長為1395 bp,包括一箇長1008 bp、編碼336箇氨基痠的開放閱讀框(ORF),5′耑非編碼區(UTR)長71 bp,3′-UTR長316 bp.龍眼GAPDH基因編碼的氨基痠序列與水稻、葡萄、小果野蕉、擬南芥、銀杏等GAPDH基因的氨基痠序列同源性均高達85%以上,該基因在GenBank中的登錄號為FJ694011.
종용안자협배중분리득도일개대량표체적표체서렬표첨(EST),해EST편마서렬여금어초3-린산감유철탈경매(GAPDH)기인적동원성위84%,이용cDNA말단쾌속확증(RACE)기술성공극륭료용안GAPDH기인전장서렬.서렬분석표명,용안GAPDH기인적cDNA전장위1395 bp,포괄일개장1008 bp、편마336개안기산적개방열독광(ORF),5′단비편마구(UTR)장71 bp,3′-UTR장316 bp.용안GAPDH기인편마적안기산서렬여수도、포도、소과야초、의남개、은행등GAPDH기인적안기산서렬동원성균고체85%이상,해기인재GenBank중적등록호위FJ694011.
On the basis of one cDNA-AFLP expressed sequence tag (EST) from longan (Dimocarpus longan Lour. ) cotyledon embryos which is 84% homologous to Antirrhinum majus, the full length cDNA of glyceraldehyde-3-phosphate dehydrogenase (GAPDH) gene was cloned by rapid-amplification of cDNA ends (RACE). The gene consisted of 1395 bp encoding a protein of 336 amino acids, with 71 bp and 316 bp at 5' - UTR and 3' - UTR, respectively. The amino acid sequence comparison with the GAPDH gene of Oryza saliva, Vitis vinifera, Musa acuminata, Arabidopsis thaliana, and Ginkgo biloba showed that identity was all higher than 85%. The sequence was accepted and released by GenBank (accession number; FJ694011 ).