Cloning and characterization of tomato leaf senescence-related cDNAs

被引:120
作者
John, I
Hackett, R
Cooper, W
Drake, R
Farrell, A
Grierson, D
机构
[1] UNIV NOTTINGHAM,DEPT PHYSIOL & ENVIRONM SCI,LOUGHBOROUGH LE12 5RD,LEICS,ENGLAND
[2] UNIV MICHIGAN,DEPT BIOL,ANN ARBOR,MI 48109
[3] NAT INST AGR BOT,CAMBRIDGE CB3 0LE,ENGLAND
[4] ZENECA PLANT SCI,JEALOTTS HILL RES STN,BRACKNELL RG42 6ET,BERKS,ENGLAND
基金
英国生物技术与生命科学研究理事会;
关键词
cDNA cloning; environmental factors; gene expression; leaf senescence; organs; tomato;
D O I
10.1023/A:1005746831643
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Senescence-related cDNA clones designated SENU 1, 4, 5 (senescence up-regulated) and SEND32, 33, 34, 35 and 36 (senescence down-regulated) isolated from a tomato leaf cDNA library [9] were characterized. Southern analysis showed that SEND32 is encoded by a single-copy gene while SEND33, 34, 35, 36 and SENU1 and SENU5 are members of small gene families. DNA and protein database searches revealed that SEND32, SEND35, SENU1 and SENU5 are novel cDNAs of unknown function. SEND33 encodes ferredoxin, SEND34 encodes a photosystem II 10 kDa polypeptide and SEND36 encodes catalase. The SENU4 sequence is identical to the P6 tomato protein previously reported to be pathogenesis-related [46]. The mRNA levels of SENU1, 4 and 5 increased during leaf senescence and SENU1 and SENU5 were also expressed at high levels during leaf development and in other plant organs. The SENU4 mRNA was associated more specifically with leaf senescence, although low expression was also detected in green fruit. The mRNAs for all SEND clones decreased during tomato leaf development and senescence and all except SEND32 were expressed at low levels in other plant organs. The accumulation of mRNA homologous to SENU4 and the decrease in abundance of SEND32 provide good molecular markers for leaf senescence.
引用
收藏
页码:641 / 651
页数:11
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