UP-REGULATION OF A CYSTEINE PROTEASE ACCOMPANIES THE ETHYLENE-INSENSITIVE SENESCENCE OF DAYLILY (HEMEROCALLIS) FLOWERS

被引:102
作者
VALPUESTA, V
LANGE, NE
GUERRERO, C
REID, MS
机构
[1] UNIV CALIF DAVIS,DEPT ENVIRONM HORT,DAVIS,CA 95616
[2] UNIV MALAGA,DEPT BIOQUIM & BIOL MOLEC,E-29071 MALAGA,SPAIN
关键词
DAYLILY; ETHYLENE-INSENSITIVE SENESCENCE; FLOWER SENESCENCE; HEMEROCALLIS; CYSTEINE PROTEASE;
D O I
10.1007/BF00020403
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
The flowers of daylily (Hemerocallis x hybrida cv. Cradle Song) open at midnight, start to senesce 12 h later, and are completely senescent by the following midnight. Differential screening of a cDNA library constructed from tepals of flowers showing incipient senescence revealed 25 clones that were strongly up-regulated in senescent tepals. Re-screening and interactive Southern analysis of these clones revealed 3 families of up-regulated clones. Transcripts of one clone, SEN10, were not detectable at midnight, but increased dramatically as senescence proceeded. The derived amino acid sequence of the full-length cDNA (SEN102) has strong homology with cysteine proteases that have been reported from other plant tissues. The sequence contains a secretory signal peptide and a probable prosequence upstream of the mature protein. Amino acids critical to the active site and structure of cysteine proteases are conserved, and the C-terminus of the polypeptide has a unique putative endoplasmic reticulum retention signal -RDEL.
引用
收藏
页码:575 / 582
页数:8
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