Genes involved in osmoregulation during turgor-driven cell expansion of developing cotton fibers are differentially regulated

被引:145
作者
Smart, LB
Vojdani, F
Maeshima, M
Wilkins, TA [1 ]
机构
[1] Lawrence Livermore Natl Lab, Dept Agron & Range Sci, Livermore, CA 95616 USA
[2] Lawrence Livermore Natl Lab, Dept Vegetable Crops, Livermore, CA 95616 USA
[3] Nagoya Univ, Grad Sch Bioagr Sci, Nagoya, Aichi, Japan
关键词
D O I
10.1104/pp.116.4.1539
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Cotton (Gossypium hirsutum L.) fibers are single-celled trichomes that synchronously undergo a phase of rapid cell expansion, then a phase including secondary cell wall deposition, and finally maturation. To determine if there is coordinated regulation of gene expression during fiber expansion, we analyzed the expression of components involved in turgor regulation and a cytoskeletal protein by measuring levels of mRNA and protein accumulation and enzyme activity. Fragments of the genes for the plasma membrane proton-translocating ATPase, vacuole-ATPase, proton-translocating pyrophosphatase (PPase), phosphoenolpyruvate carboxylase, major intrinsic protein, and cu-tubulin were amplified by polymerase chain reaction and used as probes in ribonuclease protection assays of RNA from a fiber developmental series, revealing two discrete patterns of mRNA accumulation. Transcripts of all but the PPase accumulated to highest levels during the period of peak expansion (+12-15 d postanthesis [dpa]), then declined with the onset of secondary cell wall synthesis. The PPase was constitutively expressed through fiber development. Activity of the two proton-translocating-ATPases peaked at +15 dpa, whereas PPase activity peaked at +20 dpa, suggesting that all are involved in the process of cell expansion but with varying roles. Patterns of protein accumulation and enzyme activity for some of the proteins examined suggest posttranslational regulation through fiber development.
引用
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页码:1539 / 1549
页数:11
相关论文
共 55 条
[1]   STRUCTURE AND EXPRESSION OF A SUGARCANE GENE ENCODING A HOUSEKEEPING PHOSPHOENOLPYRUVATE CARBOXYLASE [J].
ALBERT, HA ;
MARTIN, T ;
SUN, SSM .
PLANT MOLECULAR BIOLOGY, 1992, 20 (04) :663-671
[2]  
Ames BN., 1966, Methods in Enzymology, P115, DOI DOI 10.1016/0076-6879(66)08014-5
[3]   Physiology of ion transport across the tonoplast of higher plants [J].
Barkla, BJ ;
Pantoja, O .
ANNUAL REVIEW OF PLANT PHYSIOLOGY AND PLANT MOLECULAR BIOLOGY, 1996, 47 :159-184
[4]   DEVELOPMENT OF THE COTTON FIBER [J].
BASRA, AS ;
MALIK, CP .
INTERNATIONAL REVIEW OF CYTOLOGY-A SURVEY OF CELL BIOLOGY, 1984, 89 :65-113
[5]   H+-ATPASE ACTIVITY FROM STORAGE TISSUE OF BETA-VULGARIS .2. H+-ATP STOICHIOMETRY OF AN ANION-SENSITIVE H+-ATPASE [J].
BENNETT, AB ;
SPANSWICK, RM .
PLANT PHYSIOLOGY, 1984, 74 (03) :545-548
[6]   H+-ATPASE ACTIVITY FROM STORAGE TISSUE OF BETA-VULGARIS .1. IDENTIFICATION AND CHARACTERIZATION OF AN ANION-SENSITIVE H+-ATPASE [J].
BENNETT, AB ;
ONEILL, SD ;
SPANSWICK, RM .
PLANT PHYSIOLOGY, 1984, 74 (03) :538-544
[7]  
BENNETT AB, 1988, METHODS ENZYMOL, V157, P579
[8]  
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
[9]   Phosphoenolpyruvate carboxylase: A ubiquitous, highly regulated enzyme in plants [J].
Chollet, R ;
Vidal, J ;
OLeary, MH .
ANNUAL REVIEW OF PLANT PHYSIOLOGY AND PLANT MOLECULAR BIOLOGY, 1996, 47 :273-298
[10]   AQUAPORINS - WATER CHANNEL PROTEINS OF PLANT AND ANIMAL-CELLS [J].
CHRISPEELS, MJ ;
AGRE, P .
TRENDS IN BIOCHEMICAL SCIENCES, 1994, 19 (10) :421-425