Sucrose synthase localizes to cellulose synthesis sites in tracheary elements

被引:62
作者
Salnikov, VV
Grimson, MJ
Delmar, DP
Haigler, CH
机构
[1] Texas Tech Univ, Dept Biol Sci, Lubbock, TX 79409 USA
[2] Univ Calif Davis, Biol Sect, Davis, CA 95616 USA
关键词
Zinnia elegans; compositae; electron microscopic immunolocalization; freeze substitution; cellulose synthesis; sucrose synthase; actin; microtubule; tracheary element; secondary cell wall;
D O I
10.1016/S0031-9422(01)00045-0
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 synthesis of crystalline cellulose microfibrils in plants is a highly coordinated process that occurs at the interface of the cortex, plasma membrane, and cell wall. There is evidence that cellulose biogenesis is facilitated by the interaction of several proteins, but the details are just beginning to be understood. In particular. sucrose synthase, microtubules, and actin have been proposed to possibly associate with cellulose synthases (microfibril terminal complexes) in the plasma membrane. Differentiating tracheary elements of Zinnia elegans L. were used as a model system to determine the localization of sucrose synthase and actin in relation to the plasma membrane and its underlying microtubules during the deposition of patterned, cellulose-rich secondary walls. Cortical actin occurs with similar density both between and under secondary wall thickenings. In contrast, sucrose synthase is highly enriched near the plasma membrane and the microtubules under the secondary wall thickenings. Both actin and sucrose synthase lie closer to the plasma membrane: than the microtubules. These results show that the preferential localization of sucrose synthase at sites of high-rate cellulose synthesis can be generalized beyond cotton fibers, and they establish a spatial context for further work on a multi-protein complex that may facilitate secondary wall cellulose synthesis. (C) 2001 Elsevier science Ltd. All rights reserved.
引用
收藏
页码:823 / 833
页数:11
相关论文
共 41 条
[31]   FREEZE SUBSTITUTION AFTER FAST-FREEZE FIXATION IN PREPARATION FOR IMMUNOCYTOCHEMISTRY [J].
NICOLAS, MT ;
BASSOT, JM .
MICROSCOPY RESEARCH AND TECHNIQUE, 1993, 24 (06) :474-487
[32]   A ROUTINE FLAT EMBEDDING METHOD FOR ELECTRON-MICROSCOPY OF MICROORGANISMS ALLOWING SELECTION AND PRECISELY ORIENTATED SECTIONING OF SINGLE CELLS BY LIGHT-MICROSCOPY [J].
REYMOND, OL ;
PICKETTHEAPS, JD .
JOURNAL OF MICROSCOPY-OXFORD, 1983, 130 (APR) :79-84
[33]   TRACHEARY-ELEMENT DIFFERENTIATION IN SUSPENSION-CULTURED CELLS OF ZINNIA REQUIRES UPTAKE OF EXTRACELLULAR CA-2+ - EXPERIMENTS WITH CALCIUM-CHANNEL BLOCKERS AND CALMODULIN INHIBITORS [J].
ROBERTS, AW ;
HAIGLER, CH .
PLANTA, 1990, 180 (04) :502-509
[34]   RISE IN CHLOROTETRACYCLINE FLUORESCENCE ACCOMPANIES TRACHEARY ELEMENT DIFFERENTIATION IN SUSPENSION-CULTURES OF ZINNIA [J].
ROBERTS, AW ;
HAIGLER, CH .
PROTOPLASMA, 1989, 152 (01) :37-45
[35]   A SIMPLIFIED MEDIUM FOR INVITRO TRACHEARY ELEMENT DIFFERENTIATION IN MESOPHYLL SUSPENSION-CULTURES FROM ZINNIA-ELEGANS L [J].
ROBERTS, AW ;
KOONCE, LT ;
HAIGLER, CH .
PLANT CELL TISSUE AND ORGAN CULTURE, 1992, 28 (01) :27-35
[36]  
Seagull R. W., 1991, BIOSYNTHESIS BIODEGR, P143
[37]   THE EFFECTS OF MICROTUBULE AND MICROFILAMENT DISRUPTING AGENTS ON CYTOSKELETAL ARRAYS AND WALL DEPOSITION IN DEVELOPING COTTON FIBERS [J].
SEAGULL, RW .
PROTOPLASMA, 1990, 159 (01) :44-59
[38]   Identification of sucrose synthase as an actin-binding protein [J].
Winter, H ;
Huber, JL ;
Huber, SC .
FEBS LETTERS, 1998, 430 (03) :205-208
[39]   Regulation of sucrose metabolism in higher plants: Localization and regulation of activity of key enzymes [J].
Winter, H ;
Huber, SC .
CRITICAL REVIEWS IN PLANT SCIENCES, 2000, 19 (01) :31-67
[40]   Structure of the calcium pump from sarcoplasmic reticulum at 8-Å resolution [J].
Zhang, PJ ;
Toyoshima, C ;
Yonekura, K ;
Green, NM ;
Stokes, DL .
NATURE, 1998, 392 (6678) :835-839