Proteomic analyses of Oryza sativa mature pollen reveal novel proteins associated with pollen germination and tube growth

被引:164
作者
Dai, S
Li, L
Chen, T
Chong, K
Xue, Y
Wang, T
机构
[1] Chinese Acad Sci, Inst Bot, Key Lab Photosynth & Environm Mol Physiol, Res Ctr Mol & Dev Biol, Beijing 100093, Peoples R China
[2] Chinese Acad Sci, Inst Genet & Dev Biol, Key Lab Mol & Dev Biol, Beijing, Peoples R China
关键词
mass spectrometry; mature pollen; Oryza sativa L;
D O I
10.1002/pmic.200401351
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
As a highly reduced organism, pollen performs specialized functions to generate and carry sperm into the ovule by its polarily growing pollen tube. Yet the molecular genetic basis of these functions is poorly understood. Here, we identified 322 unique proteins, most of which were not reported previously to be in pollen, from mature pollen of Oryza sativa L. ssp japonica using a proteomic approach, 23% of them having more than one isoform. Functional classification reveals that an over representation of the proteins was related to signal transduction (10%), wall remodeling and metabolism (11%), and protein synthesis, assembly and degradation (14%), as well as carbohydrate and energy metabolism (25%). Further, 11% of the identified proteins are functionally unknown and do not contain any conserved domain associated with known activities. These analyses also identified 5 novel proteins by de novo sequencing and revealed several important proteins, mainly involved in signal transduction (such as protein kinases, receptor kinase-interacting proteins, guanosine 5'-diphosphate dissociation inhibitors, C2 domain-containing proteins, cydophilins), protein synthesis, assembly and degradation (such as prohibitin, mitochondrial processing peptidase, putative UFD1, AAA(+) ATPase), and wall remodeling and metabolism (such as reversibly glycosylated polypeptides, cellulose synthase-like OsCsLF7). The study is the first dose investigation, to our knowledge, of protein complement in mature pollen, and presents useful molecular information at the protein level to further understand the mechanisms underlying pollen germination and tube growth.
引用
收藏
页码:2504 / 2529
页数:26
相关论文
共 70 条
[1]   Regulation of the pollen-specific actin-depolymerizing factor LIADF1 [J].
Allwood, EG ;
Anthony, RG ;
Smertenko, AP ;
Reichelt, S ;
Drobak, BK ;
Doonan, JH ;
Weeds, AG ;
Hussey, PJ .
PLANT CELL, 2002, 14 (11) :2915-2927
[2]   A GLYCOPROTEIN INHIBITOR OF PECTIN METHYLESTERASE IN KIWI FRUIT (ACTINIDIA-CHINENSIS) [J].
BALESTRIERI, C ;
CASTALDO, D ;
GIOVANE, A ;
QUAGLIUOLO, L ;
SERVILLO, L .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1990, 193 (01) :183-187
[3]   Transcriptional profiling of Arabidopsis tissues reveals the unique characteristics of the pollen transcriptome [J].
Becker, JD ;
Boavida, LC ;
Carneiro, J ;
Haury, M ;
Feijó, JA .
PLANT PHYSIOLOGY, 2003, 133 (02) :713-725
[4]   Cell wall proteins in apoplastic fluids of Arabidopsis thaliana rosettes:: Identification by mass spectrometry and bioinformatics [J].
Boudart, G ;
Jamet, E ;
Rossignol, M ;
Lafitte, C ;
Borderies, G ;
Jauneau, A ;
Esquerré-Tugayé, MT ;
Pont-Lezica, R .
PROTEOMICS, 2005, 5 (01) :212-221
[5]  
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
[6]   Translationally controlled tumor protein acts as a guanine nucleotide dissociation inhibitor on the translation elongation factor eEF1A [J].
Cans, C ;
Passer, BJ ;
Shalak, V ;
Nancy-Portebois, V ;
Crible, V ;
Amzallag, N ;
Allanic, D ;
Tufino, R ;
Argentini, M ;
Moras, D ;
Fiucci, G ;
Mirande, M ;
Amson, R ;
Telerman, A .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (24) :13892-13897
[7]   Actin-depolymerizing factor mediates Rac/Rop GTPase-regulated pollen tube growth [J].
Chen, CYH ;
Cheung, AY ;
Wu, HM .
PLANT CELL, 2003, 15 (01) :237-249
[8]   Temporal and spatial expression patterns of TUB9, a β-tubulin gene of Arabidopsis thaliana [J].
Cheng, ZG ;
Snustad, DP ;
Carter, JV .
PLANT MOLECULAR BIOLOGY, 2001, 47 (03) :389-398
[9]  
Chivasa S, 2002, ELECTROPHORESIS, V23, P1754, DOI 10.1002/1522-2683(200206)23:11&lt
[10]  
1754::AID-ELPS1754&gt