Distinct localization of two closely related Ypt3/Rab11 proteins on the trafficking pathway in higher plants

被引:49
作者
Inaba, T [1 ]
Nagano, Y [1 ]
Nagasaki, T [1 ]
Sasaki, Y [1 ]
机构
[1] Nagoya Univ, Grad Sch Agr Sci, Lab Plant Mol Biol, Nagoya, Aichi 4648601, Japan
关键词
D O I
10.1074/jbc.M111491200
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
Ypt/Rab proteins are Ras-related small GTPases that act on the intracellular membrane through the trafficking pathway, and their function depends on their localization. Approximately 25 genes encoding Ypt3/Rab11-related proteins exist in Arabidopsis, but the reason for the presence of many genes in plants remains unclear. Pea Pra2 and Pra3, members of Ypt3/Rab11, are closely related proteins. Because possible orthologs are conserved among dicots, they can be studied to determine their possible localization. Biochemical analysis revealed that these proteins were localized on distinct membranes in pea. Furthermore, using green fluorescent protein-Pra2 and green fluorescent protein-Pra3 fusion proteins, we demonstrated that these proteins are distinctively localized on the trafficking pathway in tobacco Bright Yellow 2 cells. Pra2 was predominantly localized on Golgi stacks and endosomes, which did not support the localization of Pra2 on the endoplasmic reticulum (Kang, J. G., Yun, J., Kim, D. H., Chung, K. S., Fujioka, S., Kim, J. I., Dae, H. W., Yoshida, S., Takatsuto, S., Song, P. S., and Park, C. M. (2001) Cell 105, 625-636). In contrast, Pra3 was likely to be localized on the trans-Golgi network and/or the prevacuolar compartment. We concluded that Pra2 and Pra3 proteins are distinctively localized on the trafficking pathway. This finding suggests that functional diversification takes place in the plant Ypt3/Rab11 family.
引用
收藏
页码:9183 / 9188
页数:6
相关论文
共 42 条
[1]   Cloning and subcellular location of an Arabidopsis receptor-like protein that shares common features with protein-sorting receptors of eukaryotic cells [J].
Ahmed, SU ;
BarPeled, M ;
Raikhel, NV .
PLANT PHYSIOLOGY, 1997, 114 (01) :325-336
[2]  
ALI MS, 1985, PLANT CELL PHYSIOL, V26, P1119
[3]   Analysis of the genome sequence of the flowering plant Arabidopsis thaliana [J].
Kaul, S ;
Koo, HL ;
Jenkins, J ;
Rizzo, M ;
Rooney, T ;
Tallon, LJ ;
Feldblyum, T ;
Nierman, W ;
Benito, MI ;
Lin, XY ;
Town, CD ;
Venter, JC ;
Fraser, CM ;
Tabata, S ;
Nakamura, Y ;
Kaneko, T ;
Sato, S ;
Asamizu, E ;
Kato, T ;
Kotani, H ;
Sasamoto, S ;
Ecker, JR ;
Theologis, A ;
Federspiel, NA ;
Palm, CJ ;
Osborne, BI ;
Shinn, P ;
Conway, AB ;
Vysotskaia, VS ;
Dewar, K ;
Conn, L ;
Lenz, CA ;
Kim, CJ ;
Hansen, NF ;
Liu, SX ;
Buehler, E ;
Altafi, H ;
Sakano, H ;
Dunn, P ;
Lam, B ;
Pham, PK ;
Chao, Q ;
Nguyen, M ;
Yu, GX ;
Chen, HM ;
Southwick, A ;
Lee, JM ;
Miranda, M ;
Toriumi, MJ ;
Davis, RW .
NATURE, 2000, 408 (6814) :796-815
[4]   Two GTPase isoforms, ypt31p and ypt32p, are essential for Golgi function in yeast [J].
Benli, M ;
Doring, F ;
Robinson, DG ;
Yang, XP ;
Gallwitz, D .
EMBO JOURNAL, 1996, 15 (23) :6460-6475
[5]   A genomic perspective on membrane compartment organization [J].
Bock, JB ;
Matern, HT ;
Peden, AA ;
Scheller, RH .
NATURE, 2001, 409 (6822) :839-841
[6]   Identification of new protein species among 33 different small GTP-binding proteins encoded by cDNAs from Lotos japonicus, and expression of corresponding mRNAs in developing root nodules [J].
Borg, S ;
Brandstrup, B ;
Jensen, TJ ;
Poulsen, C .
PLANT JOURNAL, 1997, 11 (02) :237-250
[7]   The role of ARF and Rab GTPases in membrane transport [J].
Chavrier, P ;
Goud, B .
CURRENT OPINION IN CELL BIOLOGY, 1999, 11 (04) :466-475
[8]   COMPARTMENTATION OF THE GOLGI-COMPLEX - BREFELDIN-A DISTINGUISHES TRANS-GOLGI CISTERNAE FROM THE TRANS-GOLGI NETWORK [J].
CHEGE, NW ;
PFEFFER, SR .
JOURNAL OF CELL BIOLOGY, 1990, 111 (03) :893-899
[9]   Characterization of hsr201 and hsr515, two tobacco genes preferentially expressed during the hypersensitive reaction provoked by phytopathogenic bacteria [J].
Czernic, P ;
Huang, HC ;
Marco, Y .
PLANT MOLECULAR BIOLOGY, 1996, 31 (02) :255-265
[10]   DIFFERENT INTRACELLULAR-LOCALIZATION OF 2 CYTOCHROME-P-450 SYSTEMS, IPOMEAMARONE 15-HYDROXYLASE AND CINNAMIC ACID 4-HYDROXYLASE, IN SWEET-POTATO ROOT-TISSUE INFECTED WITH CERATOCYSTIS-FIMBRIATA [J].
FUJITA, M ;
ASAHI, T .
PLANT AND CELL PHYSIOLOGY, 1985, 26 (03) :389-395