Inventory of the superfamily of P-type ion pumps in Arabidopsis

被引:319
作者
Axelsen, KB
Palmgren, MG
机构
[1] Royal Vet & Agr Univ, Plant Physiol & Anat Lab, Dept Plant Biol, DK-1871 Frederiksberg C, Denmark
[2] Swiss Inst Bioinformat, SwissProt Grp, CH-1211 Geneva 4, Switzerland
关键词
D O I
10.1104/pp.126.2.696
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
A total of 45 genes encoding for P-type ATPases have been identified in the complete genome sequence of Arabidopsis. Thus, this plant harbors a primary transport capability not seen in any other eukaryotic organism sequenced so far. The sequences group in all five subfamilies of P-type ATPases. The most prominent subfamilies are P-1B ATPases (heavy metal pumps; seven members), P-2A and P-2B ATPases (Ca2+ pumps; 14 in total), P-3A ATPases (plasma membrane Wi pumps; 12 members including a truncated pump, which might represent a pseudogene or an ATPase-like protein with an alternative function), and P, ATPases (12 members). P, ATPases have been implicated in aminophosholipid flipping but it is not known whether this is a direct or an indirect effect of pump activity. Despite this apparent plethora of pumps, Arabidopsis appears to be lacking Na+ pumps and secretory pathway (PMR1-like) Ca2+-ATPases. A cluster of Arabidopsis heavy metal pumps resembles bacterial Zn2+/Co2+/Cd2+/Pb2+ transporters. Two members of the cluster have extended C termini containing putative heavy metal binding motifs. The complete inventory of P-type ATPases in Arabidopsis is an important starting point for reverse genetic and physiological approaches aiming at elucidating the biological significance of these pumps.
引用
收藏
页码:696 / 706
页数:11
相关论文
共 69 条
[1]   Alteration of stimulus-specific guard cell calcium oscillations and stomatal closing in Arabidopsis det3 mutant [J].
Allen, GJ ;
Chu, SP ;
Schumacher, K ;
Shimazaki, CT ;
Vafeados, D ;
Kemper, A ;
Hawke, SD ;
Tallman, G ;
Tsien, RY ;
Harper, JF ;
Chory, J ;
Schroeder, JI .
SCIENCE, 2000, 289 (5488) :2338-2342
[2]   Salt tolerance conferred by overexpression of a vacuolar Na+/H+ antiport in Arabidopsis [J].
Apse, MP ;
Aharon, GS ;
Snedden, WA ;
Blumwald, E .
SCIENCE, 1999, 285 (5431) :1256-1258
[3]   Evolution of substrate specificities in the P-type ATPase superfamily [J].
Axelsen, KB ;
Palmgren, MG .
JOURNAL OF MOLECULAR EVOLUTION, 1998, 46 (01) :84-101
[4]   Zinc(II) tolerance in Escherichia coli K-12: evidence that the zntA gene (o732) encodes a cation transport ATPase [J].
Beard, SJ ;
Hashim, R ;
MembrilloHernandez, J ;
Hughes, MN ;
Poole, RK .
MOLECULAR MICROBIOLOGY, 1997, 25 (05) :883-891
[5]   ADAPTATIONS TO ENVIRONMENTAL STRESSES [J].
BOHNERT, HJ ;
NELSON, DE ;
JENSEN, RG .
PLANT CELL, 1995, 7 (07) :1099-1111
[6]   At-ACA8 encodes a plasma membrane-localized calcium-ATPase of Arabidopsis with a calmodulin-binding domain at the N terminus [J].
Bonza, MC ;
Morandini, P ;
Luoni, L ;
Geisler, M ;
Palmgren, MG ;
De Michelis, MI .
PLANT PHYSIOLOGY, 2000, 123 (04) :1495-1505
[7]   A gene encoding a P-type ATPase mutated in two forms of hereditary cholestasis [J].
Bull, LN ;
van Eijk, MJT ;
Pawlikowska, L ;
DeYoung, JA ;
Juijn, JA ;
Liao, M ;
Klomp, LWJ ;
Lomri, N ;
Berger, R ;
Scharschmidt, BF ;
Knisely, AS ;
Houwen, RHJ ;
Freimer, NB .
NATURE GENETICS, 1998, 18 (03) :219-224
[8]   WILSON DISEASE AND MENKES DISEASE - NEW HANDLES ON HEAVY-METAL TRANSPORT [J].
BULL, PC ;
COX, DW .
TRENDS IN GENETICS, 1994, 10 (07) :246-252
[9]   Regulation of HMG-CoA reductase degradation requires the P-type ATPase Cod1p/Spf1p [J].
Cronin, SR ;
Khoury, A ;
Ferry, DK ;
Hampton, RY .
JOURNAL OF CELL BIOLOGY, 2000, 148 (05) :915-924
[10]   Involvement of NRAMP1 from Arabidopsis thaliana in iron transport [J].
Curie, C ;
Alonso, JM ;
Le Jean, M ;
Ecker, JR ;
Briat, JF .
BIOCHEMICAL JOURNAL, 2000, 347 (pt 3) :749-755