A homologue of N-ethylmaleimide-sensitive factor in the malaria parasite Plasmodium falciparum is exported and localized in vesicular structures in the cytoplasm of infected erythrocytes in the brefeldin A-sensitive pathway

被引:65
作者
Hayashi, M
Taniguchi, S
Ishizuka, Y
Kim, HS
Wataya, Y
Yamamoto, A
Moriyama, Y [1 ]
机构
[1] Okayama Univ, Fac Pharmaceut Sci, Dept Biochem, Okayama 7008530, Japan
[2] Okayama Univ, Fac Pharmaceut Sci, Dept Med Informat, Okayama 7008530, Japan
[3] Kansai Med Univ, Dept Physiol, Osaka 5708506, Japan
关键词
D O I
10.1074/jbc.M011709200
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
N-Ethylmaleimide-sensitive factor (NSF) and its homologues play a central role in vesicular trafficking in eukaryotic cells. We have identified a NSF homologue in Plasmodium falciparum (PfNSF), The reported PfNSF gene sequence (GenBank(TM) accession number CAB10575) indicated that PfNSF comprises 783 amino acids with a calculated molecular weight of 89,133, The overall identities of its gene and amino acid sequences with those of rat NSF are 50.9 and 48.8%, respectively. Reverse transcription-polymerase chain reaction analysis and Northern blotting with total P, falciparum RNA indicated expression of the PfNSF gene. Polyclonal. antibodies against a conserved region of NSF specifically recognized an 89-kDa polypeptide in the parasite cells. After homogenization of the parasite cells, similar to 90% of an 89-kDa polypeptide is associated with particulate fraction, suggesting membrane-bound nature of PfNSF. PfNSF was present within both the parasite cells and the vesicular structure outside of the parasite cells, The export of PfNSF outside of the parasite cells appears to occur at the early trophozoite stage and to terminate at the merozoite stage. The export of PfNSF is inhibited by brefeldin A, with 9 muM causing 50% inhibition. Immuno-electromicroscopy indicated that intracellular PfNSF was associated with organelles such as food vacuoles and that extracellular PfNSF was associated with vesicular structures in the erythrocyte cytoplasm, These results indicate that PfNSF expressed in the malaria parasite is exported to the extracellular space and then localized in intraerythrocytic vesicles in a brefeldin A-sensitive manner. It is suggested that a vesicular transport mechanism is involved in protein export targeted to erythrocyte membranes during intraerythrocytic development of the malaria parasite.
引用
收藏
页码:15249 / 15255
页数:7
相关论文
共 46 条
[1]   MEMBRANE-ASSOCIATED ELECTRON-DENSE MATERIAL OF THE ASEXUAL STAGES OF PLASMODIUM-FALCIPARUM - EVIDENCE FOR MOVEMENT FROM THE INTRACELLULAR PARASITE TO THE ERYTHROCYTE-MEMBRANE [J].
AIKAWA, M ;
UNI, Y ;
ANDRUTIS, AT ;
HOWARD, RJ .
AMERICAN JOURNAL OF TROPICAL MEDICINE AND HYGIENE, 1986, 35 (01) :30-36
[2]   A homologue of Sar1p localises to a novel trafficking pathway in malaria-infected erythrocytes [J].
Albano, FR ;
Berman, A ;
La Greca, N ;
Hibbs, AR ;
Wickham, M ;
Foley, M ;
Tilley, L .
EUROPEAN JOURNAL OF CELL BIOLOGY, 1999, 78 (07) :453-462
[3]   THE MOLECULAR MACHINERY FOR SECRETION IS CONSERVED FROM YEAST TO NEURONS [J].
BENNETT, MK ;
SCHELLER, RH .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (07) :2559-2563
[4]   BREFELDIN-A INHIBITS TRANSPORT OF THE GLYCOPHORIN-BINDING PROTEIN FROM PLASMODIUM-FALCIPARUM INTO THE HOST ERYTHROCYTE [J].
BENTING, J ;
MATTEI, D ;
LINGELBACH, K .
BIOCHEMICAL JOURNAL, 1994, 300 :821-826
[5]   The complete nucleotide sequence of chromosome 3 of Plasmodium falciparum [J].
Bowman, S ;
Lawson, D ;
Basham, D ;
Brown, D ;
Chillingworth, T ;
Churcher, CM ;
Craig, A ;
Davies, RM ;
Devlin, K ;
Feltwell, T ;
Gentles, S ;
Gwilliam, R ;
Hamlin, N ;
Harris, D ;
Holroyd, S ;
Hornsby, T ;
Horrocks, P ;
Jagels, K ;
Jassal, B ;
Kyes, S ;
McLean, J ;
Moule, S ;
Mungall, K ;
Murphy, L ;
Oliver, K ;
Quail, MA ;
Rajandream, MA ;
Rutter, S ;
Skelton, J ;
Squares, R ;
Squares, S ;
Sulston, JE ;
Whitehead, S ;
Woodward, JR ;
Newbold, C ;
Barrell, BG .
NATURE, 1999, 400 (6744) :532-538
[6]   SILVER ENHANCEMENT OF GOLD ANTIBODY PROBES IN PREEMBEDDING ELECTRON-MICROSCOPIC IMMUNOCYTOCHEMISTRY [J].
BURRY, RW ;
VANDRE, DD ;
HAYES, DM .
JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY, 1992, 40 (12) :1849-1856
[7]   Brefeldin A: The advantage of being uncompetitive [J].
Chardin, P ;
McCormick, F .
CELL, 1999, 97 (02) :153-155
[8]   Constitutive calcium-independent release of Toxoplasma gondii dense granules occurs through the NSF/SNAP/SNARE/Rab machinery [J].
Chaturvedi, S ;
Qi, HL ;
Coleman, D ;
Rodriguez, A ;
Hanson, PI ;
Striepen, B ;
Roos, DS ;
Joiner, KA .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (04) :2424-2431
[9]   BREFELDIN-A INHIBITS PROTEIN SECRETION AND PARASITE MATURATION IN THE RING STAGE OF PLASMODIUM-FALCIPARUM [J].
CRARY, JL ;
HALDAR, K .
MOLECULAR AND BIOCHEMICAL PARASITOLOGY, 1992, 53 (1-2) :185-192
[10]   BIOSYNTHESIS, EXPORT AND PROCESSING OF A 45 KDA PROTEIN DETECTED IN MEMBRANE CLEFTS OF ERYTHROCYTES INFECTED WITH PLASMODIUM-FALCIPARUM [J].
DAS, A ;
ELMENDORF, HG ;
LI, WI ;
HALDAR, K .
BIOCHEMICAL JOURNAL, 1994, 302 :487-496