Molecular cloning of cDNAs for two pro-phenol oxidase subunits from the Malaria vector, Anopheles gambiae

被引:49
作者
Jiang, HB [1 ]
Wang, Y [1 ]
Korochkina, SE [1 ]
Benes, H [1 ]
Kanost, MR [1 ]
机构
[1] UNIV ARKANSAS MED SCI,DEPT BIOCHEM & MOL BIOL,LITTLE ROCK,AR 72205
关键词
mosquito; hemolymph; encapsulation; antibody;
D O I
10.1016/S0965-1748(97)00045-3
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
Phenol oxidase exists in insect hemolymph as a zymogen, pro-phenol oxidase (pro-PO), which is activated by specific proteolysis in response to infection or wounding, Phenol oxidase catalyses the synthesis of quinones that polymerize to form melanin deposits, which encapsulate parasites and help to seal wounds, Antibodies to pro-PO from Manduca sexta bound to 76, 72, and 71 kDa polypeptide bands from hemolymph of Anopheles gambiae larvae, This antiserum was used to screen a cDNA library from A, gambiae fourth-instar larvae, Pub-length clones were isolated for two different pro-POs, designated A, gambiae proPO-p1 and proPO-p2, which are 67% identical in nucleotide sequence and 66% identical in deduced amino acid sequence, The A, gambiae pro-PO sequences are more similar to pro-PO from Drosophila melanogaster than to lepidopteran or crustacean pro-PO sequences in the GenBank database. Like the other arthropod pro-POs, the A, gambiae pro-PO sequences lack a signal peptide and have two conserved regions predicted to bind two copper atoms ire the active site of the enzyme, The availability of these pro-PO cDNAs should be useful in examining the biochemical differences between A, gambiae strains that are refractory or susceptible to Plasmodium infection, and differ in their ability to encapsulate the parasites, (C) 1997 Elsevier Science Ltd.
引用
收藏
页码:693 / 699
页数:7
相关论文
共 24 条
[1]  
Ashida M., 1990, P239
[2]   STUDIES ON PROPHENOLOXIDASE ACTIVATION IN THE MOSQUITO AEDES-AEGYPTI L [J].
ASHIDA, M ;
KINOSHITA, K ;
BREY, PT .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1990, 188 (03) :507-515
[3]   CDNA CLONING OF PROPHENOLOXIDASE FROM THE FRESH-WATER CRAYFISH PACIFASTACUS-LENIUSCULUS AND ITS ACTIVATION [J].
ASPAN, A ;
HUANG, TS ;
CERENIUS, L ;
SODERHALL, K .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (04) :939-943
[4]   Immune factor Gambif1, a new rel family member from the human malaria vector, Anopheles gambiae [J].
BarillasMury, C ;
Charlesworth, A ;
Gross, I ;
Richman, A ;
Hoffmann, JA ;
Kafatos, FC .
EMBO JOURNAL, 1996, 15 (17) :4691-4701
[5]   TYROSINASE-TYPE PROPHENOLOXIDASE DISTRIBUTION IN THE ALIMENTARY CANAL OF STRAINS OF ANOPHELES-GAMBIAE REFRACTORY AND SUSCEPTIBLE TO PLASMODIUM INFECTION [J].
BREY, PT ;
AHMED, A ;
LEE, WJ ;
ASHIDA, M ;
LEHANE, MJ .
EXPERIMENTAL PARASITOLOGY, 1995, 80 (04) :654-664
[6]   PARTIAL-PURIFICATION OF PLASMA PHENOLOXIDASE OF THE YELLOW-FEVER MOSQUITO AEDES-AEGYPTI L (DIPTERA, CULICIDAE) [J].
BURKS, CS ;
FUCHS, MS .
COMPARATIVE BIOCHEMISTRY AND PHYSIOLOGY B-BIOCHEMISTRY & MOLECULAR BIOLOGY, 1995, 110 (03) :641-647
[7]   Activation of prophenoloxidase A(1) by an activating enzyme in Drosophila melanogaster [J].
Chosa, N ;
Fukumitsu, T ;
Fujimoto, K ;
Ohnishi, E .
INSECT BIOCHEMISTRY AND MOLECULAR BIOLOGY, 1997, 27 (01) :61-68
[8]   GENETIC SELECTION OF A PLASMODIUM-REFRACTORY STRAIN OF THE MALARIA VECTOR ANOPHELES-GAMBIAE [J].
COLLINS, FH ;
SAKAI, RK ;
VERNICK, KD ;
PASKEWITZ, S ;
SEELEY, DC ;
MILLER, LH ;
COLLINS, WE ;
CAMPBELL, CC ;
GWADZ, RW .
SCIENCE, 1986, 234 (4776) :607-610
[9]   NUCLEOTIDE-SEQUENCE OF THE CDNA-ENCODING THE PROENZYME OF PHENOL OXIDASE A(1) OF DROSOPHILA-MELANOGASTER [J].
FUJIMOTO, K ;
OKINO, N ;
KAWABATA, S ;
IWANAGA, S ;
OHNISHI, E .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (17) :7769-7773
[10]   PROENZYME OF MANDUCA-SEXTA PHENOL OXIDASE - PURIFICATION, ACTIVATION, SUBSTRATE-SPECIFICITY OF THE ACTIVE ENZYME, AND MOLECULAR-CLONING [J].
HALL, M ;
SCOTT, T ;
SUGUMARAN, M ;
SODERHALL, K ;
LAW, JH .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (17) :7764-7768