Robust gut-specific gene expression in transgenic Aedes aegypti mosquitoes

被引:116
作者
Moreira, LA
Edwards, MJ
Adhami, F
Jasinskiene, N
James, AA
Jacobs-Lorena, M
机构
[1] Case Western Reserve Univ, Sch Med, Dept Genet, Cleveland, OH 44106 USA
[2] Ohio Wesleyan Univ, Dept Zool, Delaware, OH 43015 USA
[3] Univ Calif Irvine, Dept Mol Biol & Biochem, Irvine, CA 92697 USA
关键词
malaria; Hermes; mariner; promoter function;
D O I
10.1073/pnas.97.20.10895
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Genetic modification of the vectorial capacity of mosquito vectors of human disease requires promoters capable of driving gene expression with appropriate tissue and stage specificity. We report on the characterization in transgenic Aedes aegypti of two mosquito gut-specific promoters. A 1.4-kb DNA fragment adjacent to the 5' end of the coding region of the Ae. aegypti carboxypeptidase (AeCP) gene and a corresponding 3.4-kb DNA fragment at the 5' end of the Anopheles gambiae carboxypeptidase (AgCP) gene were linked to a firefly luciferase reporter gene and introduced into the Ae. aegypti germ line by using Hermes and mariner (Mos1) transposons. Six independent transgenic lines were obtained with the AeCP construct and one with the AgCP construct. Luciferase mRNA and protein were abundantly expressed in the guts of transgenic mosquitoes in four of the six AeCP lines and in the AgCP line. Expression of the reporter gene was gut-specific and reached peak levels at about 24 h post-blood ingestion. The AeCP and AgCP promoters can be used to drive the expression of genes that hinder parasite development in the mosquito gut.
引用
收藏
页码:10895 / 10898
页数:4
相关论文
共 20 条
[1]   CDNA AND DEDUCED AMINO-ACID-SEQUENCE OF A BLOOD MEAL-INDUCED TRYPSIN FROM THE MOSQUITO, AEDES-AEGYPTI [J].
BARILLASMURY, C ;
GRAF, R ;
HAGEDORN, HH ;
WELLS, MA .
INSECT BIOCHEMISTRY, 1991, 21 (08) :825-831
[2]  
Beard C.B., 1993, Insect Molecular Biology, V2, P103, DOI 10.1111/j.1365-2583.1993.tb00131.x
[3]   Stable germline transformation of the malaria mosquito Anopheles stephensi [J].
Catteruccia, F ;
Nolan, T ;
Loukeris, TG ;
Blass, C ;
Savakis, C ;
Kafatos, FC ;
Crisanti, A .
NATURE, 2000, 405 (6789) :959-962
[4]   Mariner transposition and transformation of the yellow fever mosquito, Aedes aegypti [J].
Coates, CJ ;
Jasinskiene, N ;
Miyashiro, L ;
James, AA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (07) :3748-3751
[5]   Promoter-directed expression of recombinant fire-fly luciferase in the salivary glands of Hermes-transformed Aedes aegypti [J].
Coates, CJ ;
Jasinskiene, N ;
Pott, GB ;
James, AA .
GENE, 1999, 226 (02) :317-325
[6]   Rapid induction by a blood meal of a carboxypeptidase gene in the gut of the mosquito Anopheles gambiae [J].
Edwards, MJ ;
Lemos, FJA ;
Donnelly-Doman, M ;
Jacobs-Lorena, M .
INSECT BIOCHEMISTRY AND MOLECULAR BIOLOGY, 1997, 27 (12) :1063-1072
[7]   Characterization of a carboxypeptidase A gene from the mosquito, Aedes aegypti [J].
Edwards, MJ ;
Moskalyk, LA ;
Donelly-Doman, M ;
Vlaskova, M ;
Noriega, FG ;
Walker, VK ;
Jacobs-Lorena, M .
INSECT MOLECULAR BIOLOGY, 2000, 9 (01) :33-38
[8]   DEVELOPMENTAL SPECIFICITY OF A BIDIRECTIONAL MOTH CHORION PROMOTER IN TRANSGENIC DROSOPHILA [J].
FENERJIAN, MG ;
KAFATOS, FC .
DEVELOPMENTAL BIOLOGY, 1994, 161 (01) :37-47
[9]   Stable transformation of the yellow fever mosquito, Aedes aegypti, with the Hermes element from the housefly [J].
Jasinskiene, N ;
Coates, CJ ;
Benedict, MQ ;
Cornel, AJ ;
Rafferty, CS ;
James, AA ;
Collins, FH .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (07) :3743-3747
[10]   cDNA cloning and pattern of expression of an adult, female-specific chymotrypsin from Aedes aegypti midgut [J].
Jiang, QJ ;
Hall, M ;
Noriega, FG ;
Wells, M .
INSECT BIOCHEMISTRY AND MOLECULAR BIOLOGY, 1997, 27 (04) :283-289