Schistosoma mansoni:: Germ-line transformation approaches and actin-promoter analysis

被引:27
作者
Beckmann, Svenja
Wippersteg, Volker
El-Bahay, Akram
Hirzmann, Joerg
Oliveira, Guilherme
Grevelding, Christoph G.
机构
[1] Univ Giessen, Inst Parasitol, D-35392 Giessen, Germany
[2] Univ Dusseldorf, Inst Genet, D-40225 Dusseldorf, Germany
[3] Ctr Pesquisas Rene Rachou Fiocruz, BR-30190002 Belo Horizonte, MG, Brazil
关键词
Schistosoma mansoni; germ-line transformation; actin promoter region; transcription factor; CNA; calcineurin A; ER60; cysteine protease ER60; GFP; green fluorescent protein; HSP70; heat-shock protein 70; RT-PCR; reverse transcriptase polymerase chain reaction; SmAct1; Schistosoma mansoni actin gene 1; SmCF and SmCB2; S. mansoni cathepsins; TF; UT; untranslated region;
D O I
10.1016/j.exppara.2007.04.007
中图分类号
R38 [医学寄生虫学]; Q [生物科学];
学科分类号
07 ; 0710 ; 09 ; 100103 ;
摘要
Towards germ-line transformation miracidia were biolistically transformed with GFP reporter gene constructs and successfully reintroduced into the schistosome cycle. By PCR and confocal microscopy the presence and the expression of GFP were confirmed in cercariae or adults of the F-0 and F-1 generations. This indicated the presence of the constructs in the germ-line, although no evidence for genome integration was obtained. About 3 kb of 5' upstream sequences of the actin gene SmActl were identified by ill silico analyses, and different fragments up to 1.5 kb subcloned for GFP-vector construction. A 445 bp fragment was sufficient for transcription initiation in larvae or adults as confirmed by confocal microscopy. An actin gene characteristic assembly of TATA, CArG, and CAAT boxes has been identified, which seems to be functionally conserved between vertebrates and invertebrates. However, a vertebrate-specific intron containing an additional regulatory CArG box was not found indicating that the regulation of SmActl transcription depends exclusively on its promoter region. (C) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:292 / 303
页数:12
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