Improvements to gene deletion in the fungal pathogen Cryptococcus neoformans:: Absence of Ku proteins increases homologous recombination, and co-transformation of independent DNA molecules allows rapid complementation of deletion phenotypes

被引:95
作者
Goins, Chelsey L.
Gerik, Kimberly J.
Lodge, Jennifer K.
机构
[1] St Louis Univ, Sch Med, Edward A Doisy Dept Biochem & Mol Biol, St Louis, MO 63104 USA
[2] St Louis Univ, Sch Med, Dept Mol Microbiol & Immunol, St Louis, MO 63104 USA
关键词
homologous recombination; non-homologous end joining; LACI; CAP59;
D O I
10.1016/j.fgb.2006.02.007
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Cryptococcus neoformans is a pathogenic fungus that is relatively amenable to molecular genetic analysis, including gene deletion. However, rates of homologous recombination can be low, so obtaining specific gene deletion transformants is challenging. We have utilized two new technologies, cku deletion strains to improve the efficiency of gene deletions in this organism, and co-transformations. The Ku70-Ku80 heterodimer is predicted to be an essential part of the non-homologous end-joining process in C neoformans. Here we show that a deletion in one or both of these proteins results in an increase in the rates of homologous recombination. Importantly, we demonstrate that after generation of a strain with a particular deletion of interest, the cku deletion can be removed by mating and segregation. We also utilize co-transformation of wild-type genes and selectable markers on separate linear DNA molecules to complement a deletion event. We show that co-transformation results in the successful restoration of wild-type phenotype, though variations in this phenotype often occur. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:531 / 544
页数:14
相关论文
共 26 条
[1]   Co-transformation with autonomous replicating and integrative plasmids in Penicillium chrysogenum is highly efficient and leads in some cases to rescue of the intact integrative plasmid [J].
Bañuelos, O ;
Naranjo, L ;
Casqueiro, J ;
Gutiérrez, S ;
Martín, JF .
FUNGAL GENETICS AND BIOLOGY, 2003, 40 (02) :83-92
[2]  
Casadevall A, 1998, CRYPTOCOCCUS NEOFORM, DOI DOI 10.1128/9781555818241
[3]   COMPLEMENTATION OF A CAPSULE-DEFICIENT MUTATION OF CRYPTOCOCCUS-NEOFORMANS RESTORES ITS VIRULENCE [J].
CHANG, YC ;
KWONCHUNG, KJ .
MOLECULAR AND CELLULAR BIOLOGY, 1994, 14 (07) :4912-4919
[4]   PIGMENT PRODUCTION BY CRYPTOCOCCUS-NEOFORMANS FROM PARA-DIPHENOLS AND ORTHO-DIPHENOLS - EFFECT OF NITROGEN-SOURCE [J].
CHASKES, S ;
TYNDALL, RL .
JOURNAL OF CLINICAL MICROBIOLOGY, 1975, 1 (06) :509-514
[5]   DNA-end-joining: from yeast to man [J].
Critchlow, SE ;
Jackson, SP .
TRENDS IN BIOCHEMICAL SCIENCES, 1998, 23 (10) :394-398
[6]   Gene disruption by biolistic transformation in serotype D strains of Cryptococcus neoformans [J].
Davidson, RC ;
Cruz, MC ;
Sia, RAL ;
Allen, B ;
Alspaugh, JA ;
Heitman, J .
FUNGAL GENETICS AND BIOLOGY, 2000, 29 (01) :38-48
[7]   A PCR-based strategy to generate integrative targeting alleles with large regions of homology [J].
Davidson, RC ;
Blankenship, JR ;
Kraus, PR ;
Berrios, MD ;
Hull, CM ;
D'Souza, C ;
Wang, P ;
Heitman, J .
MICROBIOLOGY-SGM, 2002, 148 :2607-2615
[8]  
FUJIMURA HA, 1993, BIOTECHNIQUES, V14, P538
[9]   Cell wall integrity is dependent on the PKC1 signal transduction pathway in Cryptococcus neoformans [J].
Gerik, KJ ;
Donlin, MJ ;
Soto, CE ;
Banks, AM ;
Banks, IR ;
Maligie, MA ;
Selitrennikoff, CP ;
Lodge, JK .
MOLECULAR MICROBIOLOGY, 2005, 58 (02) :393-408
[10]   Development of positive selectable markers for the fungal pathogen Cryptococcus neoformans [J].
Hua, J ;
Meyer, JD ;
Lodge, JK .
CLINICAL AND DIAGNOSTIC LABORATORY IMMUNOLOGY, 2000, 7 (01) :125-128