TY - JOUR
T1 - Efficient gene targeting in δCc.ku70 or δCc.lig4 mutants of the agaricomycete coprinopsis cinerea
AU - Nakazawa, Takehito
AU - Ando, Yuki
AU - Kitaaki, Kohei
AU - Nakahori, Kiyoshi
AU - Kamada, Takashi
N1 - Funding Information:
The work presented in this paper was supported in part by the research grant of ‘‘Elucidation of Biological Mechanisms of Photoresponse and Development of Advanced Technologies Utilizing Light” by Agriculture, Forestry and Fisheries Research Council (AFFRC), Japan and by a Grant-in-Aid for Scientific Research from the Ministry of Education, Culture, Sports, Science, and Technology of Japan and Research Fellowships of the Japan Society for the Promoting of Science (JSPS) for Young Scientists (08J00332). We thank Lorna Casselton at University of Oxford for information about literature on gene targeting in C. cinerea . We greatly appreciate Hajime Muraguchi at Akita Prefectural University for his kindly providing plasmid pBFlt. We also appreciate Shinobu Adachi for technical assistance.
PY - 2011/10
Y1 - 2011/10
N2 - Coprinopsis cinerea is a model for studies of sexual development in agaricomycetes (homobasidiomycetes). Efficient gene targeting should facilitate such studies, especially because increasing genome and transcriptome information is now available in C. cinerea. To estimate the frequency of gene disruption by homologous integration in this fungus, we tried to disrupt Cc.wc-2, which encodes a WC-2 homolog, a partner of the fungal blue-light photoreceptor, WC-1. Disruption of Cc.wc-2 did not occur when recipients (protoplasts) of the disrupting construct were prepared from asexual spores, oidia, from the wild type, 326, while it occurred when protoplasts were prepared from mycelial cells from the same strain, albeit at a low frequency (3%). Double-stranded RNA-mediated silencing of a ku70 homolog, named Cc.ku70, or the lig4 homolog Cc.lig4 more or less increased the frequency of Cc.wc-2 targeting. On the basis of these results, we disrupted Cc.ku70 using a Cc.lig4-silenced strain. We then disrupted Cc.lig4 using the Cc.ku70 disruptant. We found that the disruption of Cc.ku70 or Cc.lig4 greatly enhanced gene targeting. In addition, this study demonstrates that Cc.wc-2 is involved in blue light perception in this fungus.
AB - Coprinopsis cinerea is a model for studies of sexual development in agaricomycetes (homobasidiomycetes). Efficient gene targeting should facilitate such studies, especially because increasing genome and transcriptome information is now available in C. cinerea. To estimate the frequency of gene disruption by homologous integration in this fungus, we tried to disrupt Cc.wc-2, which encodes a WC-2 homolog, a partner of the fungal blue-light photoreceptor, WC-1. Disruption of Cc.wc-2 did not occur when recipients (protoplasts) of the disrupting construct were prepared from asexual spores, oidia, from the wild type, 326, while it occurred when protoplasts were prepared from mycelial cells from the same strain, albeit at a low frequency (3%). Double-stranded RNA-mediated silencing of a ku70 homolog, named Cc.ku70, or the lig4 homolog Cc.lig4 more or less increased the frequency of Cc.wc-2 targeting. On the basis of these results, we disrupted Cc.ku70 using a Cc.lig4-silenced strain. We then disrupted Cc.lig4 using the Cc.ku70 disruptant. We found that the disruption of Cc.ku70 or Cc.lig4 greatly enhanced gene targeting. In addition, this study demonstrates that Cc.wc-2 is involved in blue light perception in this fungus.
KW - Cc.wc-2
KW - Coprinus cinereus
KW - Gene targeting
KW - Homologous integration
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U2 - 10.1016/j.fgb.2011.06.003
DO - 10.1016/j.fgb.2011.06.003
M3 - Article
C2 - 21704178
AN - SCOPUS:80052261097
SN - 1087-1845
VL - 48
SP - 939
EP - 946
JO - Fungal Genetics and Biology
JF - Fungal Genetics and Biology
IS - 10
ER -