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dc.contributor.authorYang, Yun Liangen_US
dc.contributor.authorWang, Chih Weien_US
dc.contributor.authorLeaw, Shiang Ningen_US
dc.contributor.authorChang, Te Pinen_US
dc.contributor.authorWang, I. Chinen_US
dc.contributor.authorChen, Chia Geunen_US
dc.contributor.authorFan, Jen Chungen_US
dc.contributor.authorTseng, Kuo Yunen_US
dc.contributor.authorHuang, Szu Hsuanen_US
dc.contributor.authorChen, Chih Yuen_US
dc.contributor.authorHsiao, Ting Yinen_US
dc.contributor.authorHsiung, Chao Agnesen_US
dc.contributor.authorChen, Chiung Tongen_US
dc.contributor.authorHsiao, Chwan Dengen_US
dc.contributor.authorLo, Hsiu Jungen_US
dc.date.accessioned2014-12-08T15:21:54Z-
dc.date.available2014-12-08T15:21:54Z-
dc.date.issued2012-03-01en_US
dc.identifier.issn1420-682Xen_US
dc.identifier.urihttp://dx.doi.org/10.1007/s00018-011-0849-5en_US
dc.identifier.urihttp://hdl.handle.net/11536/15603-
dc.description.abstractNdt80p is an important transcription modulator to various stress-response genes in Candida albicans, the most common human fungal pathogen in systemic infections. We found that Ndt80p directly regulated its target genes, such as YHB1, via the mid-sporulation element (MSE). Furthermore, the ndt80 (R432A) allele, with a reduced capability to bind MSE, failed to complement the defects caused by null mutations of NDT80. Thus, the R432 residue in the Ndt80p DNA-binding domain is involved in all tested functions, including cell separation, drug resistance, nitric oxide inactivation, germ tube formation, hyphal growth, and virulence. Hence, the importance of the R432 residue suggests a novel approach for designing new antifungal drugs by blocking the interaction between Ndt80p and its targets.en_US
dc.language.isoen_USen_US
dc.subjectCandida albicansen_US
dc.subjectNdt80en_US
dc.subjectProtein-DNA interactionen_US
dc.subjectMSEen_US
dc.subjectBinding assayen_US
dc.titleR432 is a key residue for the multiple functions of Ndt80p in Candida albicansen_US
dc.typeArticleen_US
dc.identifier.doi10.1007/s00018-011-0849-5en_US
dc.identifier.journalCELLULAR AND MOLECULAR LIFE SCIENCESen_US
dc.citation.volume69en_US
dc.citation.issue6en_US
dc.citation.spage1011en_US
dc.citation.epage1023en_US
dc.contributor.department生物科技學系zh_TW
dc.contributor.department分子醫學與生物工程研究所zh_TW
dc.contributor.departmentDepartment of Biological Science and Technologyen_US
dc.contributor.departmentInstitute of Molecular Medicine and Bioengineeringen_US
dc.identifier.wosnumberWOS:000300737200011-
dc.citation.woscount2-
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