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Title: | Unique C-terminal region of Hap3 is required for methanol-regulated gene expression in the methylotrophic yeast Candida boidinii |
Authors: | Oda, Saori Yurimoto, Hiroya ![]() ![]() ![]() Nitta, Nobuhisa Sakai, Yasuyoshi ![]() ![]() |
Author's alias: | 小田, 沙織 由里本, 博也 新田, 暢久 阪井, 康能 |
Issue Date: | May-2016 |
Publisher: | Microbiology Society |
Journal title: | Microbiology |
Volume: | 162 |
Issue: | 5 |
Start page: | 898 |
End page: | 907 |
Abstract: | The Hap complex of the methylotrophic yeast Candida boidinii was found to be required for methanol-regulated gene expression. In this study, we performed functional characterization of CbHap3p, one of the Hap complex components in C. boidinii. Sequence alignment of Hap3 proteins revealed the presence of a unique extended C-terminal region, which is not present in Hap3p from Saccharomyces cerevisiae (ScHap3p), but is found in Hap3p proteins of methylotrophic yeasts. Deletion of the C-terminal region of CbHap3p (Δ256–292 or Δ107–237) diminished activation of methanol-regulated genes and abolished the ability to grow on methanol, but did not affect nuclear localization or DNA-binding ability. However, deletion of the N-terminal region of CbHap3p (Δ1–20) led to not only a growth defect on methanol and a decreased level of methanol-regulated gene expression, but also impaired nuclear localization and binding to methanol-regulated gene promoters. We also revealed that CbHap3p could complement the growth defect of the Schap3Δ strain on glycerol, although ScHap3p could not complement the growth defect of a Cbhap3Δ strain on methanol. We conclude that the unique C-terminal region of CbHap3p contributes to maximum activation of methanol-regulated genes, whilst the N-terminal region is required for nuclear localization and binding to DNA. |
Rights: | © Saori Oda, et al., 2016. The definitive peer reviewed, edited version of this article is published in Microbiology, volume 162, issue 5, 2016, https://doi.org/10.1099/mic.0.000275. This manuscript is under the Creative Commons Attribution 4.0 International license. |
URI: | http://hdl.handle.net/2433/266865 |
DOI(Published Version): | 10.1099/mic.0.000275 |
PubMed ID: | 26963751 |
Appears in Collections: | Journal Articles |

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