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Crystal structures of N-terminally truncated telomerase reverse transcriptase from fungi | |
2021-05-07 | |
Source Publication | NUCLEIC ACIDS RESEARCH
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ISSN | 0305-1048 |
EISSN | 1362-4962 |
Volume | 49Issue:8Pages:4768-4781 |
Status | 已发表 |
DOI | 10.1093/nar/gkab261 |
Abstract | Telomerase plays critical roles in cellular aging, in the emergence and/or development of cancer, and in the capacity for stem-cell renewal, consists of a catalytic telomerase reverse transcriptase (TERT) and a template-encoding RNA (TER). TERs from diverse organisms contain two conserved structural elements: the template-pseudoknot (T-PK) and a helical three-way junction (TWJ). Species-specific features of the structure and function of telomerase make obtaining amore in-depth understanding of the molecular mechanism of telomerase particularly important. Here, we report the first structural studies of N-terminally truncated TERTs from Candida albicans and Candida tropicalis in apo form and complexed with their respective TWJs in several conformations. We found that Candida TERT proteins perform only one round of telomere addition in the presence or absence of PK/TWJ and display standard reverse transcriptase activity. The C-terminal domain adopts at least two extreme conformations and undergoes conformational interconversion, which regulates the catalytic activity. Most importantly, we identified a conserved tertiary structural motif, called the U-motif, which interacts with the reverse transcriptase domain and is crucial for catalytic activity. Together these results shed new light on the structure and mechanics of fungal TERTs, which show common TERT characteristics, but also display species-specific features. |
URL | 查看原文 |
Indexed By | SCIE |
Language | 英语 |
WOS Research Area | Biochemistry & Molecular Biology |
WOS Subject | Biochemistry & Molecular Biology |
WOS ID | WOS:000654670600044 |
Publisher | OXFORD UNIV PRESS |
Original Document Type | Article |
Citation statistics | |
Document Type | 期刊论文 |
Identifier | https://kms.shanghaitech.edu.cn/handle/2MSLDSTB/126943 |
Collection | 生命科学与技术学院_PI研究组_孙博组 |
Co-First Author | Rety, Stephane; Chen, Wei-Fei |
Corresponding Author | Xi, Xu-Guang |
Affiliation | 1.Northwest A&F Univ, Coll Life Sci, State Key Lab Crop Stress Biol Arid Areas, Yangling 712100, Shaanxi, Peoples R China; 2.Univ Claude Bernard, Univ Lyon, ENS Lyon, CNRS UMR 5239,INSERM U1210,LBMC, 46 Allee Italie Site Jacques Monod, F-69007 Lyon, France; 3.Univ Orleans, INRA, Lab Biol Ligneux & Grandes Cultures LBLGC, USC1328, F-45067 Orleans, France; 4.CNRS, Inst Curie, UMR 144, Paris, France; 5.ShanghaiTech Univ, Sch Life Sci & Technol, Shanghai 201210, Peoples R China; 6.Chinese Acad Sci, Inst Phys, Beijing Natl Lab Condensed Matter Phys, Beijing 100190, Peoples R China; 7.Chinese Acad Sci, Inst Phys, CAS Key Lab Soft Matter Phys, Beijing 100190, Peoples R China; 8.Univ Chinese Acad Sci, Sch Phys Sci, Beijing 100049, Peoples R China; 9.Univ Paris Saclay, Inst DAlembert, Lab Biol & Pharmacol Appl LBPA, Ecole Normale Super Paris Saclay,UMR 8113,CNRS, 4 Ave Sci, F-91190 Gif Sur Yvette, France |
Recommended Citation GB/T 7714 | Zhai, Liu-Tao,Rety, Stephane,Chen, Wei-Fei,et al. Crystal structures of N-terminally truncated telomerase reverse transcriptase from fungi[J]. NUCLEIC ACIDS RESEARCH,2021,49(8):4768-4781. |
APA | Zhai, Liu-Tao.,Rety, Stephane.,Chen, Wei-Fei.,Song, Ze-Yu.,Auguin, Daniel.,...&Xi, Xu-Guang.(2021).Crystal structures of N-terminally truncated telomerase reverse transcriptase from fungi.NUCLEIC ACIDS RESEARCH,49(8),4768-4781. |
MLA | Zhai, Liu-Tao,et al."Crystal structures of N-terminally truncated telomerase reverse transcriptase from fungi".NUCLEIC ACIDS RESEARCH 49.8(2021):4768-4781. |
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