Critical POU domain residues confer Oct4 uniqueness in somatic cell reprogramming

被引:24
|
作者
Jin, Wensong [1 ,2 ]
Wang, Lei [3 ,4 ]
Zhu, Fei [1 ]
Tan, Weiqi [2 ]
Lin, Wei [1 ]
Chen, Dahua [2 ]
Sun, Qinmiao [1 ]
Xia, Zongping [3 ,4 ]
机构
[1] Chinese Acad Sci, Inst Zool, State Key Lab Membrane Biol, Beijing 100101, Peoples R China
[2] Chinese Acad Sci, Inst Zool, State Key Lab Stem Cell & Reprod Biol, Beijing 100101, Peoples R China
[3] Zhejiang Univ, Inst Life Sci, Hangzhou 310058, Zhejiang, Peoples R China
[4] Zhejiang Univ, Innovat Ctr Cell Signaling Network, Hangzhou 310058, Zhejiang, Peoples R China
来源
SCIENTIFIC REPORTS | 2016年 / 6卷
基金
国家教育部博士点专项基金资助;
关键词
PLURIPOTENT STEM-CELLS; TRANSCRIPTION FACTOR OCT-4; SELF-RENEWAL; MOUSE; DNA; REQUIREMENTS; FIBROBLASTS; EXPRESSION; GENERATION; INTERFACE;
D O I
10.1038/srep20818
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The POU domain transcription factor Oct4 plays critical roles in self-renewal and pluripotency of embryonic stem cells (ESCs). Together with Sox2, Klf4 and c-Myc, Oct4 can reprogram any other cell types to pluripotency, in which Oct4 is the only factor that cannot be functionally replaced by other POU family members. To investigate the determinant elements of Oct4 uniqueness, we performed Ala scan on all Ser, Thr, Tyr, Lys and Arg of murine Oct4 by testing their capability in somatic cell reprogramming. We uncovered a series of residues that are important for Oct4 functionality, in which almost all of these key residues are within the POU domains making direct interaction with DNA. The Oct4 N- and C-terminal transactivation domains (TADs) are not unique and could be replaced by the Yes-associated protein (YAP) TAD domain to support reprogramming. More importantly, we uncovered two important residues that confer Oct4 uniqueness in somatic cell reprogramming. Our systematic structure-function analyses bring novel mechanistic insight into the molecular basis of how critical residues function together to confer Oct4 uniqueness among POU family for somatic cell reprogramming.
引用
收藏
页数:12
相关论文
共 50 条
  • [41] Genetic tool for fate mapping of Oct4 (Pou5f1)-expressing cells and their progeny past the pluripotency stage
    Kuzmin, Andrey A.
    Ermakova, Veronika V.
    Sinenko, Sergey A.
    Ponomartsev, Sergey V.
    Starkova, Tatiana Y.
    Skvortsova, Elena V.
    Cherepanova, Olga
    Tomilin, Alexey N.
    STEM CELL RESEARCH & THERAPY, 2019, 10 (01)
  • [42] Sodium Butyrate Facilitates Reprogramming by Derepressing OCT4 Transactivity at the Promoter of Embryonic Stem Cell-Specific miR-302/367 Cluster
    Zhang, Zhonghui
    Xiang, Di
    Wu, Wen-Shu
    CELLULAR REPROGRAMMING, 2014, 16 (02) : 130 - 139
  • [43] Enhanced OCT4 transcriptional activity substitutes for exogenous SOX2 in cellular reprogramming
    Marthaler, Adele G.
    Adachi, Kenjiro
    Tiemann, Ulf
    Wu, Guangming
    Sabour, Davood
    Velychko, Sergiy
    Kleiter, Ingo
    Schoeler, Hans R.
    Tapia, Natalia
    SCIENTIFIC REPORTS, 2016, 6
  • [44] The Nuclear Receptor Nr5a2 Can Replace Oct4 in the Reprogramming of Murine Somatic Cells to Pluripotent Cells
    Heng, Jian-Chien Dominic
    Feng, Bo
    Han, Jianyong
    Jiang, Jianming
    Kraus, Petra
    Ng, Jia-Hui
    Orlov, Yuriy L.
    Huss, Mikael
    Yang, Lin
    Lufkin, Thomas
    Lim, Bing
    Ng, Huck-Hui
    CELL STEM CELL, 2010, 6 (02) : 167 - 174
  • [45] Oct4 mediates Muller glia reprogramming and cell cycle exit during retina regeneration in zebrafish
    Sharma, Poonam
    Gupta, Shivangi
    Chaudhary, Mansi
    Mitra, Soumitra
    Chawla, Bindia
    Khursheed, Mohammad Anwar
    Ramachandran, Rajesh
    LIFE SCIENCE ALLIANCE, 2019, 2 (05)
  • [46] BMPs functionally replace Klf4 and support efficient reprogramming of mouse fibroblasts by Oct4 alone
    Chen, Jiekai
    Liu, Jing
    Yang, Jiaqi
    Chen, You
    Chen, Jing
    Ni, Su
    Song, Hong
    Zeng, Lingwen
    Ding, Ke
    Pei, Duanqing
    CELL RESEARCH, 2011, 21 (01) : 205 - 212
  • [47] Role of Oct4 in maintaining and regaining stem cell pluripotency
    Shi, Guilai
    Jin, Ying
    STEM CELL RESEARCH & THERAPY, 2010, 1
  • [48] Establishing a Cell Model for Studying the Interaction of the Pou5f1 (Oct4) Promoter with the Genetic Environment
    Kuzmin, A. A.
    Ermakova, V. V.
    Potapenko, E. V.
    Ostroverkhova, M. G.
    Guriev, N. A.
    Tomilin, A. N.
    RUSSIAN JOURNAL OF DEVELOPMENTAL BIOLOGY, 2020, 51 (06) : 410 - 415
  • [49] An Expanded Oct4 Interaction Network: Implications for Stem Cell Biology, Development, and Disease
    Pardo, Mercedes
    Lang, Benjamin
    Yu, Lu
    Prosser, Haydn
    Bradley, Allan
    Babu, M. Madan
    Choudhary, Jyoti
    CELL STEM CELL, 2010, 6 (04) : 382 - 395
  • [50] OCT4/POU5F1 is indispensable for the lineage differentiation of the inner cell mass in bovine embryos
    Simmet, Kilian
    Kurome, Mayuko
    Zakhartchenko, Valeri
    Reichenbach, Horst-Dieter
    Springer, Claudia
    Bahr, Andrea
    Blum, Helmut
    Philippou-Massier, Julia
    Wolf, Eckhard
    FASEB JOURNAL, 2022, 36 (06)