Literature DB >> 26970633

Cell Fate Determination by Transcription Factors.

John B Gurdon1.   

Abstract

Transcription factors fulfill a key role in the formation and maintenance of different cell-types during development. It is known that transcription factors largely dissociate from chromosomes during mitosis. We found, previously, that mitosis is also a time when somatic nuclei can be far more easily reprogrammed after nuclear transfer than the nuclei of interphase cells. We refer to this as a mitotic advantage. Here, the rate of exchange of a transcription factor on its designated DNA-binding site is discussed. It is proposed that the Xenopus oocyte could serve as an experimental system in which the duration of binding site occupancy could be usefully analyzed. In particular, the Xenopus oocyte has several characteristics which make it possible to determine accurately the concentration and duration of transcription factor binding. It is proposed that the concentration and time are the key variables which govern the action of transcription factors when they activate genes needed for cell lineage determination.
© 2016 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Dwell time; Microinjection; Site occupation time; Transcription factors; Xenopus oocyte

Mesh:

Substances:

Year:  2016        PMID: 26970633     DOI: 10.1016/bs.ctdb.2015.10.005

Source DB:  PubMed          Journal:  Curr Top Dev Biol        ISSN: 0070-2153            Impact factor:   4.897


  7 in total

1.  Self-Reporting Transposons Enable Simultaneous Readout of Gene Expression and Transcription Factor Binding in Single Cells.

Authors:  Arnav Moudgil; Michael N Wilkinson; Xuhua Chen; June He; Alexander J Cammack; Michael J Vasek; Tomás Lagunas; Zongtai Qi; Matthew A Lalli; Chuner Guo; Samantha A Morris; Joseph D Dougherty; Robi D Mitra
Journal:  Cell       Date:  2020-07-24       Impact factor: 41.582

Review 2.  The role of NURR1 in metabolic abnormalities of Parkinson's disease.

Authors:  Murad Al-Nusaif; Yuting Yang; Song Li; Cheng Cheng; Weidong Le
Journal:  Mol Neurodegener       Date:  2022-06-27       Impact factor: 18.879

3.  Maternal pluripotency factors initiate extensive chromatin remodelling to predefine first response to inductive signals.

Authors:  George E Gentsch; Thomas Spruce; Nick D L Owens; James C Smith
Journal:  Nat Commun       Date:  2019-09-19       Impact factor: 14.919

4.  Regulation of stomatal development by stomatal lineage miRNAs.

Authors:  Jiali Zhu; Ji-Hwan Park; Seulbee Lee; Jae Ho Lee; Daehee Hwang; June M Kwak; Yun Ju Kim
Journal:  Proc Natl Acad Sci U S A       Date:  2020-03-02       Impact factor: 11.205

5.  Human transcription factors responsive to initial reprogramming predominantly undergo legitimate reprogramming during fibroblast conversion to iPSCs.

Authors:  Ricardo R Cevallos; Yvonne J K Edwards; John M Parant; Bradley K Yoder; Kejin Hu
Journal:  Sci Rep       Date:  2020-11-12       Impact factor: 4.379

6.  Runx2-Twist1 interaction coordinates cranial neural crest guidance of soft palate myogenesis.

Authors:  Xia Han; Jifan Feng; Tingwei Guo; Yong-Hwee Eddie Loh; Yuan Yuan; Thach-Vu Ho; Courtney Kyeong Cho; Jingyuan Li; Junjun Jing; Eva Janeckova; Jinzhi He; Fei Pei; Jing Bi; Brian Song; Yang Chai
Journal:  Elife       Date:  2021-01-22       Impact factor: 8.140

7.  Structurally-discovered KLF4 variants accelerate and stabilize reprogramming to pluripotency.

Authors:  Evgeniia Borisova; Ken Nishimura; Yuri An; Miho Takami; Jingyue Li; Dan Song; Mami Matsuo-Takasaki; Dorian Luijkx; Shiho Aizawa; Akihiro Kuno; Eiji Sugihara; Taka-Aki Sato; Fumiaki Yumoto; Tohru Terada; Koji Hisatake; Yohei Hayashi
Journal:  iScience       Date:  2021-12-14
  7 in total

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