scholarly journals Cell fate control by pioneer transcription factors

Development ◽  
2016 ◽  
Vol 143 (11) ◽  
pp. 1833-1837 ◽  
Author(s):  
Makiko Iwafuchi-Doi ◽  
Kenneth S. Zaret
2021 ◽  
Vol 12 (1) ◽  
Author(s):  
Yan Wu ◽  
Jiaqi Wu ◽  
Minghua Deng ◽  
Yihan Lin

AbstractRecent single-cell studies have revealed that yeast stress response involves transcription factors that are activated in pulses. However, it remains unclear whether and how these dynamic transcription factors temporally interact to regulate stress survival. Here we show that budding yeast cells can exploit the temporal relationship between paralogous general stress regulators, Msn2 and Msn4, during stress response. We find that individual pulses of Msn2 and Msn4 are largely redundant, and cells can enhance the expression of their shared targets by increasing their temporal divergence. Thus, functional redundancy between these two paralogs is modulated in a dynamic manner to confer fitness advantages for yeast cells, which might feed back to promote the preservation of their redundancy. This evolutionary implication is supported by evidence from Msn2/Msn4 orthologs and analyses of other transcription factor paralogs. Together, we show a cell fate control mechanism through temporal redundancy modulation in yeast, which may represent an evolutionarily important strategy for maintaining functional redundancy between gene duplicates.


2018 ◽  
Author(s):  
Amaleah Hartman ◽  
Xiao Hu ◽  
Xinyue Chen ◽  
Anna E. Eastman ◽  
Cindy Yang ◽  
...  

SUMMARYWhile Yes-associated protein (YAP) antagonizes pluripotency during early embryogenesis, it has also been shown to promote stemness of multiple stem cell types, including pluripotent stem cells. Whether cellular context underlies these distinct functions of YAP in pluripotency remains unclear. Here, we establish that depending on the specific cells in which it is expressed, YAP exhibits opposing effects on pluripotency induction from somatic cells. Specifically, YAP inhibits pluripotency induction cell-autonomously but promotes it non-cell-autonomously. For its non-cell-autonomous role, YAP alters the expression of many secreted and matricellular proteins including CYR61, which recapitulates the promotional effect when added as a recombinant protein. Thus, we define a unique YAP-driven non-cell-autonomous process that enhances pluripotency induction. Our work highlights the importance of considering the distinct contributions from heterologous cell types in deciphering the mechanism of cell fate control and calls for careful re-examination of the co-existing bystander cells in complex cultures or tissues.


Author(s):  
Leonora Buzanska ◽  
Marzena Zychowicz ◽  
Ana Ruiz ◽  
François Rossi

2010 ◽  
Vol 24 (4) ◽  
pp. 327-332 ◽  
Author(s):  
J. K. Wang ◽  
M.-C. Tsai ◽  
G. Poulin ◽  
A. S. Adler ◽  
S. Chen ◽  
...  

2004 ◽  
Vol 2 (10) ◽  
pp. 771-771
Author(s):  
Susan Jones

BMC Biology ◽  
2013 ◽  
Vol 11 (1) ◽  
pp. 73 ◽  
Author(s):  
Xi Chen ◽  
Jia Chen ◽  
Siting Gan ◽  
Huaji Guan ◽  
Yuan Zhou ◽  
...  

2005 ◽  
Vol preprint (2007) ◽  
pp. e130
Author(s):  
Alborz Mahdavi ◽  
Ryan E Davey ◽  
Patrick Bhola ◽  
Ting Yin ◽  
Peter W Zandstra

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