Cell autonomy of lin-12 function in a cell fate decision in C. elegans

Cell ◽  
1989 ◽  
Vol 57 (7) ◽  
pp. 1237-1245 ◽  
Author(s):  
Geraldine Seydoux ◽  
Iva Greenwald
2019 ◽  
Vol 29 (18) ◽  
pp. 3094-3100.e4 ◽  
Author(s):  
Michelle A. Attner ◽  
Wolfgang Keil ◽  
Justin M. Benavidez ◽  
Iva Greenwald

Development ◽  
1996 ◽  
Vol 122 (11) ◽  
pp. 3617-3626 ◽  
Author(s):  
A.P. Newman ◽  
J.G. White ◽  
P.W. Sternberg

We have undertaken electron micrographic reconstruction of the Caenorhabditis elegans hermaphrodite uterus and determined the correspondence between cells defined by their lineage history and differentiated cell types. In this organ, many cells do not move during morphogenesis and the cell lineage may function to put cells where they are needed. Differentiated uterine cell types include the toroidal ut cells that make structural epithelium, and specialized utse and uv cells that make the connection between the uterus and the vulva. A cell fate decision in which the anchor cell (AC) induces adjacent ventral uterine intermediate precursor cells to adopt the pi fate, rather than the ground state rho, has profound consequences for terminal differentiation: all pi progeny are directly involved in making the uterine-vulval connection whereas all rho progeny contribute to ut toroids or the uterine-spermathecal valve. In addition to specifying certain uterine cell fates, the AC also induces the vulva. Its multiple inductions thereby function to coordinate the connection of an internal to an external epithelium. The AC induces the pi cells and ultimately fuses with a subset of their progeny. This is an example of reciprocal cell-cell interaction that can be studied at single cell resolution. The AC is thus a transitory cell type that plays a pivotal role in organizing the morphogenesis of the uterine-vulval connection.


PLoS Genetics ◽  
2012 ◽  
Vol 8 (6) ◽  
pp. e1002732 ◽  
Author(s):  
Sudeep D. Agarwala ◽  
Hannah G. Blitzblau ◽  
Andreas Hochwagen ◽  
Gerald R. Fink

Science ◽  
2019 ◽  
Vol 366 (6461) ◽  
pp. 116-120 ◽  
Author(s):  
Nathan D. Lord ◽  
Thomas M. Norman ◽  
Ruoshi Yuan ◽  
Somenath Bakshi ◽  
Richard Losick ◽  
...  

Cell fate decision circuits must be variable enough for genetically identical cells to adopt a multitude of fates, yet ensure that these states are distinct, stably maintained, and coordinated with neighboring cells. A long-standing view is that this is achieved by regulatory networks involving self-stabilizing feedback loops that convert small differences into long-lived cell types. We combined regulatory mutants and in vivo reconstitution with theory for stochastic processes to show that the marquee features of a cell fate switch in Bacillus subtilis—discrete states, multigenerational inheritance, and timing of commitments—can instead be explained by simple stochastic competition between two constitutively produced proteins that form an inactive complex. Such antagonistic interactions are commonplace in cells and could provide powerful mechanisms for cell fate determination more broadly.


Nature ◽  
2006 ◽  
Vol 439 (7075) ◽  
pp. 502-502
Author(s):  
Alejandro Colman-Lerner ◽  
Andrew Gordon ◽  
Eduard Serra ◽  
Tina Chin ◽  
Orna Resnekov ◽  
...  

2018 ◽  
Vol 14 (4) ◽  
Author(s):  
Delphine Aymoz ◽  
Carme Solé ◽  
Jean‐Jerrold Pierre ◽  
Marta Schmitt ◽  
Eulàlia de Nadal ◽  
...  

Nature ◽  
2005 ◽  
Vol 433 (7028) ◽  
pp. 813-814 ◽  
Author(s):  
Ellen A. Robey

Nature ◽  
2005 ◽  
Vol 437 (7059) ◽  
pp. 699-706 ◽  
Author(s):  
Alejandro Colman-Lerner ◽  
Andrew Gordon ◽  
Eduard Serra ◽  
Tina Chin ◽  
Orna Resnekov ◽  
...  

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