Faculty Opinions recommendation of Asymmetric arginine dimethylation determines life span in C. elegans by regulating forkhead transcription factor DAF-16.

Author(s):  
Pankaj Kapahi
2011 ◽  
Vol 13 (5) ◽  
pp. 505-516 ◽  
Author(s):  
Yuta Takahashi ◽  
Hiroaki Daitoku ◽  
Keiko Hirota ◽  
Hiroko Tamiya ◽  
Atsuko Yokoyama ◽  
...  

Development ◽  
2000 ◽  
Vol 127 (22) ◽  
pp. 4825-4835 ◽  
Author(s):  
L. Molin ◽  
A. Mounsey ◽  
S. Aslam ◽  
P. Bauer ◽  
J. Young ◽  
...  

The Caenorhabditis elegans gene pes-1 encodes a transcription factor of the forkhead family and is expressed in specific cells of the early embryo. Despite these observations suggesting pes-1 to have an important regulatory role in embryogenesis, inactivation of pes-1 caused no apparent phenotype. This lack of phenotype is a consequence of genetic redundancy. Whereas a weak, transitory effect was observed upon disruption of just T14G12.4 (renamed fkh-2) gene function, simultaneous disruption of the activity of both fkh-2 and pes-1 resulted in a penetrant lethal phenotype. Sequence comparison suggests these two forkhead genes are not closely related and the functional association of fkh-2 and pes-1 was only explored because of the similarity of their expression patterns. Conservation of the fkh-2/pes-1 genetic redundancy between C. elegans and the related species C. briggsae was demonstrated. Interestingly the redundancy in C. briggsae is not as complete as in C. elegans and this could be explained by alterations of pes-1 specific to the C. briggsae ancestry. With overlapping function retained on an evolutionary time-scale, genetic redundancy may be extensive and expression pattern data could, as here, have a crucial role in characterization of developmental processes.


Development ◽  
2021 ◽  
Author(s):  
Karolina Mizeracka ◽  
Julia M. Rogers ◽  
Jonathan D. Rumley ◽  
Shai Shaham ◽  
Martha L. Bulyk ◽  
...  

During convergent differentiation, multiple developmental lineages produce a highly similar or identical cell type. However, few molecular players that drive convergent differentiation are known. Here, we show that the C. elegans Forkhead transcription factor UNC-130 is required in only one of three convergent lineages that produce the same glial cell type. UNC-130 acts transiently as a repressor in progenitors and newly-born terminal cells to allow the proper specification of cells related by lineage rather than by cell type or function. Specification defects correlate with UNC-130:DNA binding, and UNC-130 can be functionally replaced by its human homolog, the neural crest lineage determinant FoxD3. We propose that, in contrast to terminal selectors that activate cell-type specific transcriptional programs in terminally differentiating cells, UNC-130 acts early and specifically in one convergent lineage to produce a cell type that also arises from molecularly distinct progenitors in other lineages.


Aging ◽  
2011 ◽  
Vol 3 (11) ◽  
pp. 1098-1109 ◽  
Author(s):  
Lan Xiang ◽  
Yukiko Nakamura ◽  
Young-Mi Lim ◽  
Yasutoyo Yamasaki ◽  
Yumi Kurokawa-Nose ◽  
...  

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