scholarly journals Cell-Type-Specific Control of Brainstem Locomotor Circuits by Basal Ganglia

Cell ◽  
2016 ◽  
Vol 164 (3) ◽  
pp. 526-537 ◽  
Author(s):  
Thomas K. Roseberry ◽  
A. Moses Lee ◽  
Arnaud L. Lalive ◽  
Linda Wilbrecht ◽  
Antonello Bonci ◽  
...  
1990 ◽  
Vol 64 (4) ◽  
pp. 1657-1666 ◽  
Author(s):  
J R Erselius ◽  
B Jostes ◽  
A K Hatzopoulos ◽  
L Mosthaf ◽  
P Gruss

1997 ◽  
Vol 16 (4) ◽  
pp. 485-492 ◽  
Author(s):  
SEUNG-JAE LEE ◽  
YOUNG YIL BAHK ◽  
DOO HEE YUN ◽  
HE-JIN LEE ◽  
YOUNG HAN LEE ◽  
...  

2010 ◽  
Vol 30 (6) ◽  
pp. 2150-2159 ◽  
Author(s):  
S. Otte ◽  
A. Hasenstaub ◽  
E. M. Callaway

Development ◽  
1999 ◽  
Vol 126 (9) ◽  
pp. 1793-1803 ◽  
Author(s):  
D.A. Lehman ◽  
B. Patterson ◽  
L.A. Johnston ◽  
T. Balzer ◽  
J.S. Britton ◽  
...  

Mitosis in most Drosophila cells is triggered by brief bursts of transcription of string (stg), a Cdc25-type phosphatase that activates the mitotic kinase, Cdk1 (Cdc2). To understand how string transcription is regulated, we analyzed the expression of string-lacZ reporter genes covering approximately 40 kb of the string locus. We also tested protein coding fragments of the string locus of 6 kb to 31.6 kb for their ability to complement loss of string function in embryos and imaginal discs. A plethora of cis-acting elements spread over >30 kb control string transcription in different cells and tissue types. Regulatory elements specific to subsets of epidermal cells, mesoderm, trachea and nurse cells were identified, but the majority of the string locus appears to be devoted to controlling cell proliferation during neurogenesis. Consistent with this, compact promotor-proximal sequences are sufficient for string function during imaginal disc growth, but additional distal elements are required for the development of neural structures in the eye, wing, leg and notum. We suggest that, during evolution, cell-type-specific control elements were acquired by a simple growth-regulated promoter as a means of coordinating cell division with developmental processes, particularly neurogenesis.


1991 ◽  
Vol 5 (11) ◽  
pp. 1624-1632 ◽  
Author(s):  
Wolfgang Doppler ◽  
Andreas Villunger ◽  
Patricia Jennewein ◽  
Karin Brduscha ◽  
Bernd Groner ◽  
...  

2019 ◽  
Author(s):  
Karolina Mizeracka ◽  
Julia M. Rogers ◽  
Jonathan D. Rumley ◽  
Shai Shaham ◽  
Martha L. Bulyk ◽  
...  

ABSTRACTDuring convergent differentiation, multiple developmental lineages produce a highly similar or identical cell type. However, the molecular players that drive convergent differentiation are not 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. 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 earlier to enable molecularly distinct progenitors to produce equivalent cell types. These findings provide evidence that convergent differentiation involves distinct transcriptional paths leading to the same cell type.


Sign in / Sign up

Export Citation Format

Share Document