` CSHLPress.com - Scientists identify novel transcriptional regulation mode
 Checkout/View Cart

Search  (type two or more letters for suggestions): Or: Advanced Search
  
  
Browse
 
Ask Us About
 
Other CSHL Web Sites
BioSupplyNet logo graphic

BioSupplyNet gives you lab protocols; tools for data retrieval, analysis, and visualization; and information about finding kits and other laboratory supplies. Read on...

CSHL Press News

Scientists identify novel mode of transcriptional regulation

08/17/2007


Muscle Mass: Scientists identify novel mode of transcriptional regulation during myogenesis

In an upcoming issue of G&D, Drs. Maria Divina Deato and Robert Tjian (HHMI, UC Berkeley) reveal that the formation of an alternative transcriptional core promoter complex directs cell-type specific differentiation duringmyogenesis. The article uncovers a whole new level of transcriptional control of terminal cell differentiation, and will be published online ahead of its September 1 print date at www.genesdev.org.

“For nearly 30 years, we have assumed that the basal transcription machinery, particularly the highly conserved TBP and TFIID complex, would beinvariant and universal for all cell types in eukaryotes. It seems that this simplistic model will need to be revised with significant implications for mechanisms controlling multi-cellular differentiation,” explains Dr.Tjian. Skeletal muscle differentiation, or myogenesis, involves a multi-step transition from muscle precursor cells (myoblasts) to myotubes thatultimately comprise the contractile myofibers of the muscle tissue. Drs. Deato and Tjian show that during myogenesis, a component of the canonicaltranscription initiation machinery – a multi-subunit transcription factor called TFIID – is disassembled and replaced with an alternative core promoter recognition complex. The researchers determined that this alternative complex contains both TAF3 and TRF3, and is required forsuccessful myogenesis.


Genes & Development is a publication of the Cold Spring Harbor Laboratory Press. The Cold Spring Harbor Laboratory is a private, non-profit, basic research and educational institution. Scientists at the Laboratory conduct groundbreaking research in cancer, neurobiology, plant molecular genetics, genomics and bioinformatics. The Laboratory is recognized internationally for its educational activities, which include an extensive program of scientific meetings and courses that attract more than 8000 scientists to the campus each year. For more information about the Cold Spring Harbor Laboratory, visit http://www.cshl.org or call the Department of Public Affairs at (516) 367-8455.

Contact:
Heather Cosel-Pieper
Genes & Development
Cold Spring Harbor Laboratory
tel. (516) 422-4018
fax (516) 422-4093



Return to CSHL Press News index
CSH Symposia Archive Our Books on the Blogosphere GrrlScientist on Experimental Heart
Photographer Timothy Archibald on My Heart vs. The Real WOrld
The hottest jobs in science, and how to land them
Adaptationomics
New Evolution Textbook Podcasts
Georgina Ferry on Max Perutz and The Secret of Life
Editor’s Select -- Free Articles From the Current Issues of our Journals
CSH Perspectives

Cold Spring Harbor Perspectives

Defining left and right in developing embryos — the view from Nobutaka Hirokawa’s laboratory.
Nobutaka Hirokawa et al.

CSH Protocols logo art

Cold Spring Harbor Protocols

Genes and Development cover

Genes & Development

Switching of the core transcription machinery during myogenesis.
Maria Divina E. Deato and Robert Tjian
Vol. 21 (17) 2137–2149.

A tDNA establishes cohesion of a neighboring silent chromatin domain.
Rudra N. Dubey and Marc R. Gartenberg
Vol. 21 (17) 2150–2160.

Gennome Research cover

Genome Research

Learning and Memory cover

Learning & Memory

Hippocampal differentiation without recognition: An fMRI analysis of the contextual cueing task.
Anthony J. Greene, William L. Gross, Catherine L. Elsinger, and Stephen M. Rao
Vol. 14 (8) 548–553.

RNA cover

RNA

Elongation factor G stabilizes the hybrid-state conformation of the 70S ribosome.
P. Clint Spiegel, Dmitri N. Ermolenko, and Harry F. Noller
Vol. 13 (9) 1473–1482.