Our lab explores: (1) epigenetic mechanisms by which information in the genome is expressed in a stable and heritable fashion through cell division; (2) molecular mechanisms by which cells commit to specific fates during animal development; (3) genetic programming of cell fate decisions; (4) mechanisms by which an embryo counts the number of sex chromosomes to determine its sex; (5) mechanisms by which chromosomes adopt the correct structure to achieve faithful segregation and hence genome stability; (6) the control of recombination during the formation of sperm and eggs; (7) the control of X-chromosome-wide gene expression through the process of dosage compensation. We combine genetic, genomic, proteomic, molecular, biochemical, and cell biological approaches to study these questions in the model organism, Caenorhabditis elegans, a round worm.

Featured Science
Recent Publications
Mets, D. G., Meyer, B. J. (2009)  A Condensin Complex Regulates DSB Distribution and thus Crossover Frequency by Controlling Chromosome Structure.  Cell 139, 73-86.[PDF][Supp.PDF]
Severson, A.F., Ling, L., van Zuylen, V., Meyer, B.J. (2009)  The axial element protein HTP-3 promotes cohesin loading and meiotic axis assembly in C. elegans to implement the meiotic program of chromosome segregation.  Genes & Development 23 (15), 1763-1778. [PDF][Supp.PDF]

Jans, J. Gladden, J. M., Ralston, E. J., Pickle, C. S., Michel, A. H., Pferdehirt, R. R., Eisen, M. B., Meyer, B. J. (2009)  A condensin-like dosage compensation complex acts at a distance to control expression throughout the genome.   Genes & Development 23 (5), 602-618. [PDF][Supp.PDF]

 

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Our lab is affiliated with Howard Hughes Medical Institute and UC Berkeley. We are in the Department of Molecular and Cell Biology.

HHMI

UC Berkeley