Palace LogoHaagLab Wordle



http://www.umd.edu


PI:  Eric S. Haag

Associate Professor

Eric at the scope

Telephone: (301) 405-8534 
Office:  Biology/Psychology Room 0256 
Lab:  Biology/Psychology Room 0245
Email: ehaag@umd.edu






The Haag Lab, April, 2012
  
                                                                      

Haag Lab, 2012

We are (L to R): Qinwen Liu, Joe Ross, Eric Haag, Cristel Thomas, Gavin Woodruff, (not shown: Becca Matteson)
 

Haag Lab People


C. briggsae wild-type XO male

briggsae hermaphrodite

     C. briggsae hermaphrodite (above) and male (left)


Research Interests

        The Haag laboratory studies the developmental genetics of evolutionary change in animals.  Of particular interest to us are reproductive adaptations whose evolution required major developmental novelties.  Currently we focus on the evolution of self-fertile hermaphroditism in nematodes.  We use the model nematode Caenorhabditis elegans as a starting point, which confers several advantages.  First, sister species of C. elegans have different reproductive modes that are based on differences in sex determination in a single tissue--the germ line.  Second, C. elegans sex determination has been subjected to intense genetic, molecular, and biochemical investigation, which provides a wealth of potential mechanisms for investigation.  Third, many of the tools available to C. elegans researchers are applicable to its relatives as well, such as classical genetics, RNA interference-mediated reverse genetics, and even complete genome sequence. 

       We seek to identify the molecular and genetic mechanisms that distinguish the sex determination of androdioecious (hermaphrodite/male) species from that of gonochoristic (male/female) species of worms.  We also use independently evolved hermaphrodites as a laboratory to explore convergent evolution.  In addition, we are interested in the evolutionary forces that drive the rapid evolution of sex determination even in the absence of overt phenotypic change, and the molecular and genomic responses to these forces. 

Work in the lab currently includes the following projects: 

  • classical and reverse genetic analysis of sex determination in other Caenorhabditis species, especially C. briggsae
  • evolutionary dynamics of germline RNA-binding proteins
  • basic and comparative characterization of key proteins of the nematode sex determination pathway
  • genome-level consequences of mating system evolution in Caenorhabditis species
  • interspecies hybrid genetics

     Feel free to contact Eric if you are interested in participating in this work.  Our lab (a.k.a. The Palace of Worm Sex) is on the ground floor of the Biology/Psychology Building.

Cb-fem-3(nm63) mutant 









At left,  a self-fertile  XX C. briggsae
fem-3(nm63)
deletion mutant.  This
phenotype (or lack therof)
differs
from
the self-sterility seen in the 
equivalent
C. elegans fem-3 mutant.
(see Hill et al. 2006)








Recent Publications:

Hill, RC, Carvalho, C, Salogiannis, J, Schlager, B, Pilgrim, D, and Haag, ES (2006)  Genetic flexibility in the convergent evolution of hermaphroditism in Caenorhabditis nematodes. Developmental Cell 10: 531-38  PDF  Suppl. Mats.

Haag, ES (2007)  Compensatory vs. pseudocompensatory evolution in molecular and developmental interactions.  Genetica 129: 45-55.    PDF

Haag, ES, Chamberlin, H, Coghlan, A, Fitch, DHA, Peters, AD, and Schulenburg, H (2007)  Caenorhabditis evolution: if they all look alike, you aren't looking hard enough.  Trends in Genetics 23: 101-04.  PDF

Kelleher, DF, de Carvalho, CE, Doty AV, Layton M, Cheng AT, Mathies LD, Pilgrim D, Haag ES (2008)  Comparative genetics of sex determination: Masculinizing mutations in Caenorhabditis briggsae. Genetics 178: 1415-29.  PDF   Suppl. Mats.

Barriere, A, Yang, S-P, Pekarek, E, Thomas, CG, Haag, ES, and Ruvinsky, I (2009)  Detecting heterozygosity in shotgun genome assemblies: Lessons from obligately outcrossing nematodes.  Genome Research 19: 470-480. PDF

Haag, E.S. (2009) Caenorhabditis nematodes as a model for the adaptive evolution of germ cells.  Chpt. 3 in Current Topics in Developmental Biology, 86: 43-66 (W. Jeffery, ed.) PDF

Hill, RC and Haag, ES (2009)  A sensitized genetic background reveals evolution near the terminus of the Caenorhabditis germline sex determination pathway.  Evolution & Development 11: 333-342  PDF

Hill & Haag cover photo    

Koboldt, DC, Staisch, J, Thillainathan, B, Haines, K, Baird, SE, Chamberlin, HM, Haag, ES, Miller, RD, and Gupta, BP (2010) A toolkit for rapid gene mapping in the nematode Caenorhabditis briggsae. BMC Genomics 11: 236. PDF

Woodruff, G.C., Eke, O., Baird, S.E., Félix, M.A., and Haag, E.S. (2010). Insights into species divergence and the evolution of hermaphroditism from fertile interspecies hybrids of Caenorhabditis nematodes. Genetics 186: 997-1012. PDF

Ross, J.A., Koboldt, D.C., Staisch, J.E., Chamberlin, H.M., Gupta, B.P., Miller, R.D., Baird, S.E., and Haag, E.S.* (2011). Caenorhabditis briggsae recombinant inbred line genotypes reveal inter-strain incompatibilities and the evolution of recombination. PLoS Genetics  7: e1002174 PDF

Haag, E.S. and Lenski, R.E. (2011) L’enfant terrible at 30:  the maturation of evolutionary developmental biology.  Development  138: 2633-38. PDF

Beadell, A.V., Liu, Q., Johnson, D.M., and Haag, E.S. (2011) Independent recruitments of a translational regulator in the evolution of self-fertile nematodes.  Proc. Natl. Acad. Sci USA 108: 19672-27 PDF

Liu, Q., Stumpf, C., Thomas, C.G., Wickens, M., and Haag E.S. (2012) Context-dependent function of a conserved translational regulatory module.  Development 139: 1509-21.PDF

Thomas, C.G., Woodruff, G.C., and Haag, E.S. (2012) Causes and consequences of the evolution of reproductive mode in Caenorhabditis nematodes. Trends in Genetics 28: 213-220.

Thomas, C.G., Li, R., Smith, H.E., Woodruff, G.C., Oliver, B., and Haag, E.S. (2012).  Simplification and desexualization of gene expression in self-fertile nematodes. Current Biology 22: 2167-2172.


 


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Research in the Haag Lab has been supported by grants from NIGMS and NSF

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