Department of Molecular and Cellular Biology, College of Biological Sciences
Meiosis and checkpoint function in the C. elegans germ line
Germ cells are specialized cells that undergo mitotic proliferation followed by meiosis and cellular differentiation to generate haploid gametes for sexual reproduction. We are investigating several aspects of germ line biology using the nematode, Caenorhabditis elegans and related nematodes. The C. elegans germ line is particularly amenable to these studies due to its unique structural organization, the molecular genetics of the system, and the high degree of conservation with genes and pathways in humans. We are currently investigating 1) how meiosis differs in males and females; 2) how unpaired sex chromosomes of the heterogametic sex repair double strand breaks and are hidden from the checkpoint machinery; and 3) how different checkpoint pathways interact to ensure the faithful transmission of the genome.
Grad Group Affiliations
- Biochemistry, Molecular, Cellular and Developmental Biology
- Integrative Genetics and Genomics
Specialties / Focus
- Cell Biology
- Cell Division and the Cytoskeleton
- Chromosome Biology
- Chromosome Dynamics and Nuclear Function
- DNA Repair
- Molecular Genetics
- Reproductive Biology
- BIS 101 Genetics, Variable
- BCB 210 Molecular Genetics and Genomics, Fall
- MCB 160L Genetics Lab, Variable
- MCB 164 Adv Eukaryotic Genetics, Spring
- MCB 10 Introduction to Human Heredity
- Engebrecht Lab http://jengebre.faculty.ucdavis.edu/
- Foxy Robinson (undergraduate)
- Alison Deshong (graduate student)
- Michelle Leung (undergraduate)
Honors and Awards
- 2012 BMCDB Award for Excellence in Teaching
- 2014 Chancellor’s Award for Excellence in Mentoring Undergraduate Research
- 2017 ADVANCE SCHOLAR AWARD
- Genetics Society of America
- The American Society for Cell Bioloy
- GENA (geneticist-educator network association)
- 1981 BS Microbiology University of Washington
- 1986 PhD Marine Biology Scripps Institution of Oceanography
Lawrence, K., E. C. Tapley, V. E. Cruz, Q. Li, K. Aung, K. C. Hart, T. U. Schwartz, D. A. Starr and J. Engebrecht (2016) LINC complexes promote homologous recombination in part through inhibition of non-homologous end joining. J Cell Biol 215, 801-822.
Van, M. V., B. J. Larson and J. Engebrecht (2016) To break or not to break: sex chromosome hemizygosity during meiosis in Caenorhabditis. Genetics 204, 999-1013.
Larson, B. J., M. V. Van, T. Nakayama and J. Engebrecht (2016) Plasticity in the meiotic epigenetic landscape of sex chromosomes in Caenorhabditis species. Genetics 203, 1641-1658.
Lawrence, K. S., T. Chau and J. Engebrecht (2015) DNA damage response and spindle assembly checkpoint function throughout the cell cycle to ensure genomic integrity. PLoS Genet.11(4):e1005150. doi: 10.1371/journal.pgen.1005150.
Checchi, P., K. Lawrence, M. Van, B. Larson and J. Engebrecht (2014) Pseudosynapsis and decreased stringency of meiotic repair pathway choice on the hemizygous sex chromosome of Caenorhabditis elegans males. Genetics 197, 543-560
Lawrence, K. S., and J. Engebrecht (2012). Slowing replication in preparation for reduction. PLoS Genetics 8(5):e1002715.
Checchi, P. and J. Engebrecht (2011). Caenorhabditis elegans Histone Methyltransferase MET-2 Shields the Male X Chromosome from Checkpoint Machinery and Mediates Meiotic Sex Chromosome Inactivation. PlosGenetics 7(9): e1002267.
Checchi, P. and J. Engebrecht (2011). Heteromorphic sex chromosomes: Navigating meiosis without a homologous partner. Mol Reprod Dev 78, 623-632.
Jaramillo-Lambert A., Y. Harigaya, J. Vitt, A. Villeneuve, J. Engebrecht (2010). Meiotic errors activate checkpoints that improve gamete quality without triggering apoptosis in male germ cells. Curr Biol. 20, 2078-2089. Comment in Curr Biol. 20:R1014-1016.
Jaramillo-Lambert, A., and J. Engebrecht (2010) A single unpaired and transcriptionally silenced X Chromosome locally precludes checkpoint signaling in the Caenorhabditis elegans germ line. Genetics (Epub ahead of print).
Mendonsa, R. and J. Engebrecht (2009). Phosphatidylinositol-4,5-bisphosphate and phospholipase D-generated phosphatidic acid specify SNARE-mediated vesicle fusion for prospore membrane formation. Eukaryot. Cell 8, 1094-1105.
Mendonsa, R. and J. Engebrecht (2009). Phospholipase D function in Saccharomyces cerevisiae. Biochim. Biophys. Acta 1791, 970-974.
Morishita, M. and J. Engebrecht (2008). Sorting signals within the Saccharomyces cerevisaie sporulation-specific dityrosine transporter, Dtr1p, C terminus promote Golgi-to-prospore membrane transport. Eukaryot. Cell 7, 1674-1684.
Jaramillo-Lambert, A., M. Elefson, A. Villeneuve, and J. Engebrecht (2007). Differential timing of S phases, X chromosome replication and meiotic progression in the C. elegans germline. Dev. Biol. 308,206-221.
Smolikov, S., A. Eizinger, K. Schild-Prufert, A. Hurlburt, K. McDonald, J. Engebrecht, A. Villeneuve, and M. Colaiacovo (2007). SYP-3 restricts synaptonemal complex assembly to bridge paired chromosome axes during meiosis in C. elegans. Genetics 176:2015-2025.
Nakanishi, H., M. Morishita, C. E. Schwartz, A. Coluccio, J. Engebrecht and A. M. Neiman (2006). Phospholipase D and the SNARE, Sso1p, are necessary for vesicle fusion during sporulation in yeast. J. Cell Sci. 119, 1406-1415.
Connolly, J., and J. Engebrecht (2006). The Arf-GAP Gcs1p is essential for sporulation and regulates the phospholipase D, Spo14p. Eukaryot. Cell. 5, 112-124.
Morishita M., and J. Engebrecht (2005). End3p-mediated endocytosis is required for spore wall formation in Saccharomyces cerevisiae. Genetics 170, 1561-1574.
Morishita, M., and J. Engebrecht (2005) Phospholipases and cell signaling in yeast. In: Cell Biology and Dynamics of Yeast Lipids, ed. Guenther Daum. Research Signpost 37, 161-177.
Iwamoto, M., S. Fairclough, S. Rudge, and J. Engebrecht (2005). The Saccharomyces cerevisiae Sps1p regulates trafficking of enzymes required for spore wall synthesis. Eukaryot. Cell 4,536-44.
Rudge, S., V. Sciorra, M. Iwamoto, C. Zhou, T. Strahl, A. Morris, J. Thorner, and J. Engebrecht (2004). Roles of phosphoinositides and of Spo14p (phospholipase D)-generated phosphatidic acid during yeast sporulation. Mol. Biol. Cell 15, 207-218.
Engebrecht J. (2003). Cell signaling in yeast sporulation. Biochem. Biophys. Res. Commun. 306, 325-328.