The Q cell migrations in C elegans provide a wonderful opportunity to investigate fundamental aspects of cell patterning and positioning. The QL and QR neuroblasts are bilateral homologs that migrate in opposite directions. QR and its descendants migrate anteriorly, whereas QL and its descendants migrate posteriorly. During its migration, QL switches on the Hox gene mab-5, which, in turn, causes QL's descendants to migrate posteriorly instead of anteriorly. Ultimately, each Q-cell descendant migrates to a unique anteroposterior (A/P) position that does not correspond to any obvious landmarks. Thus, by studying Q cell migration, we can ask how left-right asymmetry is generated, how Hox gene regulation and function are integrated into a biological process, how guidance information can direct these complex migrations, and how guidance cues polarize the cytoskeleton and control cell movement. During this past funding period, we have found that these migrations are regulated by many interesting signaling proteins, both novel and conserved. These include Wnt pathway members, a netrin receptor, novel transmembrane proteins required for cell positioning and for left-right asymmetry, and a Rho family member, exchange factor, and integrin receptors required for migration itself. Many of the conserved signaling molecules behave in unexpected ways, making them especially interesting to investigate. During this funding period, we will identify missing components of this system by exploiting a rapid new screening procedure. In addition, by manipulating expression of genes we have characterized, we will ask how Q migration is regulated. For example, we will ask whether particular proteins specify left-right asymmetry, and whether extracellular guidance cues have permissive or instructive roles. In addition, we will investigate the functions of proteins that appear to polarize and move the Q cells by using GFP fusions to visualize intracellular events. Together these studies should help to define the molecular mechanisms that regulate and execute these migrations.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
2R01GM037053-13
Application #
2695949
Study Section
Genetics Study Section (GEN)
Project Start
1986-09-01
Project End
2002-08-31
Budget Start
1998-09-01
Budget End
1999-08-31
Support Year
13
Fiscal Year
1998
Total Cost
Indirect Cost
Name
University of California San Francisco
Department
Biochemistry
Type
Schools of Medicine
DUNS #
073133571
City
San Francisco
State
CA
Country
United States
Zip Code
94143
Yang, Lucie; Sym, Mary; Kenyon, Cynthia (2005) The roles of two C. elegans HOX co-factor orthologs in cell migration and vulva development. Development 132:1413-28
Ch'ng, QueeLim; Williams, Lisa; Lie, Yung S et al. (2003) Identification of genes that regulate a left-right asymmetric neuronal migration in Caenorhabditis elegans. Genetics 164:1355-67
Alper, Scott; Kenyon, Cynthia (2002) The zinc finger protein REF-2 functions with the Hox genes to inhibit cell fusion in the ventral epidermis of C. elegans. Development 129:3335-48
Alper, S; Kenyon, C (2001) REF-1, a protein with two bHLH domains, alters the pattern of cell fusion in C. elegans by regulating Hox protein activity. Development 128:1793-804
Whangbo, J; Harris, J; Kenyon, C (2000) Multiple levels of regulation specify the polarity of an asymmetric cell division in C. elegans. Development 127:4587-98
Whangbo, J; Kenyon, C (1999) A Wnt signaling system that specifies two patterns of cell migration in C. elegans. Mol Cell 4:851-8
Ch'ng, Q; Kenyon, C (1999) egl-27 generates anteroposterior patterns of cell fusion in C. elegans by regulating Hox gene expression and Hox protein function. Development 126:3303-12
Hunter, C P; Harris, J M; Maloof, J N et al. (1999) Hox gene expression in a single Caenorhabditis elegans cell is regulated by a caudal homolog and intercellular signals that inhibit wnt signaling. Development 126:805-14
Maloof, J N; Whangbo, J; Harris, J M et al. (1999) A Wnt signaling pathway controls hox gene expression and neuroblast migration in C. elegans. Development 126:37-49
Herman, M A; Ch'ng, Q; Hettenbach, S M et al. (1999) EGL-27 is similar to a metastasis-associated factor and controls cell polarity and cell migration in C. elegans. Development 126:1055-64

Showing the most recent 10 out of 19 publications