ANALYSIS OF THE WORM LAMININ beta GENE. Gautam Kao1, Edward Hedgecock2, and Bill Wadsworth1. 1Dept. of Pathology, Robert Wood Johnson Medical School, Piscataway, NJ 08854. 2Dept. of Biology, Johns Hopkins University, Baltimore, MD 212 18. The basement membrane is a sheath of extracellular material that provides a connection between cells and the external environment. The heterotrimeric glycoprotein, laminin forms part of the scaffold structure of the basement membrane and interacts with cells via receptors such as integrins. The analysis of the function of laminin will provide some insights into the crucial roles the extracellular matrix has in controlling neuronal pathfinding, organogenesis, muscle positioning, tissue separation and the distribution of developmental signals. The three subunits of laminin: alpha, beta, gamma (previously known as A, B 1 and B2 respectively) have been cloned from a number of organisms. There is a high degree of sequence conservation for each subunit across the phylogenetic spectrum. The beta subunit consists of two globular domains ( the N-terminal domain VI and domain IV) two stretches of EGF like repeats (domain III and domain IV) and two a- helical regions (domains II and I) We have previously described the isolation of a DNA fragment that shows homology with the domain VI region of vertebrate and insect laminin beta genes. This DNA was physically mapped to cosmid C24D10 on chromosome IV near
dpy-13 (1). A homozygous viable mutation in the gene lam-l (
rh219) was isolated in a screen for new mutants linked to
dpy-13.
rh219 mutants share phenotypic characteristics with mutants of epi-l the laminin a chain gene (2). Furthermore, genetic interactions have been observed between epi-l and lam-l mutants.
rh219 is a reduction-of-function mutation since
rh219/Df animals die as larvae. These molecular and genetic obsenrations suggest that there is a laminin alpha chain gene on C24D10 and that it corresponds to lam-l . We tested the ability C24D10 to rescue
rh219 defects by crossing a cosmid bearing array into mutant animals. Array containing
rh219 animals are fully rescued for egg laying ability and locomotion. Sequencing of the domain VI region of the gene shows greater than 50% sequence identity with the fruifly and mouse genes. This sequence includes a well conserved transition from domain VI to domain V. In order to better understand the phenotypic consequences of the
rh219 mutation, we are examining the mutant by electron microscopy. Preliminary results revealed the presence of several defects that are reminiscent of the phenotype of epi- l mutants and are consistent with the notion that the basement membrane is defective. These defects include the following: a) Whorls of matrix material are seen delaminated from the basement membrane. b) Muscle cells are seen in abnormal positions. c) The excretory canals are abnormal, either having a completely collapsed lumen, or failing to grow out properly. d) There appears to be abnormally high levels of yolk in the intestine perhaps as a result of decreased transport of yolk to the gonad. e) The sheath cells are abnormal in structure. In addition the proximal region of the gonad that normally contains meiotic germ cells, instead contains immature mitotic cells. Thanks to David Hall for his help in interpreting the EM pictures. (1). L. Gong, W. Wadsworth, and E. Hedgecock (1991). 8th International C. elegans. Meeting,pg 116. (2). K. Joh, and E. Hedgecock (1993). 9th International C. elegans. Meeting, pg 222