Cloning, Characterization, and Functional Study of Laminin a Chain in Hydra
Date of Graduation
Summer 1998
Degree
Master of Science in Biology
Department
Biology
Committee Chair
Xiaoming Zhang
Abstract
Hydra vulgaris, a fresh water cnidarian, was used in this study of extracellular matrix (ECM) molecular functions at the genetic level. To clone ECM genes, screening of a hydra cDNA library was accomplished by using a laminin A chain sequence obtained from polymerase chain reaction as a probe. A clone, 1am A1, was sequenced and characterized in this project. In situ hybridization studies indicated that the laminin A chain messenger RNA is located in the endoderm. A high level of expression is observed at the base of the tentacles, which indicates that the ECM molecule, laminin, may participate in the patterning process of hydra tentacles, cell migration, and cell differentiation processes of nematocytes. Decapitation and regeneration studies indicated that the range of expression of laminin A chain along the tentacles varies at different regeneration stages, from the entire length of tentacles at early stages to the base of tentacles when they reach the mature stage. The expression pattern change suggests control factors related to the maintenance of the tentacle branching mechanism or to the cell differentiation and cell migration processes.
Subject Categories
Biology
Copyright
© Brooke D Bigler
Recommended Citation
Bigler, Brooke D., "Cloning, Characterization, and Functional Study of Laminin a Chain in Hydra" (1998). MSU Graduate Theses/Dissertations. 216.
https://bearworks.missouristate.edu/theses/216
Dissertation/Thesis