This application is for partial support of the research in four laboratories in the M.I.T. Cancer Center. The central focus of all the projects is to apply the methods of cell and molecular biology to questions concerning the structure, function, subcellular localization and interactions of proteins important for the behavior of normal and malignant cells. 1. The expression and function of different alternatively spliced forms of fibronectin and of fibronectin receptors will be investigated. The control of the splicing process and the functions of variable segments of fibronectin and of the different subunits of the receptors will be analyzed. 2. Structure-function relationships of NaKATPase subunits and isoforms will be studied. The nature of ouabain resistance will be investigated using gene transfer techniques, site-specific mutagenesis and mutant selection. 3. Functions involved in the intracellular processing of glycoproteins will be analyzed, specifically functions of the endoplasmic reticulum and Golgi apparatus and targeting elements in the glycoproteins will be studied. The effects of various manipulations on glycoprotein processing will be investigated. 4. The structure, variation and functions of chartins, a class of microtubule associated proteins will be investigated. cDNAs for these proteins will be cloned and used to study the properties of this protein family. The basis for the assembly of ordered microtubule arrays will be analyzed in the marginal band of erythrocytes. In these studies, specific probes; recombinant DNA; antibodies; synthetic peptides; etc. will be employed as will be the methods of genetic engineering.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Program Projects (P01)
Project #
5P01CA026712-11
Application #
3093145
Study Section
Special Emphasis Panel (SRC (X1))
Project Start
1979-12-01
Project End
1990-12-31
Budget Start
1989-12-01
Budget End
1990-12-31
Support Year
11
Fiscal Year
1990
Total Cost
Indirect Cost
Name
Massachusetts Institute of Technology
Department
Type
Organized Research Units
DUNS #
City
Cambridge
State
MA
Country
United States
Zip Code
02139
Jackson, B J; Kukuruzinska, M A; Robbins, P (1993) Biosynthesis of asparagine-linked oligosaccharides in Saccharomyces cerevisiae: the alg2 mutation. Glycobiology 3:357-64
Moremen, K W; Robbins, P W (1991) Isolation, characterization, and expression of cDNAs encoding murine alpha-mannosidase II, a Golgi enzyme that controls conversion of high mannose to complex N-glycans. J Cell Biol 115:1521-34
Moremen, K W; Touster, O; Robbins, P W (1991) Novel purification of the catalytic domain of Golgi alpha-mannosidase II. Characterization and comparison with the intact enzyme. J Biol Chem 266:16876-85
Orlean, P; Kuranda, M J; Albright, C F (1991) Analysis of glycoproteins from Saccharomyces cerevisiae. Methods Enzymol 194:682-97
Guan, J L; Trevithick, J E; Hynes, R O (1991) Fibronectin/integrin interaction induces tyrosine phosphorylation of a 120-kDa protein. Cell Regul 2:951-64
Guan, J L; Hynes, R O (1990) Lymphoid cells recognize an alternatively spliced segment of fibronectin via the integrin receptor alpha 4 beta 1. Cell 60:53-61
Fukuda, M N; Masri, K A; Dell, A et al. (1990) Incomplete synthesis of N-glycans in congenital dyserythropoietic anemia type II caused by a defect in the gene encoding alpha-mannosidase II. Proc Natl Acad Sci U S A 87:7443-7
Norton, P A; Hynes, R O (1990) In vitro splicing of fibronectin pre-mRNAs. Nucleic Acids Res 18:4089-97
Bischoff, J; Moremen, K; Lodish, H F (1990) Isolation, characterization, and expression of cDNA encoding a rat liver endoplasmic reticulum alpha-mannosidase. J Biol Chem 265:17110-7
Guan, J L; Trevithick, J E; Hynes, R O (1990) Retroviral expression of alternatively spliced forms of rat fibronectin. J Cell Biol 110:833-47

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