Bypass navigation and tool bar
NIDDK logo
navigation bar Home Welcome Health Information Research Funding Opportunities (Extramural) Clinical Trials You are here: NIDDK Laboratories (Intramural) Reports, Testimony & Plans
National Institutes of Health
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Site Map FAQs Contact NIDDK
NIDDK Home  : NIDDK Laboratories : Faculty : Herbert Tabor, M.D.

Herbert Tabor, M.D.

Pharmacology Section, Chief
Laboratory of Biochemistry and Genetics
NIDDK, National Institutes of Health
Building 8, Room 223
Bethesda, MD 20892-0830
Tel:301-496-2562
Email:  tabor@helix.nih.gov
B.A., Harvard University, 1948
M.D., Harvard University, 1948

Research Statement

The polyamines, putrescine, spermidine, and spermine, are major polybasic compounds in all living cells. These amines have been shown to be important for many systems related to growth and differentiation. We have been interested in how these polyamines are synthesized, how their biosynthesis and degradation are regulated, their physiologic functions, and how they act in vivo. For this purpose we have constructed null mutants in each of the biosynthetic steps in both Escherichia coli and in Saccharomyces cerevisiae. These mutants are unable to make these amines, and hence they are very useful tools to study the physiological effects due to their deprivation. Our present studies are directed at extending our studies on the biochemistry, regulation, and genetics of these amines and of the biosynthetic enzymes in S. cerevisiae. Our older work plus our current work has demonstrated that the polyamines are required for growth of the organisms, for sporulation, for maintenance of the killer dsRNA virus, for protection against oxidative damage, for protection against elevated temperatures, for fidelity of protein biosynthesis, and for the maintenance of mitochondria. Clones have been constructed that overproduce the various enzymes, and the sequence and structural characteristics of these enzymes have been studied. We have concentrated particularly on the structure and regulation of ornithine decarboxylase, spermidine synthase, spermine synthase, and S-adenosylmethionine decarboxylase.

Back to Top

Publications

1. Hamasaki-Katagiri N Katagiri Y Tabor CW Tabor H  Spermine is not essential for growth of Saccharomyces cerevisiae: identification of the SPE4 gene (spermine synthase) and characterization of a spe4 deletion mutant.  Gene (210): 195-201, 1998. [Full Text/Abstract]

2. Balasundaram D Dinman JD Wickner RB Tabor CW Tabor H  Spermidine deficiency increases +1 ribosomal frameshifting efficiency and inhibits Ty1 retrotransposition in Saccharomyces cerevisiae.  Proc Natl Acad Sci U S A (91): 172-6, 1994. [Full Text/Abstract]

3. Xie QW Tabor CW Tabor H  Deletion mutations in the speED operon: spermidine is not essential for the growth of Escherichia coli.  Gene (126): 115-7, 1993. [Full Text/Abstract]

4. Xie QW Tabor CW Tabor H  Ornithine decarboxylase in Saccharomyces cerevisiae: chromosomal assignment and genetic mapping of the SPE1 gene.  Yeast (6): 455-60, 1990. [Full Text/Abstract]

5. Tabor CW Tabor H  The speEspeD operon of Escherichia coli. Formation and processing of a proenzyme form of S-adenosylmethionine decarboxylase.  J Biol Chem (262): 16037-40, 1987. [Full Text/Abstract]


Back to Top


Director: Dr. Allen Spiegel || Contact NIDDK
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) is part of the National Institutes of Health, Bethesda, MD, USA. General inquiries may be addressed to Office of Communications and Public Liaison, NIDDK, NIH, Building 31, room 9A04 Center Drive, MSC 2560, Bethesda, MD 20892-2560, USA. || Privacy || Disclaimer || Copyright || Credits || Accessibility

U. S. National Institutes of Health U.S. Department of Health & Human Services FirstGov