David Schlessinger

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David Schlessinger (born September 20, 1936, in Toronto, Canada) is a Canadian-born American biochemist, microbiologist, and geneticist. [1] [2] He is known for his directorship of the development of the map of the X chromosome. [3] [4] [5]

Contents

Biography

His family moved from Toronto to Chicago in 1939. David Schlessinger graduated from Theodore Roosevelt High School in 1953. At the age of 16 he matriculated at the University of Chicago. [1] In 1955 he worked as a paid student-technician in Eugene Goldwasser's laboratory. Schlessinger graduated from the University of Chicago in 1957 with a B.S. in chemistry. At Harvard University he graduated in 1960 with a Ph.D. in biochemistry. [6] According to Schlessinger, his most important achievement "as a graduate student was to develop the first in vitro system that could actually make some little bits of protein" — this system enabled Arthur Kornberg and other researchers to determine the molecular mechanisms of the genetic code. As a graduate student he spent some time at Caltech, where he worked on an experiment that failed. However, at Caltech he did meet a woman who was a plant physiologist and became his wife in 1960. Schlessinger's Ph.D. thesis "Ribosomes from Escheria coli" was supervised by James D. Watson. [1]

As a postdoc, Schlessinger worked at the Pasteur Institute, where he was supervised by Jacques Monod. In August 1962, Schlessinger with his wife and infant daughter, arrived in St. Louis, where he was to spend 35 years as a professor at Washington University in St. Louis. [1] There he was the director of the Human Genome Center from 1987 to 1997. In 1995 he was the president of the American Society for Microbiology (ASM). After his many years in St. Louis as a professor of Molecular Microbiology, Genetics, and Microbiology in Medicine, Schlessinger moved to the National Institute on Aging (NIA) in September 1997. He has done research on microbial genomes, as well as the human genome. At NIA he headed the Laboratory of Genetics from 1997 to 2017. He was instrumental in starting the NIA's SardiNIA Project in 2001 and in retirement continued as an advisor to the project. [3] The purpose of NIA's SardiNIA Project is the identification of "genetic bases for prominent age-associatred changes". [7]

In 1969 he received the Eli Lilly and Company-Elanco Research Award.

Schlessinger and his wife have two daughters and six grandchildren. [1]

Selected publications

Related Research Articles

<span class="mw-page-title-main">Genetic code</span> Rules by which information encoded within genetic material is translated into proteins

The genetic code is the set of rules used by living cells to translate information encoded within genetic material into proteins. Translation is accomplished by the ribosome, which links proteinogenic amino acids in an order specified by messenger RNA (mRNA), using transfer RNA (tRNA) molecules to carry amino acids and to read the mRNA three nucleotides at a time. The genetic code is highly similar among all organisms and can be expressed in a simple table with 64 entries.

<span class="mw-page-title-main">Nucleoid</span> Region within a prokaryotic cell containing genetic material

The nucleoid is an irregularly shaped region within the prokaryotic cell that contains all or most of the genetic material. The chromosome of a typical prokaryote is circular, and its length is very large compared to the cell dimensions, so it needs to be compacted in order to fit. In contrast to the nucleus of a eukaryotic cell, it is not surrounded by a nuclear membrane. Instead, the nucleoid forms by condensation and functional arrangement with the help of chromosomal architectural proteins and RNA molecules as well as DNA supercoiling. The length of a genome widely varies and a cell may contain multiple copies of it.

<span class="mw-page-title-main">Transfer-messenger RNA</span>

Transfer-messenger RNA is a bacterial RNA molecule with dual tRNA-like and messenger RNA-like properties. The tmRNA forms a ribonucleoprotein complex (tmRNP) together with Small Protein B (SmpB), Elongation Factor Tu (EF-Tu), and ribosomal protein S1. In trans-translation, tmRNA and its associated proteins bind to bacterial ribosomes which have stalled in the middle of protein biosynthesis, for example when reaching the end of a messenger RNA which has lost its stop codon. The tmRNA is remarkably versatile: it recycles the stalled ribosome, adds a proteolysis-inducing tag to the unfinished polypeptide, and facilitates the degradation of the aberrant messenger RNA. In the majority of bacteria these functions are carried out by standard one-piece tmRNAs. In other bacterial species, a permuted ssrA gene produces a two-piece tmRNA in which two separate RNA chains are joined by base-pairing.

<span class="mw-page-title-main">Start codon</span> First codon of a messenger RNA translated by a ribosome

The start codon is the first codon of a messenger RNA (mRNA) transcript translated by a ribosome. The start codon always codes for methionine in eukaryotes and archaea and a N-formylmethionine (fMet) in bacteria, mitochondria and plastids.

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<i>trp</i> operon Operon that codes for the components for production of tryptophan

The trp operon is a group of genes that are transcribed together, encoding the enzymes that produce the amino acid tryptophan in bacteria. The trp operon was first characterized in Escherichia coli, and it has since been discovered in many other bacteria. The operon is regulated so that, when tryptophan is present in the environment, the genes for tryptophan synthesis are repressed.

A bacterial initiation factor (IF) is a protein that stabilizes the initiation complex for polypeptide translation.

<span class="mw-page-title-main">5S ribosomal RNA</span> RNA component of the large subunit of the ribosome

The 5S ribosomal RNA is an approximately 120 nucleotide-long ribosomal RNA molecule with a mass of 40 kDa. It is a structural and functional component of the large subunit of the ribosome in all domains of life, with the exception of mitochondrial ribosomes of fungi and animals. The designation 5S refers to the molecule's sedimentation velocity in an ultracentrifuge, which is measured in Svedberg units (S).

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The E-site is the third and final binding site for t-RNA in the ribosome during translation, a part of protein synthesis. The "E" stands for exit, and is accompanied by the P-site which is the second binding site, and the A-site (aminoacyl), which is the first binding site. It is involved in cellular processes.

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References

  1. 1 2 3 4 5 "Schlessinger, David" (PDF). National Human Genome Research Institute (NHGRI, genome.gov). March 2018.
  2. Schlessinger, D. (1996). "Parallel lives: My life in the lab and molecular microbiology". ASM News. 62 (1): 30–32.
  3. 1 2 "David Schlessinger". Principal Investigators, Intramural Research Program, National Institutes of Health. (with sections "Biography" & "Selected Publications")
  4. "Lessons from His First 63 Years in Research: NIA Honors Schlessinger". 13 July 2018.
  5. The NIH Record. U.S. Department of Health and Human Services, National Institutes of Health. 1998.
  6. McGraw-Hill Modern Scientists and Engineers. McGraw-Hill. 1980. p. 79. ISBN   9780070452664.
  7. "The SardiNIA Project". National Institute on Aging (NIA).