Roger M. Wartell | |
---|---|
Born | New York, New York |
Nationality | American |
Alma mater | Stevens Institute of Technology University of Rochester |
Known for | Development of TGGE |
Scientific career | |
Fields | RNA Based Regulation of Gene Expression |
Institutions | Georgia Tech |
Doctoral advisor | Elliott Waters Montroll |
Roger Martin Wartell is the former chair of the school of biology, part of the College of Sciences at the Georgia Institute of Technology.
Roger Wartell was born in New York, New York. He received his B.S. degree in physics from Stevens Institute of Technology in 1966. In 1971 he received his Ph.D. in physics from the University of Rochester, where he worked in the group of Elliott Waters Montroll on the DNA helix-coil transition. From 1971 to 1973 he was a NIH postdoctoral fellow in the laboratory of Robert Wells at the University of Wisconsin-Madison. He was a visiting professor at the University of Wisconsin-Madison in 1978–1979, and visiting scholar at National Institutes of Health-Bethesda from 1987 to 1988. [1]
Wartell joined the faculty at Georgia Tech in 1974, and received a NIH Career Development Award in 1979. He served as associate chair of the Georgia Institute of Technology School of Physics from 1987 to 1988. With a 1/3 joint appointment in biology, he was appointed acting chair of the Georgia Tech School of Biology in 1990. Under his tenure as chair (1990–2004), the undergraduate curriculum was revised to provide students with three areas of emphasis: environmental biology, microbiology, and molecular biology and faculty size increased from 12 to 26. The areas reflected the research and educational interests of the faculty.
He is a member of the NASA Astrobiology Institute at Georgia Tech. His research is focused on protein-RNA interactions in gene regulation, ribosomal evolution, and ribozyme reactions in ice.
A base pair (bp) is a fundamental unit of double-stranded nucleic acids consisting of two nucleobases bound to each other by hydrogen bonds. They form the building blocks of the DNA double helix and contribute to the folded structure of both DNA and RNA. Dictated by specific hydrogen bonding patterns, "Watson–Crick" base pairs allow the DNA helix to maintain a regular helical structure that is subtly dependent on its nucleotide sequence. The complementary nature of this based-paired structure provides a redundant copy of the genetic information encoded within each strand of DNA. The regular structure and data redundancy provided by the DNA double helix make DNA well suited to the storage of genetic information, while base-pairing between DNA and incoming nucleotides provides the mechanism through which DNA polymerase replicates DNA and RNA polymerase transcribes DNA into RNA. Many DNA-binding proteins can recognize specific base-pairing patterns that identify particular regulatory regions of genes.
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