The long-term goal is to be able to use the sequence of a DNA or RNA to predict its three dimensional structure in its natural cellular or extracellular environment. As structure implies function, one can then understand and learn to control its biological function. The synthesis of every protein is specified by a messenger RNA. The messenger RNA is produced by processing a primary transcript transcribed from DNA. The specific folded conformations of these nucleic acids are essential for their correct function. Replication of RNA viruses and DNA viruses requires synthesis of RNA molecules. Thus, knowledge of the sequence and folding of a pathogenic viral RNA can reveal methods for preventing viral replication, and curing or preventing the viral disease. Genetic diseases and autosomal genetic diseases, such as cancer, are caused by a change in sequence of DNA. It is vital to understand how the changes in sequence can occur, and what the effects of these changes are on the replication and transcription of the DNA, and on the processing and translation of the RNA. The relation between nucleic acid sequence and conformation, and its role in protein sequence is central to many problems of human health. Oligonucleotides will be synthesized that can form important structural motifs present in RNA and DNA. Their sequences and their environments will be varied to determine what structures do form and what conditions are required for their formation. Reactivity of the oligonucleotides to enzymes and to chemical reagents will reveal double strand and single strand regions. Spectroscopic measurements, conformations. Thermodynamic parameters which characterize the stabilities of the different motifs will exchange between different conformations will be determined by NMR, or by temperature-jump methods. The structural elements to be studied in RNA include pseudoknots, hairpin loops, base-base mismatches, internal loops, bulges, and left-handed Z-RNA. In DNA the motifs include base-base mismatches, telomeric sequences, and two-, three- and four-stranded complexes involving guanine base pairs.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Method to Extend Research in Time (MERIT) Award (R37)
Project #
5R37GM010840-40
Application #
2608699
Study Section
Special Emphasis Panel (NSS)
Project Start
1976-12-01
Project End
1999-11-30
Budget Start
1997-12-01
Budget End
1998-11-30
Support Year
40
Fiscal Year
1998
Total Cost
Indirect Cost
Name
University of California Berkeley
Department
Chemistry
Type
Schools of Arts and Sciences
DUNS #
094878337
City
Berkeley
State
CA
Country
United States
Zip Code
94704
Yan, Shannon; Wen, Jin-Der; Bustamante, Carlos et al. (2015) Ribosome excursions during mRNA translocation mediate broad branching of frameshift pathways. Cell 160:870-881
Goldman, Daniel H; Kaiser, Christian M; Milin, Anthony et al. (2015) Ribosome. Mechanical force releases nascent chain-mediated ribosome arrest in vitro and in vivo. Science 348:457-60
Tinoco Jr, Ignacio (2015) The ethical scientist: An old-fashioned view. Biopolymers 103:424-31
Tinoco Jr, Ignacio (2014) Fun and games in Berkeley: the early years (1956-2013). Annu Rev Biophys 43:1-17
Kaiser, Christian M; Tinoco Jr, Ignacio (2014) Probing the mechanisms of translation with force. Chem Rev 114:3266-80
Kim, Hee-Kyung; Liu, Fei; Fei, Jingyi et al. (2014) A frameshifting stimulatory stem loop destabilizes the hybrid state and impedes ribosomal translocation. Proc Natl Acad Sci U S A 111:5538-43
Liu, Tingting; Kaplan, Ariel; Alexander, Lisa et al. (2014) Direct measurement of the mechanical work during translocation by the ribosome. Elife 3:e03406
Tinoco, Ignacio; Chen, Gang; Qu, Xiaohui (2010) RNA reactions one molecule at a time. Cold Spring Harb Perspect Biol 2:a003624
Chen, Gang; Chang, Kung-Yao; Chou, Ming-Yuan et al. (2009) Triplex structures in an RNA pseudoknot enhance mechanical stability and increase efficiency of -1 ribosomal frameshifting. Proc Natl Acad Sci U S A 106:12706-11
Tinoco Jr, Ignacio; Wen, Jin-Der (2009) Simulation and analysis of single-ribosome translation. Phys Biol 6:025006

Showing the most recent 10 out of 67 publications