Cytochrome c plays an essential role in the energy-yielding electron transfer reactions of mitochondria. Glyceraldehyde 3-P dehydrogenase (GAPDH) is a key glycolytic enzyme important in carbohydrate metabolism and in energy production. This enzyme is especially active in muscle and may be differentially regulated. Our long-term goals are to clone and to determine the DNA sequence of a number of cytochrome c genes and GAPDH genes, as well as their pseudogenes, and to obtain fundamental information on the evolution of genes and pseudogenes. The following organisms, which are representatives of evolutionary periods between major divergence events, will be covered by this and earlier studies: human, monkey, rat, chicken, frog, tuna fish, fruit fly, snail, rice, Arabidopsis, ginkgo and yeast. Two additional goals of this proposal are (a) to study the muscle specific regulation of the GAPDH gene in the fruit fly; and (b) to study the regulation of expressed rat GAPDH pseudogenes that we have discovered. The reasons why we have chosen cytochrome c genes and GAPDH genes for the initial studies are: (a) Over 90 cytochrome c protein sequences and about 10 GAPDH protein sequences are known. (b) Both proteins are relatively highly conserved in both the primary and tertiary structures. (c) Cytochrome c and GAPDH are present in all eucaryotes. For the preceding three reasons, cytochrome c has already served as a useful model for molecular evolutionary analysis. (d) Also, a large number of clones carrying cytochrome c-like or GAPDH-like pseudogene sequences have been isolated in our laboratory. We plan to study more genes and pseudogenes by using a new approach for the identification of a functional gene from among many pseudogenes.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM029179-09
Application #
3276703
Study Section
Genetics Study Section (GEN)
Project Start
1988-04-01
Project End
1991-03-31
Budget Start
1989-04-01
Budget End
1990-03-31
Support Year
9
Fiscal Year
1989
Total Cost
Indirect Cost
Name
Cornell University
Department
Type
Schools of Arts and Sciences
DUNS #
City
Ithaca
State
NY
Country
United States
Zip Code
14850
Wang, Y; Zhang, W; Cao, J et al. (1992) Characterization of cis-acting elements regulating transcription from the promoter of a constitutively active rice actin gene. Mol Cell Biol 12:3399-406
Zhang, W; McElroy, D; Wu, R (1991) Analysis of rice Act1 5' region activity in transgenic rice plants. Plant Cell 3:1155-65
McElroy, D; Blowers, A D; Jenes, B et al. (1991) Construction of expression vectors based on the rice actin 1 (Act1) 5' region for use in monocot transformation. Mol Gen Genet 231:150-60
Reece, K S; McElroy, D; Wu, R (1990) Genomic nucleotide sequence of four rice (Oryza sativa) actin genes. Plant Mol Biol 14:621-4
McElroy, D; Rothenberg, M; Reece, K S et al. (1990) Characterization of the rice (Oryza sativa) actin gene family. Plant Mol Biol 15:257-68
McElroy, D; Rothenberg, M; Wu, R (1990) Structural characterization of a rice actin gene. Plant Mol Biol 14:163-71
McElroy, D; Zhang, W; Cao, J et al. (1990) Isolation of an efficient actin promoter for use in rice transformation. Plant Cell 2:163-71
Xie, Y; Wu, R (1990) Molecular analysis of an alcohol dehydrogenase-encoding genomic clone (adh2) from rice. Gene 87:185-91
Xie, Y; Wu, R (1989) Rice alcohol dehydrogenase genes: anaerobic induction, organ specific expression and characterization of cDNA clones. Plant Mol Biol 13:53-68
Moon, E; Kao, T H; Wu, R (1988) Rice mitochondrial genome contains a rearranged chloroplast gene cluster. Mol Gen Genet 213:247-53

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