This project has two closely related aims (1) to seek a better understanding of the evolutionary relationship of the primates through analysis of the structure and expression of the globin genes during embryonic and fetal development; and (2) to follow clues about the controlling gene elements that determine when genes are turned on and off during gestation by observing differences in the timing of gene expression in these closely related animals. The research focuses on the globin genes, since they undergo a well-characterized sequence of switches during gestation in humans, and the control (reversal) of these switches may have significant medical benefits in hematological diseases such as sickle cell anemias and thalassemia. Expression profiles in the two branches of simian primates, catarrhines (Old World Monkeys, hominoids) and platyrrhines (New World Monkeys), suggests that more than one step was involved in the evolutionary transition. We are (1) localizing fe tal-speci fic sequences within the human ( gene; (2) using the strategy called differential phylogenetic footprinting to identify specific base changes that may be responsible for the three different patterns of ( expression seen in nonanthropoid primates; and (3) documenting the in vivo expression patterns of ( genes in extant platyrrhine and catarrhine primates. This work has important implications for clarifying the mechanisms that control new patterns of gene expression as well as for the understanding of factors that regulate hemoglobin switching. Using samples from the University of Washington Primate Center, we have found that globin gene expression is very similar in M. nemestrina and in humans (1) the expression is fetal; (2) (1 is expressed to a much higher level than (2; and (3) the intergenic distance is 11 kb. FUNDING NIH grants HL33940 and RR00166 and NSF grant INT-9602913. Goodman, M., Porter, C.A., Czelusniak, J., Page, S.L., Schneider, H., Shoshani, J., Gunnell, G., and Groves, C.P. Toward a phylogenetic classification of primates based on DNA evidence complemented by fossil evidence. Mol. Phylogenet. & Evol. 9:585-598, 1998. Goodman, M. The Genomic Record of Humankind's Evolutionary Roots. Am. J. Hum. Genetics 64:31-39, 1999.

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
Primate Research Center Grants (P51)
Project #
3P51RR000166-38S1
Application #
6219726
Study Section
Project Start
1999-05-01
Project End
2000-04-30
Budget Start
1998-10-01
Budget End
1999-09-30
Support Year
38
Fiscal Year
1999
Total Cost
Indirect Cost
Name
University of Washington
Department
Type
DUNS #
135646524
City
Seattle
State
WA
Country
United States
Zip Code
98195
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Raghanti, Mary Ann; Edler, Melissa K; Stephenson, Alexa R et al. (2018) A neurochemical hypothesis for the origin of hominids. Proc Natl Acad Sci U S A 115:E1108-E1116
Wool, Lauren E; Crook, Joanna D; Troy, John B et al. (2018) Nonselective Wiring Accounts for Red-Green Opponency in Midget Ganglion Cells of the Primate Retina. J Neurosci 38:1520-1540
Hasegawa, Yu; Curtis, Britni; Yutuc, Vernon et al. (2018) Microbial structure and function in infant and juvenile rhesus macaques are primarily affected by age, not vaccination status. Sci Rep 8:15867
Oleskiw, Timothy D; Nowack, Amy; Pasupathy, Anitha (2018) Joint coding of shape and blur in area V4. Nat Commun 9:466
Eberle, R; Jones-Engel, L (2017) Understanding Primate Herpesviruses. J Emerg Dis Virol 3:
McAdams, Ryan M; McPherson, Ronald J; Kapur, Raj P et al. (2017) Focal Brain Injury Associated with a Model of Severe Hypoxic-Ischemic Encephalopathy in Nonhuman Primates. Dev Neurosci 39:107-123

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