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Chromosome localizations of genes for five cAMP-specific phosphodiesterases in man and mouse
Authors:Athena Milatovich  Graeme Bolger  Tamar Michaeli  Uta Francke
Institution:(1) Department of Genetics, Stanford University Medical Center, 94305 Stanford, California;(2) Pediatrics, Stanford University Medical Center, 94305 Stanford, California;(3) Howard Hughes Medical Institute, Stanford University Medical Center, 94305 Stanford, California;(4) Cold Spring Harbor Laboratory, Cold Spring Harbor, 11724 New York;(5) Present address: Division of Genetics, Cincinnati Children's Hospital, 45229 Cincinnati, Ohio;(6) Present address: Hematology-Oncology Division, School of Medicine, University of Utah, 84132 Salt Lake City, Utah;(7) Present address: Department of Developmental Biology and Cancer, Albert Einstein College of Medicine, 10461 Bronx, New York
Abstract:Cyclic nucleotides are important second messengers that mediate a number of cellular responses to external signals. Cyclic nucleotide phosphodiesterases play a role in signal transduction by regulating the cellular concentrations of these messengers. Here, we have applied Southern analyses of somatic cell hybrid lines and of recombinant inbred (RI) mouse strains as well as fluorescence chromosomal in situ hybridization (FISH) to chromosomally localize five cAMP-specific nucleotide phosphodiesterase genes in human and mouse. GenesDPDE1, DPDE2, DPDE3, andDPDE4 that share sequence homology with theDrosophila dunce gene were assigned to human chromosomes 19 (DPDE1 andDPDE2), 5q12 (DPDE3), and 1p31 (DPDE4) and to mouse chromosomes 8, 9, 13, and 4, respectively. The high-affinity cAMP-specific phosphodiesterase gene (HCP1) was mapped to human chromosome 8q13-q22. Since these genes are potential candidates for involvement in psychiatric or behavioral disorders, knowledge of their chromosomal localizations will facilitate the discovery of their association with disease genes as they are being mapped by linkage studies.
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