TY - JOUR
T1 - Unusual topography of bovine rhodopsin promoter-IacZ fusion gene expression in transgenic mouse retinas
AU - Zack, Donald J.
AU - Bennett, Jean
AU - Wang, Yanshu
AU - Davenport, Carol
AU - Klaunberg, Brenda
AU - Gearhart, John
AU - Nathans, Jeremy
N1 - Funding Information:
We wish to thank Drs. Paul Hargrave and Jacques Peschon for their kind gifts of monoclonal antibody B6-30and plasmid placF, respectively; Drs. Mary Blue, Mary-Lou Oster-Granite, Mark Mol-iver, and Mary Ann Wilson for generously sharing their neuroanatomical expertise; Dr. Clark Riley and Ms. Anatoli Collector for the timely synthesis of DNA oligomers; Mr. Frederick Dubs for his photographic expertise; Mr. Lester Dyer for his graphic arts expertise; and Ms. Terri Chase for help in the preparation of this manuscript. This work was supported by a Physician Scientist Award (EY00297) from the National Eye Institute (D. J. Z.) and by funds from the Howard Hughes Medical Institute (J. N.).
PY - 1991/2
Y1 - 1991/2
N2 - To define the cis-acting DNA elements required for rhodopsin expression, we generated lines of transgenic mice carrying sequences upstream of the bovine rhodopsin gene fused to the E. coli β-galactosidase gene (IacZ). Upstream sequences extending from -2174 to +70 bp, from -734 to +70 bp, and from -222 to +70 by direct photoreceptor-specific expression. All three -2174 lines demonstrate a superior-temporal to inferior-nasal gradient of expression across the retina, whereas lines carrying the shorter constructs demonstrate either spatially continuous expression across the retina, discrete clusters of expression, or both. As a complementary approach to defining regulatory elements, we compared DNA sequences 5′ of the murine, bovine, and human rhodopsin genes. Significant homology between all three species was found just upstream of the transcription start site and at approximately 1.5 kb upstream.
AB - To define the cis-acting DNA elements required for rhodopsin expression, we generated lines of transgenic mice carrying sequences upstream of the bovine rhodopsin gene fused to the E. coli β-galactosidase gene (IacZ). Upstream sequences extending from -2174 to +70 bp, from -734 to +70 bp, and from -222 to +70 by direct photoreceptor-specific expression. All three -2174 lines demonstrate a superior-temporal to inferior-nasal gradient of expression across the retina, whereas lines carrying the shorter constructs demonstrate either spatially continuous expression across the retina, discrete clusters of expression, or both. As a complementary approach to defining regulatory elements, we compared DNA sequences 5′ of the murine, bovine, and human rhodopsin genes. Significant homology between all three species was found just upstream of the transcription start site and at approximately 1.5 kb upstream.
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U2 - 10.1016/0896-6273(91)90355-4
DO - 10.1016/0896-6273(91)90355-4
M3 - Article
C2 - 1899580
AN - SCOPUS:0026090702
SN - 0896-6273
VL - 6
SP - 187
EP - 199
JO - Neuron
JF - Neuron
IS - 2
ER -