Please use this identifier to cite or link to this item: https://hdl.handle.net/20.500.12104/43480
Title: Isoform-specific regulation of a steroid hormone nuclear receptor by an E3 ubiquitin ligase in Drosophila melanogaster
Author: Leal, C.A.
Belmont, J.W.
Nachtman, R.
Cantu, J.M.
Medina, C.
Issue Date: 1994
Abstract: Five polymorphic index markers were analyzed by polymerase chain reaction (PCR) to ascertain the parental origin of the extra X chromosomes in seven polysomic cases (one 49,XXXXX, three 49,XXXXY, two 48,XXXY, and one 48, XXYY). All four X chromosomes in 49, X polysomies were maternal in origin and the extra X chromosomes in 48 X polysomies were paternal. In each case the multiple X chromosomes were contributed by a single parent. Taken together with previously reported cases, these data support a single mechanism of sequential nondisjunction during either maternal or paternal gametogenesis as the cause of higher order sex chromosome polysomy. " 1994 Springer-Verlag.",,,,,,"10.1007/BF00201605",,,"http://hdl.handle.net/20.500.12104/43480","http://www.scopus.com/inward/record.url?eid=2-s2.0-0027994243&partnerID=40&md5=5fdd3a6dfe7ea53e46f9ffebd47caf02",,,,,,"4",,"Human Genetics",,"423
426",,"94",,"Scopus",,,,,,,,,,,,"Parental origin of the extra chromosomes in polysomy X",,"Article" "44189","123456789/35008",,"Gradilla, A.-C., Instituto Cajal, Consejo Superior de Investigaciones Científicas, Madrid 28002, Spain, Universidad de Guadalajara, Jalisco 44600, Mexico; Mansilla, A., Instituto Cajal, Consejo Superior de Investigaciones Científicas, Madrid 28002, Spain; Ferr s, A., Instituto Cajal, Consejo Superior de Investigaciones Científicas, Madrid 28002, Spain",,"Gradilla, A.-C.
Mansilla, A.
Ferrus, A.",,"2011",,"The steroid hormone 20-hydroxyecdysone (20E) regulates gene transcription through the heterodimeric nuclear receptor composed of ecdysone receptor (EcR) and Ultraspiracle (USP). The EcR gene encodes three protein isoforms-A, B1, and B2-with variant N-terminal domains that mediate tissue and developmental stage-specific responses to 20E. Ariadne-1a is a conserved member of the RING finger family of ubiquitin ligases first identified in Drosophila melanogaster. Loss-of-function mutations at key cysteines in either of the two RING finger motifs, as well as general overexpression of this enzyme, cause lethality in pupae, which suggests a requirement in metamorphosis. Here, we show that Ariadne-1a binds specifically the isoform A of EcR and ubiquitylates it. Coimmunoprecipitation experiments indicate that the full sequence of EcRA is required for this binding. Protein levels of EcRA and USP change in opposite directions when those of ARI-1a are genetically altered. This is an isoform-specific, E3-dependent regulatory mechanism for a steroid nuclear receptor. Further, qRT-PCR experiments show that the ARI-1a levels lead to the transcriptional regulation of Eip78C, Eip74EF, Eip75B, and Br-C, as well as that of EcR and usp genes. Thus, the activity of this enzyme results in the regulation of dimerizing receptors at the protein and gene transcription levels. This fine-tuned orchestration by a conserved ubiquitin ligase is required during insect metamorphosis and, likely, in other steroid hormone-controlled processes across species. " 2011 by the Genetics Society of America.
URI: http://hdl.handle.net/20.500.12104/42410
http://www.scopus.com/inward/record.url?eid=2-s2.0-81255176718&partnerID=40&md5=6b7362db60ec5ab6d8347e6f387cbb83
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