A novel growth hormone receptor subtype in black seabream: cDNA cloning, regulation of gene expression and its disruption by environmental estrogens.

In the tissue distribution study, the expression of GHR2 is significantly higher than GHR1 in many tissues of the seabream including the gonad, kidney, muscle, pituitary and spleen. In vivo hormone treatment data indicated that cortisol and testosterone have differential expression regulation betwee...

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Bibliographic Details
Other Authors: Jaio, Baowei.
Format: Others
Language:English
Chinese
Published: 2006
Subjects:
Online Access:http://library.cuhk.edu.hk/record=b6074207
http://repository.lib.cuhk.edu.hk/en/item/cuhk-343836
id ndltd-cuhk.edu.hk-oai-cuhk-dr-cuhk_343836
record_format oai_dc
collection NDLTD
language English
Chinese
format Others
sources NDLTD
topic Cloning
Estrogen
Genetic regulation
Somatotropin--Receptors
Sparidae
spellingShingle Cloning
Estrogen
Genetic regulation
Somatotropin--Receptors
Sparidae
A novel growth hormone receptor subtype in black seabream: cDNA cloning, regulation of gene expression and its disruption by environmental estrogens.
description In the tissue distribution study, the expression of GHR2 is significantly higher than GHR1 in many tissues of the seabream including the gonad, kidney, muscle, pituitary and spleen. In vivo hormone treatment data indicated that cortisol and testosterone have differential expression regulation between GHR1 and GHR2. On the other hand, hepatic expression of both GHR1 and GHR2 in seabream was decreased by estradiol treatment. In primary cultures of seabream hepatocytes, the expression patterns after treatment by the various concentrations of hormones were consistent with the in vivo results. === To study the actions of environmental estrogens on the somatotropic axis, a transgenic yeast system was developed for estrogenicity screening. The fish estrogen receptor (gfER) and a reporter vector containing the estrogen responsive element (ERE) were expressed in yeast cells as a means to identify potential estrogens. Using this system, more than fifty chemicals including pesticides, herbicides, industrial chemicals and phytoestrogens were screened. Ten compounds including dibutyl phthalate (DBP) and bisphenol A (BPA) were demonstrated to exhibit estrogenic activities. And a compound (malachite green, MG) with novel anti-estrogenenic activities was identified. Then BPA and MG were focused to explore the disrupting effects of environmental estrogens on the two GHRs. Through the method of real-time PCR, both compounds could attenuate the gene expression level of GHRs in seabream hepatocytes. Using the method of luciferase assay, the signal transduction of the two GHRs was found to be desensitized by both BPA and MG. === Two genomic contigs of putative growth hormone receptor (GHR) were identified in fugu and zebrafish genomes by in silico analysis, suggesting the presence of two GHR subtypes in a single teleost species. This hypothesis was tested by cloning the full-length cDNA sequence of a second GHR subtype from the black seabream in which the first GHR subtype has been previously reported. Phylogenetic analysis of known GHR sequences from various vertebrates revealed that fish GHRs cluster into two distinct clades, viz. GHR1 and GHR2. The biological activities of both GHR subtypes from seabream had been examined using the reporter transcription assays in cultured eukaryotic cells. It was demonstrated that both of them have differential signal transduction upon Spi 2.1, beta-casein and c-fos promoter activities. === by Jiao, Baowei. === "December 2006." === Adviser: Christopher H. K. Cheng. === Source: Dissertation Abstracts International, Volume: 68-09, Section: B, page: 5662. === Thesis (Ph.D.)--Chinese University of Hong Kong, 2006. === Includes bibliographical references (p. 150-180). === Electronic reproduction. Hong Kong : Chinese University of Hong Kong, [2012] System requirements: Adobe Acrobat Reader. Available via World Wide Web. === Electronic reproduction. [Ann Arbor, MI] : ProQuest Information and Learning, [200-] System requirements: Adobe Acrobat Reader. Available via World Wide Web. === Abstract in English and Chinese. === School code: 1307.
author2 Jaio, Baowei.
author_facet Jaio, Baowei.
title A novel growth hormone receptor subtype in black seabream: cDNA cloning, regulation of gene expression and its disruption by environmental estrogens.
title_short A novel growth hormone receptor subtype in black seabream: cDNA cloning, regulation of gene expression and its disruption by environmental estrogens.
title_full A novel growth hormone receptor subtype in black seabream: cDNA cloning, regulation of gene expression and its disruption by environmental estrogens.
title_fullStr A novel growth hormone receptor subtype in black seabream: cDNA cloning, regulation of gene expression and its disruption by environmental estrogens.
title_full_unstemmed A novel growth hormone receptor subtype in black seabream: cDNA cloning, regulation of gene expression and its disruption by environmental estrogens.
title_sort novel growth hormone receptor subtype in black seabream: cdna cloning, regulation of gene expression and its disruption by environmental estrogens.
publishDate 2006
url http://library.cuhk.edu.hk/record=b6074207
http://repository.lib.cuhk.edu.hk/en/item/cuhk-343836
_version_ 1718978195951190016
spelling ndltd-cuhk.edu.hk-oai-cuhk-dr-cuhk_3438362019-02-19T03:44:05Z A novel growth hormone receptor subtype in black seabream: cDNA cloning, regulation of gene expression and its disruption by environmental estrogens. CUHK electronic theses & dissertations collection Cloning Estrogen Genetic regulation Somatotropin--Receptors Sparidae In the tissue distribution study, the expression of GHR2 is significantly higher than GHR1 in many tissues of the seabream including the gonad, kidney, muscle, pituitary and spleen. In vivo hormone treatment data indicated that cortisol and testosterone have differential expression regulation between GHR1 and GHR2. On the other hand, hepatic expression of both GHR1 and GHR2 in seabream was decreased by estradiol treatment. In primary cultures of seabream hepatocytes, the expression patterns after treatment by the various concentrations of hormones were consistent with the in vivo results. To study the actions of environmental estrogens on the somatotropic axis, a transgenic yeast system was developed for estrogenicity screening. The fish estrogen receptor (gfER) and a reporter vector containing the estrogen responsive element (ERE) were expressed in yeast cells as a means to identify potential estrogens. Using this system, more than fifty chemicals including pesticides, herbicides, industrial chemicals and phytoestrogens were screened. Ten compounds including dibutyl phthalate (DBP) and bisphenol A (BPA) were demonstrated to exhibit estrogenic activities. And a compound (malachite green, MG) with novel anti-estrogenenic activities was identified. Then BPA and MG were focused to explore the disrupting effects of environmental estrogens on the two GHRs. Through the method of real-time PCR, both compounds could attenuate the gene expression level of GHRs in seabream hepatocytes. Using the method of luciferase assay, the signal transduction of the two GHRs was found to be desensitized by both BPA and MG. Two genomic contigs of putative growth hormone receptor (GHR) were identified in fugu and zebrafish genomes by in silico analysis, suggesting the presence of two GHR subtypes in a single teleost species. This hypothesis was tested by cloning the full-length cDNA sequence of a second GHR subtype from the black seabream in which the first GHR subtype has been previously reported. Phylogenetic analysis of known GHR sequences from various vertebrates revealed that fish GHRs cluster into two distinct clades, viz. GHR1 and GHR2. The biological activities of both GHR subtypes from seabream had been examined using the reporter transcription assays in cultured eukaryotic cells. It was demonstrated that both of them have differential signal transduction upon Spi 2.1, beta-casein and c-fos promoter activities. by Jiao, Baowei. "December 2006." Adviser: Christopher H. K. Cheng. Source: Dissertation Abstracts International, Volume: 68-09, Section: B, page: 5662. Thesis (Ph.D.)--Chinese University of Hong Kong, 2006. Includes bibliographical references (p. 150-180). Electronic reproduction. Hong Kong : Chinese University of Hong Kong, [2012] System requirements: Adobe Acrobat Reader. Available via World Wide Web. Electronic reproduction. [Ann Arbor, MI] : ProQuest Information and Learning, [200-] System requirements: Adobe Acrobat Reader. Available via World Wide Web. Abstract in English and Chinese. School code: 1307. Jaio, Baowei. Chinese University of Hong Kong Graduate School. Division of Environmental Science. 2006 Text theses electronic resource microform microfiche 1 online resource (xvi, 180 p. : ill.) cuhk:343836 isbn: 9780549230908 http://library.cuhk.edu.hk/record=b6074207 eng chi Use of this resource is governed by the terms and conditions of the Creative Commons “Attribution-NonCommercial-NoDerivatives 4.0 International” License (http://creativecommons.org/licenses/by-nc-nd/4.0/) http://repository.lib.cuhk.edu.hk/en/islandora/object/cuhk%3A343836/datastream/TN/view/A%20%20novel%20growth%20hormone%20receptor%20subtype%20in%20black%20seabream%20%3A%20cDNA%20cloning%2C%20regulation%20of%20gene%20expression%20and%20its%20disruption%20by%20environmental%20estrogens.jpghttp://repository.lib.cuhk.edu.hk/en/item/cuhk-343836