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Transcription of follicle-stimulating hormone subunit genes is modulated by porcine LIM homeobox transcription factors, LHX2 and LHX3

The LIM-homeobox transcription factors LHX2 and LHX3s (LHX3a and LHX3b) are thought to be involved in regulating the pituitary glycoprotein hormone subunit genes Cga and Fshβ. These two factors show considerable differences in their amino acid sequences for DNA binding and protein-protein interactio...

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Autores principales: YOSHIDA, Saishu, KATO, Takako, NISHIMURA, Naoto, KANNO, Naoko, CHEN, Mo, UEHARU, Hiroki, NISHIHARA, Hiroto, KATO, Yukio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Society for Reproduction and Development 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4919287/
https://www.ncbi.nlm.nih.gov/pubmed/26853788
http://dx.doi.org/10.1262/jrd.2015-163
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author YOSHIDA, Saishu
KATO, Takako
NISHIMURA, Naoto
KANNO, Naoko
CHEN, Mo
UEHARU, Hiroki
NISHIHARA, Hiroto
KATO, Yukio
author_facet YOSHIDA, Saishu
KATO, Takako
NISHIMURA, Naoto
KANNO, Naoko
CHEN, Mo
UEHARU, Hiroki
NISHIHARA, Hiroto
KATO, Yukio
author_sort YOSHIDA, Saishu
collection PubMed
description The LIM-homeobox transcription factors LHX2 and LHX3s (LHX3a and LHX3b) are thought to be involved in regulating the pituitary glycoprotein hormone subunit genes Cga and Fshβ. These two factors show considerable differences in their amino acid sequences for DNA binding and protein-protein interactions and in their vital function in pituitary development. Hence, we compared the DNA binding properties and transcriptional activities of Cga and Fshβ between LHX2 and LHX3s. A gel mobility shift assay for approximately 1.1 kb upstream of Cga and 2.0 kb upstream of Fshβ varied in binding profiles between LHX2 and LHX3s. DNase I footprinting revealed DNA binding sites in 8 regions of the Cga promoter for LHX2 and LHX3s with small differences in the binding range and strength. In the Fshβ promoter, 14 binding sites were identified for LHX2 and LHX3, respectively. There were alternative binding sites to either gene in addition to similar differences observed in the Cga promoter. The transcriptional activities of LHX2 and LHX3s according to a reporter assay showed cell-type dependent activity with repression in the pituitary gonadotrope lineage LβT2 cells and stimulation in Chinese hamster ovary lineage CHO cells. Reactivity of LHX2 and LHX3s was observed in all regions, and differences were observed in the 5'-upstream region of Fshβ. However, immunohistochemistry showed that LHX2 resides in a small number of gonadotropes in contrast to LHX3. Thus, LHX3 mainly controls Cga and Fshβ expression.
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spelling pubmed-49192872016-06-24 Transcription of follicle-stimulating hormone subunit genes is modulated by porcine LIM homeobox transcription factors, LHX2 and LHX3 YOSHIDA, Saishu KATO, Takako NISHIMURA, Naoto KANNO, Naoko CHEN, Mo UEHARU, Hiroki NISHIHARA, Hiroto KATO, Yukio J Reprod Dev Original Article The LIM-homeobox transcription factors LHX2 and LHX3s (LHX3a and LHX3b) are thought to be involved in regulating the pituitary glycoprotein hormone subunit genes Cga and Fshβ. These two factors show considerable differences in their amino acid sequences for DNA binding and protein-protein interactions and in their vital function in pituitary development. Hence, we compared the DNA binding properties and transcriptional activities of Cga and Fshβ between LHX2 and LHX3s. A gel mobility shift assay for approximately 1.1 kb upstream of Cga and 2.0 kb upstream of Fshβ varied in binding profiles between LHX2 and LHX3s. DNase I footprinting revealed DNA binding sites in 8 regions of the Cga promoter for LHX2 and LHX3s with small differences in the binding range and strength. In the Fshβ promoter, 14 binding sites were identified for LHX2 and LHX3, respectively. There were alternative binding sites to either gene in addition to similar differences observed in the Cga promoter. The transcriptional activities of LHX2 and LHX3s according to a reporter assay showed cell-type dependent activity with repression in the pituitary gonadotrope lineage LβT2 cells and stimulation in Chinese hamster ovary lineage CHO cells. Reactivity of LHX2 and LHX3s was observed in all regions, and differences were observed in the 5'-upstream region of Fshβ. However, immunohistochemistry showed that LHX2 resides in a small number of gonadotropes in contrast to LHX3. Thus, LHX3 mainly controls Cga and Fshβ expression. The Society for Reproduction and Development 2016-02-08 2016-06 /pmc/articles/PMC4919287/ /pubmed/26853788 http://dx.doi.org/10.1262/jrd.2015-163 Text en ©2016 Society for Reproduction and Development http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial No Derivatives (by-nc-nd) License.
spellingShingle Original Article
YOSHIDA, Saishu
KATO, Takako
NISHIMURA, Naoto
KANNO, Naoko
CHEN, Mo
UEHARU, Hiroki
NISHIHARA, Hiroto
KATO, Yukio
Transcription of follicle-stimulating hormone subunit genes is modulated by porcine LIM homeobox transcription factors, LHX2 and LHX3
title Transcription of follicle-stimulating hormone subunit genes is modulated by porcine LIM homeobox transcription factors, LHX2 and LHX3
title_full Transcription of follicle-stimulating hormone subunit genes is modulated by porcine LIM homeobox transcription factors, LHX2 and LHX3
title_fullStr Transcription of follicle-stimulating hormone subunit genes is modulated by porcine LIM homeobox transcription factors, LHX2 and LHX3
title_full_unstemmed Transcription of follicle-stimulating hormone subunit genes is modulated by porcine LIM homeobox transcription factors, LHX2 and LHX3
title_short Transcription of follicle-stimulating hormone subunit genes is modulated by porcine LIM homeobox transcription factors, LHX2 and LHX3
title_sort transcription of follicle-stimulating hormone subunit genes is modulated by porcine lim homeobox transcription factors, lhx2 and lhx3
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4919287/
https://www.ncbi.nlm.nih.gov/pubmed/26853788
http://dx.doi.org/10.1262/jrd.2015-163
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