Gαopotentiates estrogen receptor α activity via the ERK signaling pathway

Melyssa R. Bratton; James WAntoon; Bich N. Duong; Daniel E. Frigo; Syreeta Tilghman; Bridgette M. Collins-Burow; Steven Elliott; Yan Tang; Lilia I. Melnik; Ling Lai; Jawed Alam; Barbara S. Beckman; Steven M. Hill; Brian G. Rowan; John A. McLachlan; Matthew E. Burow

doi:10.1530/JOE-12-0097

Gα_opotentiates estrogen receptor α activity via the ERK signaling pathway

Melyssa R. Bratton, James WAntoon, Bich N. Duong, Daniel E. Frigo, Syreeta Tilghman, Bridgette M. Collins-Burow, Steven Elliott, Yan Tang, Lilia I. Melnik, Ling Lai, Jawed Alam, Barbara S. Beckman, Steven M. Hill, Brian G. Rowan, John A. McLachlan, Matthew E. Burow

Research Institute

Research output: Contribution to journal › Article › peer-review

16 Scopus citations

Abstract

The estrogen receptor α (ERα) is a transcription factor that mediates the biological effects of 17β-estradiol (E2). ERa transcriptional activity is also regulated by cytoplasmic signaling cascades. Here, several Ga protein subunits were tested for their ability to regulate ERα activity. Reporter assays revealed that overexpression of a constitutively active Gα protein subunit potentiated ERα activity in the absence and presence of E2. Transient transfection of the human breast cancer cell line MCF-7 showed that Gα_o augments the transcription of several ERα-regulated genes. Western blots of HEK293T cells transfected with ERGGa_o revealed that Gao stimulated phosphorylation of ERK 1/2 and subsequently increased the phosphorylation of ERα on serine 118. In summary, our results show that Gα_o, through activation of the MAPK pathway, plays a role in the regulation of ERα activity.

Original language	English (US)
Pages (from-to)	45-54
Number of pages	10
Journal	Journal of Endocrinology
Volume	214
Issue number	1
DOIs	https://doi.org/10.1530/JOE-12-0097
State	Published - Jul 2012

ASJC Scopus subject areas

Endocrinology, Diabetes and Metabolism
Endocrinology

Access to Document

10.1530/JOE-12-0097

Cite this

Bratton, M. R., WAntoon, J., Duong, B. N., Frigo, D. E., Tilghman, S., Collins-Burow, B. M., Elliott, S., Tang, Y., Melnik, L. I., Lai, L., Alam, J., Beckman, B. S., Hill, S. M., Rowan, B. G., McLachlan, J. A., & Burow, M. E. (2012). Gα_opotentiates estrogen receptor α activity via the ERK signaling pathway. Journal of Endocrinology, 214(1), 45-54. https://doi.org/10.1530/JOE-12-0097

@article{c73a37db9db84f3792a2d99dfe1fede4,

title = "Gαopotentiates estrogen receptor α activity via the ERK signaling pathway",

abstract = "The estrogen receptor α (ERα) is a transcription factor that mediates the biological effects of 17β-estradiol (E2). ERa transcriptional activity is also regulated by cytoplasmic signaling cascades. Here, several Ga protein subunits were tested for their ability to regulate ERα activity. Reporter assays revealed that overexpression of a constitutively active Gα protein subunit potentiated ERα activity in the absence and presence of E2. Transient transfection of the human breast cancer cell line MCF-7 showed that Gαo augments the transcription of several ERα-regulated genes. Western blots of HEK293T cells transfected with ERGGao revealed that Gao stimulated phosphorylation of ERK 1/2 and subsequently increased the phosphorylation of ERα on serine 118. In summary, our results show that Gαo, through activation of the MAPK pathway, plays a role in the regulation of ERα activity.",

author = "Bratton, {Melyssa R.} and James WAntoon and Duong, {Bich N.} and Frigo, {Daniel E.} and Syreeta Tilghman and Collins-Burow, {Bridgette M.} and Steven Elliott and Yan Tang and Melnik, {Lilia I.} and Ling Lai and Jawed Alam and Beckman, {Barbara S.} and Hill, {Steven M.} and Rowan, {Brian G.} and McLachlan, {John A.} and Burow, {Matthew E.}",

year = "2012",

month = jul,

doi = "10.1530/JOE-12-0097",

language = "English (US)",

volume = "214",

pages = "45--54",

journal = "Journal of Endocrinology",

issn = "0022-0795",

publisher = "Society for Endocrinology",

number = "1",

}

TY - JOUR

T1 - Gαopotentiates estrogen receptor α activity via the ERK signaling pathway

AU - Bratton, Melyssa R.

AU - WAntoon, James

AU - Duong, Bich N.

AU - Frigo, Daniel E.

AU - Tilghman, Syreeta

AU - Collins-Burow, Bridgette M.

AU - Elliott, Steven

AU - Tang, Yan

AU - Melnik, Lilia I.

AU - Lai, Ling

AU - Alam, Jawed

AU - Beckman, Barbara S.

AU - Hill, Steven M.

AU - Rowan, Brian G.

AU - McLachlan, John A.

AU - Burow, Matthew E.

PY - 2012/7

Y1 - 2012/7

N2 - The estrogen receptor α (ERα) is a transcription factor that mediates the biological effects of 17β-estradiol (E2). ERa transcriptional activity is also regulated by cytoplasmic signaling cascades. Here, several Ga protein subunits were tested for their ability to regulate ERα activity. Reporter assays revealed that overexpression of a constitutively active Gα protein subunit potentiated ERα activity in the absence and presence of E2. Transient transfection of the human breast cancer cell line MCF-7 showed that Gαo augments the transcription of several ERα-regulated genes. Western blots of HEK293T cells transfected with ERGGao revealed that Gao stimulated phosphorylation of ERK 1/2 and subsequently increased the phosphorylation of ERα on serine 118. In summary, our results show that Gαo, through activation of the MAPK pathway, plays a role in the regulation of ERα activity.

AB - The estrogen receptor α (ERα) is a transcription factor that mediates the biological effects of 17β-estradiol (E2). ERa transcriptional activity is also regulated by cytoplasmic signaling cascades. Here, several Ga protein subunits were tested for their ability to regulate ERα activity. Reporter assays revealed that overexpression of a constitutively active Gα protein subunit potentiated ERα activity in the absence and presence of E2. Transient transfection of the human breast cancer cell line MCF-7 showed that Gαo augments the transcription of several ERα-regulated genes. Western blots of HEK293T cells transfected with ERGGao revealed that Gao stimulated phosphorylation of ERK 1/2 and subsequently increased the phosphorylation of ERα on serine 118. In summary, our results show that Gαo, through activation of the MAPK pathway, plays a role in the regulation of ERα activity.

UR - http://www.scopus.com/inward/record.url?scp=84864311891&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=84864311891&partnerID=8YFLogxK

U2 - 10.1530/JOE-12-0097

DO - 10.1530/JOE-12-0097

M3 - Article

C2 - 22562654

AN - SCOPUS:84864311891

VL - 214

SP - 45

EP - 54

JO - Journal of Endocrinology

JF - Journal of Endocrinology

SN - 0022-0795

IS - 1

ER -

Gα_opotentiates estrogen receptor α activity via the ERK signaling pathway

Abstract

ASJC Scopus subject areas

Access to Document

Other files and links

Fingerprint

Cite this