Luteinizing hormone-like and follicle-stimulating hormone-like activities of equine chorionic gonadotropin β-subunit mutants in cells expressing rat luteinizing hormone/chorionic gonadotropin receptor and rat follicle-stimulating hormone receptor.

CHO-S cells cAMP assay eCG rFSHR rLH/CGR

Journal

Animal cells and systems
ISSN: 1976-8354
Titre abrégé: Anim Cells Syst (Seoul)
Pays: England
ID NLM: 101478641

Informations de publication

Date de publication:
2021
Historique:
entrez: 15 7 2021
pubmed: 16 7 2021
medline: 16 7 2021
Statut: epublish

Résumé

To identify the specific region of eCG involved in FSH-like activity, the following mutant expression vectors were constructed targeting the amino acid residues 102-104 of the eCG β-subunit: single mutants, eCGβV102G/α, eCGβF103P/α, and eCGβR104K/α; double mutants, eCGβV102G;F103P/α, eCGβV102G;R104K/α, and eCGβF103P;R104K/α; triple mutant, eCGβV102G;F103P;R104K/α. The LH-like and FSH-like activities of eCG mutants were examined in CHO-K1 cells expressing rat LH/CG receptor and rat FSH receptor. The levels of eCGβV102G/α, eCGβR104K/α, and eCGβV102G;R104K/α in the culture supernatant were markedly lower than those of eCGβ/α-wt. The other mutants and rec-eCGβ/α-wt were efficiently secreted into the culture supernatant. The LH-like activities of eCGV104G/α, eCGβV102G;R104K/α, and eCGβF103P;R104K/α were approximately 61%, 52%, and 54%, respectively, of those of eCG-wt. The Rmax values of the mutants were 58.9%-78.8% those of eCG-wt with eCGβR104K/α exhibiting the lowest value. The FSH-like activities of single mutants were only 16%-20% of those of eCG-wt. Additionally, the FSH-like activity of double mutants was less than 10% of that of eCG-wt. In particular, the FSH-like activities of βV102G;R104K/α and βF103P;R104K/α were 2.5-2.9% of that of eCG-wt. These results suggest that the amino acid residues 102-104 of the eCG β-subunit are dispensable and that the residue 104 of the eCG β-subunit plays a pivotal role in signal transduction through the rat FSH receptor. Thus, these mutants may aid future studies on eCG interactions with mammalian FSH receptors

Identifiants

pubmed: 34262660
doi: 10.1080/19768354.2021.1943708
pii: 1943708
pmc: PMC8253215
doi:

Types de publication

Journal Article

Langues

eng

Pagination

171-181

Informations de copyright

© 2021 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group.

Déclaration de conflit d'intérêts

No potential conflict of interest was reported by the authors.

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Auteurs

Munkhzaya Byambaragchaa (M)

Animal Life and Environmental Science, Institute of Genetic Engineering, Hankyong National University, Ansung, Korea.

Ayoung Park (A)

Animal Life and Environmental Science, Institute of Genetic Engineering, Hankyong National University, Ansung, Korea.

So-Jin Gil (SJ)

School of Animal Life Biotechnology, Hankyong National University, Ansung, Korea.

Hae-Won Lee (HW)

School of Animal Life Biotechnology, Hankyong National University, Ansung, Korea.

Yun-Jeong Ko (YJ)

School of Animal Life Biotechnology, Hankyong National University, Ansung, Korea.

Seung-Hee Choi (SH)

Animal Life and Environmental Science, Institute of Genetic Engineering, Hankyong National University, Ansung, Korea.

Myung-Hwa Kang (MH)

Department of Food Science and Nutrition, Hoseo University, Asan, Korea.

Kwan-Sik Min (KS)

Animal Life and Environmental Science, Institute of Genetic Engineering, Hankyong National University, Ansung, Korea.
School of Animal Life Biotechnology, Hankyong National University, Ansung, Korea.

Classifications MeSH