» Articles » PMID: 10751211

Variable Imprinting of the Heterotrimeric G Protein G(s) Alpha-subunit Within Different Segments of the Nephron

Overview
Specialties Nephrology
Physiology
Date 2000 Apr 6
PMID 10751211
Citations 22
Authors
Affiliations
Soon will be listed here.
Abstract

The heterotrimeric G protein G(s) is required for hormone-stimulated intracellular cAMP generation because it couples hormone receptors to the enzyme adenylyl cyclase. Hormones that activate G(s) in the kidney include parathyroid hormone, glucagon, calcitonin, and vasopressin. Recently, it has been demonstrated that the G(s)alpha gene is imprinted in a tissue-specific manner, leading to preferential expression of G(s)alpha from the maternal allele in some tissues. In the kidney, G(s)alpha is imprinted in the proximal tubule but not in more distal nephron segments, such as the thick ascending limb or collecting duct. This most likely explains why in both humans and mice heterozygous mutations in the maternal allele lead to parathyroid hormone resistance in the proximal tubule whereas mutations in the paternal allele do not. In contrast, heterozygous mutations have little effect on vasopressin action in the collecting ducts. In mice with heterozygous null G(s)alpha mutations (both those with mutations on the maternal or paternal allele), expression of the Na-K-2Cl cotransporter was decreased in the thick ascending limb, suggesting that its expression is regulated by cAMP. The G(s)alpha genes also generate alternative, oppositely imprinted transcripts encoding XLalphas, a G(s)alpha isoform with a long NH(2)-terminal extension, and NESP55, a chromogranin-like neurosecretory protein. The role, if any, of these proteins in renal physiology is unknown.

Citing Articles

Recurrent small variants in NESP55/NESPAS associated with broad GNAS methylation defects and pseudohypoparathyroidism type 1B.

Li D, De Beur S, Hou C, Ruzhnikov M, Seeley H, Cutting G JCI Insight. 2024; 9(24).

PMID: 39541438 PMC: 11665564. DOI: 10.1172/jci.insight.185874.


Hair follicle-resident progenitor cells are a major cellular contributor to heterotopic subcutaneous ossifications in a mouse model of Albright hereditary osteodystrophy.

McMullan P, Maye P, Root S, Yang Q, Edie S, Rowe D bioRxiv. 2024; .

PMID: 38948860 PMC: 11213030. DOI: 10.1101/2024.06.18.599506.


Pseudohypoparathyroidism: complex disease variants with unfortunate names.

Juppner H J Mol Endocrinol. 2023; 72(1).

PMID: 37965945 PMC: 10843601. DOI: 10.1530/JME-23-0104.


Prevalence of Chiari malformation type 1 is increased in pseudohypoparathyroidism type 1A and associated with aberrant bone development.

Krishnan N, McMullan P, Yang Q, Buscarello A, Germain-Lee E PLoS One. 2023; 18(1):e0280463.

PMID: 36662765 PMC: 9858345. DOI: 10.1371/journal.pone.0280463.


Parental Origin of Inactivation Differentially Affects Bone Remodeling in a Mouse Model of Albright Hereditary Osteodystrophy.

McMullan P, Maye P, Yang Q, Rowe D, Germain-Lee E JBMR Plus. 2022; 6(1):e10570.

PMID: 35079678 PMC: 8771002. DOI: 10.1002/jbm4.10570.