Abstract
The GNAS1 gene encodes the alpha subunit of the guanine nucleotide-binding protein Gs, which couples signaling through peptide hormone receptors to cAMP generation. GNAS1 mutations underlie the hormone resistance syndrome pseudohypoparathyroidism type Ia (PHP-Ia), so the maternal inheritance displayed by PHP-Ia has raised suspicions that GNAS1 is imprinted. Despite this suggestion, in most tissues Gsalpha is biallelically encoded. In contrast, the large G protein XLalphas, also encoded by GNAS1, is paternally derived. Because the inheritance of PHP-Ia predicts the existence of maternally, rather than paternally, expressed transcripts, we have investigated the allelic origin of other mRNAs derived from GNAS1. We find this gene to be remarkable in the complexity of its allele-specific regulation. Two upstream promoters, each associated with a large coding exon, lie only 11 kb apart, yet show opposite patterns of allele-specific methylation and monoallelic transcription. The more 5' of these exons encodes the neuroendocrine secretory protein NESP55, which is expressed exclusively from the maternal allele. The NESP55 exon is 11 kb 5' to the paternally expressed XLalphas exon. The transcripts from these two promoters both splice onto GNAS1 exon 2, yet share no coding sequences. Despite their structural unrelatedness, the encoded proteins, of opposite allelic origin, both have been implicated in regulated secretion in neuroendocrine tissues. Remarkably, maternally (NESP55), paternally (XLalphas), and biallelically (Gsalpha) derived proteins all are produced by different patterns of promoter use and alternative splicing of GNAS1, a gene showing simultaneous imprinting in both the paternal and maternal directions.
MeSH Terms
Alleles
Amino Acid Sequence
Animals
Base Sequence
Cattle
Cloning, Molecular
DNA/chemistry,genetics
DNA Methylation
Exons
Eye/embryology,metabolism
Female
Fetus
GTP-Binding Protein alpha Subunits, Gs/biosynthesis,chemistry,genetics
Genomic Imprinting
Humans
Kidney/embryology,metabolism
Male
Mice
Molecular Sequence Data
Muscle, Skeletal/embryology,metabolism
Oncogene Proteins/genetics
Organ Specificity
Pseudohypoparathyroidism/genetics
Recombinant Proteins/biosynthesis,chemistry
Reverse Transcriptase Polymerase Chain Reaction
Sequence Alignment
Sequence Homology, Amino Acid
Chemicals
Oncogene Proteins
Recombinant Proteins
DNA
GTP-Binding Protein alpha Subunits, Gs
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Hayward B E
Human Genetics Unit, University of Edinburgh, Western General Hospital, Edinburgh EH4 2XU, United Kingdom.
Moran V
Strain L
Bonthron D T
References (23)
23 references, click to expand
-
Clinical and biological heterogeneity in pseudohypoparathyroidism syndrome. Results of a multicenter study.
Horm Res. 1997;48(3):120-30
PMID: 11546929
-
The gene responsible for pseudohypoparathyroidism type Ib is paternally imprinted and maps in four unrelated kindreds to chromosome 20q13.3.
Proc Natl Acad Sci U S A. 1998 Sep 29;95(20):11798-803
PMID: 9751745
-
Genetic deficiency of the alpha subunit of the guanine nucleotide-binding protein Gs as the molecular basis for Albright hereditary osteodystrophy.
Proc Natl Acad Sci U S A. 1988 Jan;85(2):617-21
PMID: 2829196
-
Isolation and characterization of the human Gs alpha gene.
Proc Natl Acad Sci U S A. 1988 Apr;85(7):2081-5
PMID: 3127824
-
Mutation in the gene encoding the stimulatory G protein of adenylate cyclase in Albright's hereditary osteodystrophy.
N Engl J Med. 1990 May 17;322(20):1412-9
PMID: 2109828
-
Alternative promoter and 5' exon generate a novel Gs alpha mRNA.
J Biol Chem. 1990 May 25;265(15):8458-62
PMID: 2111318
-
Mutations of the Gs alpha-subunit gene in Albright hereditary osteodystrophy detected by denaturing gradient gel electrophoresis.
Proc Natl Acad Sci U S A. 1990 Nov;87(21):8287-90
PMID: 2122458
-
Genetic mapping of the Gs-alpha subunit gene (GNAS1) to the distal long arm of chromosome 20 using a polymorphism detected by denaturing gradient gel electrophoresis.
Genomics. 1991 Apr;9(4):782-3
PMID: 1674732
-
Endocrine and molecular biological studies in a German family with Albright hereditary osteodystrophy.
Eur J Pediatr. 1993 Mar;152(3):185-9
PMID: 8444241
-
Imprinting in Albright's hereditary osteodystrophy.
J Med Genet. 1993 Feb;30(2):101-3
PMID: 8383205
-
Clonal insulinoma cell line that stably maintains correct glucose responsiveness.
Diabetes. 1994 Dec;43(12):1413-7
PMID: 7958492
-
XL alpha s is a new type of G protein.
Nature. 1994 Dec 22-29;372(6508):804-9
PMID: 7997272
-
Parental origin of transcription from the human GNAS1 gene.
J Med Genet. 1994 Aug;31(8):607-14
PMID: 7815417
-
Parental origin of Gs alpha gene mutations in Albright's hereditary osteodystrophy.
J Med Genet. 1994 Nov;31(11):835-9
PMID: 7853365
-
A human parthenogenetic chimaera.
Nat Genet. 1995 Oct;11(2):164-9
PMID: 7550344
-
Glomerular-specific imprinting of the mouse gsalpha gene: how does this relate to hormone resistance in albright hereditary osteodystrophy?
Genomics. 1996 Sep 1;36(2):280-7
PMID: 8812454
-
Molecular cloning and characterization of NESP55, a novel chromogranin-like precursor of a peptide with 5-HT1B receptor antagonist activity.
J Biol Chem. 1997 Apr 25;272(17):11657-62
PMID: 9111083
-
Imprinted expression of the Igf2r gene depends on an intronic CpG island.
Nature. 1997 Oct 16;389(6652):745-9
PMID: 9338788
-
Organization of the human glucokinase regulator gene GCKR.
Genomics. 1998 Apr 1;49(1):137-42
PMID: 9570959
-
Pseudohypoparathyroidism type Ia from maternal but not paternal transmission of a Gsalpha gene mutation.
Am J Med Genet. 1998 May 26;77(4):261-7
PMID: 9600732
-
Variable and tissue-specific hormone resistance in heterotrimeric Gs protein alpha-subunit (Gsalpha) knockout mice is due to tissue-specific imprinting of the gsalpha gene.
Proc Natl Acad Sci U S A. 1998 Jul 21;95(15):8715-20
PMID: 9671744
-
The human GNAS1 gene is imprinted and encodes distinct paternally and biallelically expressed G proteins.
Proc Natl Acad Sci U S A. 1998 Aug 18;95(17):10038-43
PMID: 9707596
-
Activity of the stimulatory guanine nucleotide-binding protein is reduced in erythrocytes from patients with pseudohypoparathyroidism and pseudopseudohypoparathyroidism: biochemical, endocrine, and genetic analysis of Albright's hereditary osteodystrophy in six kindreds.
J Clin Endocrinol Metab. 1986 Mar;62(3):497-502
PMID: 3003142