Literature DB >> 20443919

Imprinting status of Galpha(s), NESP55, and XLalphas in cell cultures derived from human embryonic germ cells: GNAS imprinting in human embryonic germ cells.

Janet L Crane1, Michael J Shamblott, Joyce Axelman, Stephanie Hsu, Michael A Levine, Emily L Germain-Lee.   

Abstract

GNAS is a complex gene that through use of alternative first exons encodes signaling proteins Galpha(s) and XLalphas plus neurosecretory protein NESP55. Tissue-specific expression of these proteins is regulated through reciprocal genomic imprinting in fully differentiated and developed tissue. Mutations in GNAS account for several human disorders, including McCune-Albright syndrome and Albright hereditary osteodystrophy, and further knowledge of GNAS imprinting may provide insights into variable phenotypes of these disorders. We therefore analyzed expression of Galpha(s), NESP55, and XLalphas prior to tissue differentiation in cell cultures derived from human primordia germ cells. We found that the expression of Galpha(s) was biallelic (maternal allele: 52.6%+/- 2.5%; paternal allele: 47.2%+/- 2.5%; p= 0.07), whereas NESP55 was expressed preferentially from the maternal allele (maternal allele: 81.9%+/- 10%; paternal allele: 18.1%+/- 10%; p= 0.002) and XLalphas was preferentially expressed from the paternal allele (maternal allele: 2.7%+/- 0.3%; paternal allele: 97.3%+/- 0.3%; p= 0.007). These results demonstrate that imprinting of NESP55 occurs very early in development, although complete imprinting appears to take place later than 5-11 weeks postfertilization, and that imprinting of XLalphas occurs very early postfertilization. By contrast, imprinting of Galpha(s) most likely occurs after 11 weeks postfertilization and after tissue differentiation.

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Year:  2009        PMID: 20443919      PMCID: PMC4434047          DOI: 10.1111/j.1752-8062.2009.00148.x

Source DB:  PubMed          Journal:  Clin Transl Sci        ISSN: 1752-8054            Impact factor:   4.689


  54 in total

1.  Genotyping with TaqMAMA.

Authors:  Baohui Li; Ibrahim Kadura; Dong-Jing Fu; David E Watson
Journal:  Genomics       Date:  2004-02       Impact factor: 5.736

2.  Discordance between genetic and epigenetic defects in pseudohypoparathyroidism type 1b revealed by inconsistent loss of maternal imprinting at GNAS1.

Authors:  Suzanne Jan de Beur; Changlin Ding; Emily Germain-Lee; Justin Cho; Alexander Maret; Michael A Levine
Journal:  Am J Hum Genet       Date:  2003-07-11       Impact factor: 11.025

Review 3.  Epigenetic reprogramming in mammals.

Authors:  Hugh D Morgan; Fátima Santos; Kelly Green; Wendy Dean; Wolf Reik
Journal:  Hum Mol Genet       Date:  2005-04-15       Impact factor: 6.150

Review 4.  GNAS locus and pseudohypoparathyroidism.

Authors:  Murat Bastepe; Harald Jüppner
Journal:  Horm Res       Date:  2005-02-09

5.  Bidirectional imprinting of a single gene: GNAS1 encodes maternally, paternally, and biallelically derived proteins.

Authors:  B E Hayward; V Moran; L Strain; D T Bonthron
Journal:  Proc Natl Acad Sci U S A       Date:  1998-12-22       Impact factor: 11.205

6.  Maternal methylation imprints on human chromosome 15 are established during or after fertilization.

Authors:  O El-Maarri; K Buiting; E G Peery; P M Kroisel; B Balaban; K Wagner; B Urman; J Heyd; C Lich; C I Brannan; J Walter; B Horsthemke
Journal:  Nat Genet       Date:  2001-03       Impact factor: 38.330

7.  Polymorphism of the gene encoding the alpha subunit of the stimulatory G-protein of adenylyl cyclase (GNAS1).

Authors:  C Waltman; M A Levine; W F Schwindinger; G S Wand
Journal:  Hum Genet       Date:  1994-04       Impact factor: 4.132

8.  A GNAS1 imprinting defect in pseudohypoparathyroidism type IB.

Authors:  J Liu; D Litman; M J Rosenberg; S Yu; L G Biesecker; L S Weinstein
Journal:  J Clin Invest       Date:  2000-11       Impact factor: 14.808

9.  The stimulatory G protein alpha-subunit Gs alpha is imprinted in human thyroid glands: implications for thyroid function in pseudohypoparathyroidism types 1A and 1B.

Authors:  Jie Liu; Beth Erlichman; Lee S Weinstein
Journal:  J Clin Endocrinol Metab       Date:  2003-09       Impact factor: 5.958

Review 10.  An epigenetic approach to cancer etiology.

Authors:  Andrew P Feinberg
Journal:  Cancer J       Date:  2007 Jan-Feb       Impact factor: 3.360

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  3 in total

1.  Paternal GNAS mutations lead to severe intrauterine growth retardation (IUGR) and provide evidence for a role of XLαs in fetal development.

Authors:  Nicolas Richard; Arnaud Molin; Nadia Coudray; Pauline Rault-Guillaume; Harald Jüppner; Marie-Laure Kottler
Journal:  J Clin Endocrinol Metab       Date:  2013-07-24       Impact factor: 5.958

2.  Syndromic Disorders Caused by Disturbed Human Imprinting

Authors:  Diana Carli; Evelise Riberi; Giovanni Battista Ferrero; Alessandro Mussa
Journal:  J Clin Res Pediatr Endocrinol       Date:  2019-04-10

3.  Methylation and transcripts expression at the imprinted GNAS locus in human embryonic and induced pluripotent stem cells and their derivatives.

Authors:  Virginie Grybek; Laetitia Aubry; Stéphanie Maupetit-Méhouas; Catherine Le Stunff; Cécile Denis; Mathilde Girard; Agnès Linglart; Caroline Silve
Journal:  Stem Cell Reports       Date:  2014-08-07       Impact factor: 7.765

  3 in total

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