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

Research output: Contribution to journalArticle

7 Citations (Scopus)

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.

Original languageEnglish (US)
Pages (from-to)355-360
Number of pages6
JournalClinical and translational science
Volume2
Issue number5
StatePublished - Oct 2009
Externally publishedYes

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Cell culture
Cell Culture Techniques
Alleles
Cells
Tissue
Mothers
Proteins
Exons
Genes
Polyostotic Fibrous Dysplasia
Genomic Imprinting
Embryonic Germ Cells
Germ Cells
Phenotype
Mutation

ASJC Scopus subject areas

  • Neuroscience(all)
  • Biochemistry, Genetics and Molecular Biology(all)
  • Pharmacology, Toxicology and Pharmaceutics(all)

Cite this

Imprinting status of Galpha(s), NESP55, and XLalphas in cell cultures derived from human embryonic germ cells : GNAS imprinting in human embryonic germ cells. / Crane, Janet L.; Shamblott, Michael J.; Axelman, Joyce; Hsu, Stephanie; Levine, Michael A.; Germain-Lee, Emily L.

In: Clinical and translational science, Vol. 2, No. 5, 10.2009, p. 355-360.

Research output: Contribution to journalArticle

Crane, Janet L. ; Shamblott, Michael J. ; Axelman, Joyce ; Hsu, Stephanie ; Levine, Michael A. ; Germain-Lee, Emily L. / Imprinting status of Galpha(s), NESP55, and XLalphas in cell cultures derived from human embryonic germ cells : GNAS imprinting in human embryonic germ cells. In: Clinical and translational science. 2009 ; Vol. 2, No. 5. pp. 355-360.
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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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