EurekaMag.com logo
+ Site Statistics
References:
53,869,633
Abstracts:
29,686,251
+ Search Articles
+ Subscribe to Site Feeds
EurekaMag Most Shared ContentMost Shared
EurekaMag PDF Full Text ContentPDF Full Text
+ PDF Full Text
Request PDF Full TextRequest PDF Full Text
+ Follow Us
Follow on FacebookFollow on Facebook
Follow on TwitterFollow on Twitter
Follow on LinkedInFollow on LinkedIn

+ Translate

Paternal imprinting of mouse serotonin receptor 2A gene Htr2 in embryonic eye: a conserved imprinting regulation on the RB/Rb locus



Paternal imprinting of mouse serotonin receptor 2A gene Htr2 in embryonic eye: a conserved imprinting regulation on the RB/Rb locus



Genomics 47(1): 146-148



Parental allele-specific expression of the Htr2 gene was studied in tissues from reciprocal crosses between C57BL/6J and PWK mice using the Sph1 restriction site polymorphism between the 2 mouse strains. Expression of the Htr2 gene in the cerebrum and ovaries was demonstrated by reverse transcription(RT)-PCR analysis; digestion of the RT-PCR product showed it to be the maternal allele.

(PDF emailed within 0-6 h: $19.90)

Accession: 003225044

Download citation: RISBibTeXText

PMID: 9465310

DOI: 10.1006/geno.1997.5089



Related references

Genomic imprinting of the human serotonin-receptor (HTR2) gene involved in development of retinoblastoma. American Journal of Human Genetics 59(5): 1084-1090, 1996

A human imprinting centre demonstrates conserved acquisition but diverged maintenance of imprinting in a mouse model for Angelman syndrome imprinting defects. Human Molecular Genetics 15(3): 393-404, 2005

Genetic analysis of genomic imprinting: an Imprintor-1 gene controls inactivation of the paternal copy of the mouse Tme locus. Cell 70(3): 443-450, 1992

Imprinting on chromosome 20: tissue-specific imprinting and imprinting mutations in the GNAS locus. American Journal of Medical Genetics. Part C, Seminars in Medical Genetics 154c(3): 377-386, 2010

Interaction between the Xce locus and imprinting of the paternal X chromosome in mouse yolk-sac endoderm. Nature 303(5918): 635-637, 1983

Interaction between the Xce locus and imprinting of the paternal X chromosome in mouse yolk-sac endoderm. Nature, UK 303(5918): 635-637, 1983

DNA Methylation and Gene Regulation || Changes in DNA Methylation During Mouse Embryonic Development in Relation to X-Chromosome Activity and Imprinting. Philosophical Transactions of the Royal Society of London Series B Biological Sciences 326(1235): 299-312, 1990

Asymmetric regulation of imprinting on the maternal and paternal chromosomes at the Dlk1-Gtl2 imprinted cluster on mouse chromosome 12. Nature Genetics 35(1): 97-102, 2003

The serotonin receptor subtype 2 locus HTR2 is on human chromosome 13 near genes for esterase D and retinoblastoma-1 and on mouse chromosome 14. Somatic Cell and Molecular Genetics 16(6): 567-574, 1990

The molecular basis of imprinting the mouse and human Igf2/M6p receptor locus. Chromosome Research 3(SUPPL 1): 12-13, 1995

Characterization and imprinting status of OBPH1/Obph1 gene: Implications for an extended imprinting domain in human and mouse. Genomics 80(6): 575-584, December, 2002

Domain regulation of imprinting cluster in Kip2/Lit1 subdomain on mouse chromosome 7F4/F5: large-scale DNA methylation analysis reveals that DMR-Lit1 is a putative imprinting control region. Genome Research 12(12): 1860-1870, 2002

Domain regulation of imprinting cluster in Kip2/Lit1 subdomain on mouse chromosome 7F4/F5: large-scale DNA methylation analysis reveals that DMR-Lit1 is a putative imprinting control region. Genome Research 14(9): 1820-1820, 2004

Polymorphic imprinting of the serotonin-2A (5-HT2A) receptor gene in human adult brain. Molecular Brain Research 59(1): 90-92, 1998

Maternal imprinting of the mouse Snrpn gene and conserved linkage homology with the human Prader-Willi syndrome region. Nature Genetics 2(4): 259-263, 1992