Genetic and functional analysis of neuronatin in mice with maternal or paternal duplication of distal Chr 2

Developmental Biology

Volumn 190, Issue 1, 1997, Pages 66-77

  Kikyo, Nobuaki ^a,c   Williamson, Christine M ^b   John, Rosalind M ^a   Barton, Sheila C ^a   Beechey, Colin V ^b   Ball, Simon T ^b   Cattanach, Bruce M ^b   Surani, M Azim ^a   Peters, Josephine ^b  

^a UNIVERSITY OF CAMBRIDGE   (United Kingdom)

^b MRC MAMMALIAN GENETICS UNIT   (United Kingdom)

^c NATIONAL INSTITUTES OF HEALTH   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CHROMOSOME 2; CHROMOSOME DUPLICATION; EMBRYO; EMBRYO DEVELOPMENT; FATHER; FEMALE; GENE EXPRESSION; GENETIC ANALYSIS; MALE; MOTHER; MOUSE; NONHUMAN; PRIORITY JOURNAL;

EID: 0031259754     PISSN: 00121606     EISSN: None     Source Type: Journal    
DOI: 10.1006/dbio.1997.8681     Document Type: Article

References (42)

1. Allen N. D., Logan K., Lally G., Drage D. J., Norris M. L., Keverne E. B. Distribution of parthenogenetic cells in the mouse brain and their influence on brain development and behavior. Proc. Natl. Acad. Sci. USA. 92:1995;10782-10786.
2. Bartolomei M. S., Webber A. L., Brunkow M. E., Tilghman S. M. Epigenetic mechanisms underlying the imprinting of the mouseH19. Genes Dev. 7:1993;1663-1673.
3. Barton S. C., Norris M. L., Surani M. A. H. Nuclear transplantation in fertilized and parthenogenetically activated eggs. Mammalian Development, A Practical Approach. 1987;IRL Press, Oxford. p. 235-253.
4. Barton S. C., Surani M. A. Manipulations of genetic constitution by nuclear transplantation. Wassarman P. M., DePamphilis M. L. Methods in Enzymology. 1993;732-744 Academic Press, San Diego.
5. Beechey C. V., Cattanach B. M. Genetic and physical imprinting map of the mouse. Mouse Genome. 95:1997;100-105.
6. Brenton J. D., Viville S., Surani M. A. Genomic imprinting and cancer. Ponder B. A. J., Cavenee W. K., Solomon E. Cancer Surveys, Genetics and Cancer: A Second Look. 1995;161-171 Cold Spring Harbor Laboratory Press, Cold Spring Harbor.
7. Buiting K., Saitoh S., Gross S., Dittrich B., Schwartz S., Nicholls R. D., Horsthemke B. Inherited microdeletions in the Angelman and Prader-Willi syndromes define an imprinting centre on human chromosome 15. Nat. Genet. 9:1995;395-400.
8. Carpenter M. B. Core Text of Neuroanatomy. 1991;Williams and Wilkins, Baltimore.
9. Cattanach B. M. Parental origin effects in mice. J. Embryol. Exp. Morphol. 97:1986;137-150.
10. Cattanach B. M., Beechey C. V. Reassessment of the proximal Chr 2 imprinting lethality. Mouse Genome. 93:1995;858-859.
11. Cattanach B. M., Evans E. P., Burtenshaw M., Beechey C. V. Further delimitation of the distal chromosome 2 imprinting region. Mouse Genome. 90:1992;82.
12. Cattanach B. M., Jones J. Genetic imprinting in the mouse; implications for gene regulation. J. Inher. Metab. Dis. 17:1994;403-420.
13. Cattanach B. M., Kirk M. Differential activity of maternally and paternally derived chromosome regions in mice. Nature. 315:1985;496-498.
14. Chomczynski P., Sacchi N. Single-step method of RNA isolation by acid guanidinium thiocyanate-phenol-chloroform extraction. Anal. Biochem. 162:1987;156-159.
15. de Boer P., van Gijsen M. The location of the positions of the breakpoints involved in the T26H and T70H mouse translocations with the aid of Giemsa-banding. Can. J. Genet. Cytol. 16:1974;783-788.
16. Dou D., Joseph R. Cloning of humanneuronatin. Brain Res. 723:1996;8-22.
17. Evans E. P. Karyotyping and sexing of gametes, embryos and fetuses and in situ hybridization to chromosomes. Monk M. Mammalian Development: A Practical Approach. 1987;93-114 IRL Press, Oxford.
18. Ferguson-Smith A. C., Sasaki H., Cattanach B. M., Surani M. A. Parental-origin-specific epigenetic modification of the mouseH19. Nature. 362:1993;751-755.
19. Fundele R. H., Surani M. A. Experimental embryological analysis of genetic imprinting in mouse development. Dev. Genet. 15:1994;515-522.
20. Gage F. H., Ray J., Fisher L. J. Isolation, characterization, and use of stem cells from the CNS. Annu. Rev. Neurosci. 18:1995;159-192.
21. Gold J. D., Pedersen R. A. Mechanisms of genomic imprinting in mammals. Curr. Top. Dev. Biol. 29:1994;227-280.
22. Hayashizaki Y., Shibata H., Hirotsune S., Sugino H., Okazaki Y., Sasaki N., Hirose K., Imoto H., Okuizumi H., Muramatsu M., Komatsubara H., Shiroishi T., Moriwaki K., Katsuki M., Hatano N., Sasaki H., Ueda T., Mise N., Takagi N., Plass C., Chapman V. M. Identification of an imprinted U2af binding protein related sequence on mouse chromosome 11 using the RLGS method. Nat. Genet. 6:1994;33-40.
23. Joseph R., Dou D., Tsang W. Molecular cloning of a novel mRNA (neuronatin) that is highly expressed in neonatal mammalian brain. Biochem. Biophys. Res. Commun. 201:1994;1227-1234.
24. Kagitani F., Kuroiwa Y., Wakana S., Shiroishi T., Miyoshi N., Kobayashi S., Nishida M., Kohda T., Kaneko-Ishino T., Ishino F. Peg5/Neuronatin. Nucleic Acids Res. 1997.
25. Kaneko-Ishino T., Kuroiwa Y., Miyoshi N., Kohda T., Suzuki R., Yokoyama M., Viville S., Barton S. C., Ishino F., Surani M. A. Peg1/Mest. Nat. Genet. 11:1995;52-59.
26. Keverne E. B. Olfactory learning. Curr. Opin. Neurobiol. 5:1995;482-488.
27. Keverne E. B., Fundele R., Narasimha M., Barton S. C., Surani M. A. Genomic imprinting and the differential roles of parental genomes in brain development. Dev. Brain Res. 92:1996;91-100.
28. Konecki D. S., Brennand J., Fuscoe J. C., Caskey C. T., Chinault A. C. Hypoxanthine-guanine phosphoribosyltransferase genes of the mouse and Chinese hamster: Construction and sequence analysis of cDNA recombinants. Nucleic Acids Res. 10:1982;6763-6775.
29. Kuroiwa Y., Kaneko-Ishino T., Kagitani F., Kohda T., Li L.-L., Tada M., Suzuki R., Yokoyama M., Shiroishi T., Wakana S., Barton S. C., Ishino F., Surani M. A. Peg3. Nat. Genet. 12:1996;186-190.
30. Latham K. E., McGrath J., Solter D. Mechanistic and developmental aspects of genetic imprinting in mammals. Int. Rev. Cytol. 160:1995;53-98.
31. Ledbetter D. H., Engel E. Uniparental disomy in humans: Development of an imprinting map and its implications for prenatal diagnosis. Hum. Mol. Genet. 4:1995;1757-1764.
32. Leighton P. A., Ingram R. S., Eggenschwiler J., Efstratiadis A., Tilghman S. M. Disruption of imprinting caused by deletion of theH19. Nature. 375:1995;34-39.
33. Liang P., Bauer D., Averboukh L., Warthoe P., Rohrwild M., Muller H., Strauss M., Pardee A. B. Analysis of altered gene expression by differential display. Vogt P. K., Verma I. M. Methods in Enzymology. 1995;304-321 Academic Press, San Diego.
34. Plumb M., Stein J., Stein G. Coordinate regulation of multiple histone mRNAs during the cell cycle in HeLa cells. Nucleic Acids Res. 11:1983;2391-2410.
35. Sambrook J., Fritsch E. F., Maniatis T. Molecular Cloning: A Laboratory Manual. 1989;Cold Spring Harbor Laboratory Press, New York.
36. Sasaki H., Jones P. A., Chaillet J. R., Ferguson-Smith A. C., Barton S. C., Reik W., Surani M. A. Parental imprinting: Potentially active chromatin of the repressed maternal allele of the mouse insulin-like growth factor II (Igf2. Genes Dev. 6:1992;1843-1856.
37. Searle A. G., Beechey C. V. Complementation studies with mouse translocations. Cytogenet. Cell. Genet. 20:1978;282-303.
38. Searle A. G., Ford C. E., Beechey C. V. Meiotic disjunction in mouse translocations and the determination of centromere position. Genet. Res. 18:1971;215-235.
39. Stöger R., Kubicka P., Liu C.-G., Kafri T., Razin A., Ceder H., Barlow D. P. Maternal-specific methylation of the imprinted mouseIgf2r. Cell. 73:1993;61-71.
40. Wijnholds J., Chowdhury K., Wehr R., Gruss P. Segment-specific expression of theneuronatin. Dev. Biol. 171:1995;73-84.
41. Wilkinson D. G., Nieto M. A. Detection of messenger RNA byin situ. Wassarman P. M., DePamphilis M. L. Methods in Enzymology. 1993;361-373 Academic Press, San Diego.
42. Williamson C. M., Miller H. J., Beechey C. V., Peters J. Microsatellite markerD2Mit226. Mouse Genome. 93:1995;860.