Monoallelic expression of human PEG1/MEST is paralleled by parent- specific methylation in fetuses

Genomics

Volumn 42, Issue 2, 1997, Pages 236-244

  Riesewijk, Anne M ^a,b   Hu, Landian ^a   Schulz, Ute ^a   Tariverdian, Gholamali ^c   Höglund, Pia ^d   Kere, Jura ^d   Ropers, Hans Hilger ^a,b   Kalscheuer, Vera M ^a  

^a MAX PLANCK INSTITUTE FOR MOLECULAR GENETICS   (Germany)

^b RADBOUD UNIVERSITY MEDICAL CENTER   (Netherlands)

^c UNIVERSITY OF HEIDELBERG   (Germany)

^d UNIVERSITY OF HELSINKI   (Finland)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CHROMOSOME 3P; CHROMOSOME 5P; CHROMOSOME 7Q; FETUS; GENE ISOLATION; GENE MAPPING; GENE SEQUENCE; HUMAN; METHYLATION; PRIORITY JOURNAL;

EID: 0031172451     PISSN: 08887543     EISSN: None     Source Type: Journal    
DOI: 10.1006/geno.1997.4731     Document Type: Article

References (28)

1. Barlow, D. P., Stöger, R., Herrmann, B. G., Saito, K., and Schweifer, N. (1991). The mouse insulin-like growth factor type-2 receptor is imprinted and closely linked to the Tme locus. Nature 349: 84-87.
2. Beechey, C. V., and Cattanach, B. M. (1995). Genetic imprinting map. Mouse Genome 93: 89-91.
3. Cattanach, B. M., and Beechey, C. V. (1990). Autosomal and X-chromosome imprinting. Development Suppl.: 63-72.
4. Eggerding, F. A., Schonberg, S. A., Chehab, F. F., Norton, M. E., Cox, V. A., and Epstein, C. J. (1994). Uniparental disomy for paternal 7p and maternal 7q in a child with growth retardation. Am. J. Hum. Genet. 55: 253-265.
5. Ekström, T. J., Cui, H., Li, X., and Ohlsson, R. (1995). Promoter-specific IGF2 imprinting status and its plasticity during human liver development. Development 121: 309-316.
6. Höglund, P., Holmberg, C., de la Chapelle, A., and Kere, J. (1994). Paternal isodisomy for chromosome 7 is compatible with normal growth and development in a patient with congenital chloride diarrhea. Am. J. Hum. Genet. 55: 747-752.
7. Jinno, Y., Ikeda, Y., Yun, K., Maw, M., Masuzaki, H., Fukuda, H., Inuzuka, K., Fujishita, A., Ohtani, Y., Okimoto, T., Ishimaru, T., and Niikawa, N. (1995). Establishment of functional imprinting of the H19 gene in human developing placentae. Nature Genet 10: 318-324.
8. Kalscheuer, V. M., Mariman, E. C., Schepens, M. T., Rehder, H., and Ropers, H.-H. (1993). The insulin-like growth factor type-2 receptor gene is imprinted in the mouse but not in humans. Nature Genet. 5: 74-78.
9. Kaneko-Ishino, T., Kuroiwa, Y., Miyoshi, N., Kohda, T., Suzuki, R., Yokoyama, M., Viville, S., Barton, S. C., Ishino, F., and Surani, M. A. (1995). Peg1/Mest imprinted gene on chromosome 6 identified by cDNA subtraction hybridization. Nature Genet. 11: 52-59.
10. Kotzot, D., Schmitt, S., Bernasconi, F., Robinson, W. P., Lurie, I. W., Ilyina, H., Mehes, K., Hamel, B. C. J., Otten, B. J., Hergersberg, M., Werder, E., Schoenle, E., and Schinzel, A. (1995). Uniparental disomy 7 in Silver-Russell syndrome and primordial growth retardation. Genomics 4: 583-587.
11. Neumann, B., Kubicka, P., and Barlow, D. P. (1995). Characteristics of imprinted genes. Nature Genet. 9: 12-13.
12. Nishita, Y., Yoshida, I., Sado, T., and Takagi, N. (1996). Genomic imprinting and chromosomal localization of the human MEST gene. Genomics 36: 539-542.
13. Ogawa, O., McNoe, A., Eccles, M. R., Morison, I. M., and Reeve, A. E. (1993). Human insulin-like growth factor type I and type II receptors are not imprinted. Hum. Mol. Genet. 2: 2163-2165.
14. Ohlsson, R., Hedborg, F., Holmgren, L., Walsh, C., and Ekström, T. J. (1994). Overlapping patterns of IGF2 and H19 expression during human development: Biallelic IGF2 expression correlates with a lack of H19 expression. Development 120: 361-368.
15. Orita, M., Iwahana, H., Kanazawa, H., Hayashi, K., and Sekiya, T. (1989). Detection of polymorphisms of human DNA by gel electrophoresis as single-strand conformation polymorphisms. Proc. Natl. Acad. Sci. USA 86: 2766-2770.
16. Ferez Jurado, L. A., Peoples, R., Kaplan, P., Hamel, B. C. J., and Francke, U. (1996). Molecular definition of the chromosome 7 deletion in Williams syndrome and parent-of-origin effects on growth. Am. J. Hum. Genet. 59: 781-792.
17. Riesewijk, A. M., Schepens, M. T., Mariman, E. M., Ropers, H.-H., and Kalscheuer, V. M. (1996a). The MAS proto-oncogene is not imprinted in humans. Genomics 35: 380-382.
18. Riesewijk, A. M., Schepens, M. T., Welch, T. R., van den Berg-Loonen, E. M., Mariman, E., Ropers, H.-H., and Kalscheuer, V. M. (1996b). Maternal-specific methylation of the human IGF2R gene is not accompanied by allele-specific transcription. Genomics 31: 158-166.
19. Sado, T., Nakajima, N., Tada, M., and Takagi, N. (1993). A novel mesoderm-specific cDNA isolated from a mouse embryonal carcinoma cell line. Dev. Growth Differ. 35: 551-560.
20. Sambrook, J., Fritsch, E. F., and Maniatis, T. (1989) "Molecular Cloning: A Laboratory Manual," 2nd ed., Cold Spring Harbor Laboratory Press, Cold Spring Harbor, NY.
21. Spence, J. E., Perciaccante, R. G., Greig, G. M., Huntington, F. W., Ledbetter, D. H., Hejtmancik, J. F., Pollack, M. S., O'Brien, W. E., and Beaudet, A. L. (1989). Uniparental disomy as a mechnism for human genetic disease. Am. J. Hum. Genet. 42: 217-226.
22. Spotila, L. D., Sereda, L., and Prockop, D. J. (1992). Partial isodisomy for maternal chromosome 7 and short stature in an individual with a mutation at the COL1A2 locus. Am. J. Hum. Genet. 51: 1396-1405.
23. Suijkerbuijk, R. F., Meloni, A. M., Sinke, R. J., de Leeuw, B., Wilbrink, M., Janssen, H. A. P., Geraghty, M. T., Monaco, A. P., Sandberg, A. A., and Geurts van Kessel, A. (1993). Identification of a yeast artificial chromosome that spans the human papillary renal cell carcinoma-associated t(X;1) breakpoint in Xp11.2. Cancer Genet. Cytogenet. 71: 164-169.
24. Telenius, H., Carter, N. P., Bebb, C. E., Nordenskjöld, M., Ponder, B. A., and Tunnacliffe, A. (1992). Degenerate oligonucleotide-primed PCR: General amplification of target DNA by a single degenerate primer. Genomics 13: 718-725.
25. Tremblay, K. D., Saam, J. R., Ingram, R. S., Tilghman, S. M., and Bartolomei, M. S. (1995). A paternal-specific methylation imprint marks the alleles of the mouse H19 gene. Nature Genet. 9: 407-413.
26. Villar, A., and Pedersen, R. A. (1994). Parental imprinting of the Mas protooncogene in mouse. Nature Genet. 8: 373-379.
27. Voss, R., Ben-Simon, E., Avital, A., Godrey, S., Zlotogora, J., Daga, J., Tikochinski, Y., and Hillel, J. (1989). Isodisomy for chromosome 7 in a patient with cystic fibrosis: Could uniparental disomy be common in humans? Am. J. Hum. Genet. 45: 373-380.
28. Vu, T. H., and Hoffman, A. R. (1994). Promoter-specific imprinting of the human insulin-like growth factor-II gene. Nature 371: 714-717.