A new region of conservation is defined between human and mouse X chromosomes

Genomics

Volumn 35, Issue 1, 1996, Pages 244-247

  Dinulos, Mary Beth ^a   Bassi, Maria T ^b   Rugarli, Elena I ^c   Chapman, Verne ^d   Ballabio, Andrea ^b,c   Disteche, Christine M ^a  

^a UNIVERSITY OF WASHINGTON   (United States)

^b UNIVERSITY OF SIENA   (Italy)

^c TELETHON INSTITUTE OF GENETICS AND MEDICINE TIGEM   (Italy)

^d ROSWELL PARK CANCER INSTITUTE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ANIMAL CELL; ARTICLE; CHROMOSOME 7; CHROMOSOME MAP; CHROMOSOME REARRANGEMENT; EVOLUTION; HUMAN; HUMAN CELL; MOUSE; NONHUMAN; PRIORITY JOURNAL; X CHROMOSOME;

ANIMALIA; EUTHERIA; MAMMALIA; MURINAE; MUS SPRETUS; XENOPUS LAEVIS;

EID: 0030200922     PISSN: 08887543     EISSN: None     Source Type: Journal    
DOI: 10.1006/geno.1996.0347     Document Type: Article

References (17)

1. 1. Bassi, M. T., Schiaffino, M. V., Renieri, A., De Nigris, F., Galli, L., Bruttini, M., Gebbia, M., Bergen, A. A. B., Lewis, R. A., and Ballabio, A. (1995). Cloning of the gene for ocular albinism type 1 from the distal short arm of the X chromosome. Nature Genet. 10: 13-19.
2. 2. Blair, H. J., Reed, V., Laval, S. H., and Boyd, Y. (1994). New insights into the man-mouse comparative map of the X chromosome. Genomics 19: 215-220.
3. 3. Chapman, V. M., Keitz, B. T., and Bishop, D. F. (1994). Genetic linkage of the erythroid-specific delta-aminolevulinate synthase gene (Alas2) to the distal region of the mouse X chromosome. Mamm. Genome 5: 741.
4. 4. Cotter, P. D., Willard, H. F., Gorski, J. L., and Bishop, D. F. (1992). Assignment of human erythroid delta-aminolevulinate synthase (ALAS2) to a distal subregion of band Xp11.2 by PCR analysis of somatic cell hybrids containing X; autosome translocations. Genomics 13: 211-212.
5. 5. Disteche, C. M., Brannan, C. I., Larsen, A., Adler, D. A., Schorderet, D. F., Gearing, D., Copeland, N. G., Jenkins, N. A., and Park, L. S. (1992). The human pseudoautosomal GM-CSF receptor alpha subunit gene is autosomal in mouse. Nature Genet. 1: 333-336.
6. 6. Edelhoff, S., Ayer, D. E., Zervos, A. S., Steingrimsson, E., Jenkins, N. A., Copeland, N. G., Eisenman, R. N., Brent, R., and Disteche, C. M. (1994). Mapping of two genes encoding members of a distinct subfamily of MAX interacting proteins: MAD to human chromosome 2 and mouse chromosome 6, and MXII to human chromosome 10 and mouse chromosome 19. Oncogene 9: 665-668.
7. 7. Ferrero, G. B., Franco, B., Roth, E. J., Firulli, B. A., Borsani, G., Delmas-Mata, J., Weissenbach, J., Halley, G., Schlessinger, D., Chinault, A. C., Zoghbi, H. Y., Nelson, D. L., and Ballabio, A. (1995). An integrated physical and genetic map of a 35 Mb region on chromosome Xp22.3-Xp21.3. Hum. Mol. Genet. 4: 1821-1827.
8. 8. Keitges, E., Rivest, M., Siniscalco, M., and Gartler, S. M. (1985). X-linkage of steroid sulphatase in the mouse is evidence for a functional Y-linked allele. Nature 315: 226-227.
9. 9. Klink, A., Schiebel, K., Winkelmann, M., Rao, E., Horsthemke, B., Ludecke, H-J., Claussen, U., Scherer, G., and Rappold, G. (1995). The human protein kinase gene PKX1 on Xp22.3 displays Xp/Yp homology and is a site of chromosomal instability. Hum. Mol. Genet. 4: 869-878.
10. 10. Milatovich, A., Kitamura, T., Miyajima, A., and Francke, U. (1993). Gene for the α-subunit of the human interleukin-3 receptor (IL3RA) localized to the X-Y pseudoautosomal region. Am. J. Hum. Genet. 53: 1146-1153.
11. 11. Mullins, L. J., Grant, S. G., Stephenson, D. A., and Chapman, V. M. (1988). Multilocus molecular mapping of the mouse X chromosome. Genomics 3: 187-194.
12. 12. Ohno, S. (1967). "Sex Chromosomes and Sex-Linked Genes," Springer-Verlag, Berlin.
13. 13. Palmer, S., Perry, J., and Ashworth, A. (1995). A contravention of Ohno's law in mice. Nature Genet. 10: 472-476.
14. 14. Rugarli, E. I., Adler, D. A., Borsani, G., Tsuchiya, K., Franco, B., Hange, X., Disteche, C. M., Chapman, V., and Ballabio, A. (1995). Different chromosomal localization of the Clcn4 gene in Mus spretus and C57BL/6J mice. Nature Genet. 10: 466-471.
15. 15. Schiaffino, M. V., Bassi, M. T., Rugarli, E. I., Renieri, A., Galli, L., and Ballabio, A. (1995). Cloning of the human homologue of the Xenopus laevis APX gene from the ocular albinism type 1 critical region. Hum. Mol. Genet. 4: 373-382.
16. 16. van Slegtenhorst, M. A., Bassi, M. T., Borsani, G., Wapenaar, M. C., Ferrero, G. B., de Conciliis, L., Rugarli, E. I., Franco, B., Zoghbi, M. Y., and Ballabio, A. (1994). A gene from the Xp22.3 region shares homology with voltage-gated chloride channels. Hum. Mol. Genet. 3: 547-552.
17. 17. Yen, P. H., Allen, E., Marsh, B., Mohandas, T., Wang, N., Taggart, R. T., and Shapiro, L. J. (1987). Cloning and expression of steroid sulfatase cDNA and the frequent occurrence of deletions in STS deficiency: Implications for X-Y interchange. Cell 49: 443-445.