Changes in chromosome positioning may contribute to the development of diseases related to X-chromosome aneuploidy

Journal of Cellular Physiology

Volumn 213, Issue 1, 2007, Pages 278-283

  Petrova, Natalia V ^a   Yakutenko, Irina I ^b   Alexeevski, Andrei V ^b   Verbovoy, Valentin A ^b   Razin, Sergey V ^a,b   Iarovaia, Olga V ^a  

^a INSTITUTE OF GENE BIOLOGY   (Russian Federation)

^b MOSCOW STATE UNIVERSITY   (Russian Federation)

Author keywords

[No Author keywords available]

Indexed keywords

ANEUPLOIDY; ARTICLE; CENTROMERE; CHROMOSOME 1; CHROMOSOME POSITIONING; COMPUTER ANALYSIS; CONTROLLED STUDY; FIBROBLAST; FLUORESCENCE IN SITU HYBRIDIZATION; GENOTYPE; HUMAN; HUMAN CELL; MALE; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; STATISTICAL ANALYSIS; X CHROMOSOME;

ANEUPLOIDY; CELLS, CULTURED; CENTROMERE; CHROMOSOMES, HUMAN, PAIR 1; CHROMOSOMES, HUMAN, X; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; MALE; SEX CHROMOSOME DISORDERS; X CHROMOSOME INACTIVATION;

EID: 34548475528     PISSN: 00219541     EISSN: None     Source Type: Journal    
DOI: 10.1002/jcp.21118     Document Type: Article

References (31)

1. Beyer V, Muhlematter D, Parlier V, Cabrol C, Bougeon-Mamin S, Solenthaler M, Tobler A, Pugin P, Gregor M, Hitz F, Hess U, Chapuis B, Laurencet F, Schanz U, Schmidt PM, van Melle G, Jotterand M. 2005. Polysomy 8 defines a clinico-cytogenetic entity representing a subset of myeloid hematologic malignancies associated with a poor prognosis: Report on a cohort of 12 patients and review of 105 published cases. Cancer Genet Cytogenet 160:97-119.
2. Bolzer A, Kreth G, Solovei I, Koehler D, Saracoglu K, Fauth C, Muller S, Eils R, Cremer C, Speicher MR, Cremer T. 2005. Three-dimensional maps of all chromosomes in human male fibroblast nuclei and prometaphase rosettes. PLoS Biol 3:e157.
3. Bourque G, Pevzner PA, 2002. Genome-scale evolution: Reconstructing gene orders in the ancestral species. Genome Res 12 26-36.
4. Boyle S, Gilchrist S, Bridger JM, Mahy NL, Ellis JA, Bickmore WA, 2001. The spatial organization of human chromosomes within the nuclei of normal and emerin-mutant cells. Human Mol Genet 10:211-219.
5. Brown CJ, Hendrich BD, Rupert JL, Lafreniere RG, Xing Y, Lawrence J, Willard HF, 1992. The human XIST gene: Analysis of a 17 kb inactive X-specific RNA that contains conserved repeats and is highly localized within the nucleus. Cell 71:527-542.
6. Cremer T, Cremer C, 2001. Chromosome territories, nuclear architecture and gene regulation in mammalian cells. Nat Rev Genet 2:292-301.
7. Cremer T, Kurz A, Zirbel R, Dietzel S, Rinke B, Schrock E, Speicher MR, Mathieu U, Jauch A, Emmerich P, Scherthan H, Ried T, Cremer C, Lichter P, 1993. Role of chromosome territories in the functional compartmentalization of the cell nucleus. Cold Spring Harb Symp Quant Biol 58:777-792.
8. Cremer T, Kreth G, Koester H, Fink RH, Heintzmann R, Cremer M, Solovei I, Zink D, Cremer C, 2000. Chromosome territories, interchromatin domain compartment, and nuclear matrix: An integrated view of the functional nuclear architecture. Crit Rev Eukaryot Gene Expr 10:179-212.
9. Croft JA, Bridger JM, Boyle S, Perry P, Teague P, Bickmore WA. 1999. Differences in the localization and morphology of chromosomes in the human nucleus. J Cell Biol 14:1119-1131.
10. Fryns JP, Kleczkowska A, Kubien E, Van den Berghe H. 1995. XYY syndrome and other Y chromosome polysomies. Mental status and psychosocial functioning. Genet Couns 6:197-206.
11. Habermann FA, Cremer M, Walter J, Kreth G, von Hase J, Bauer K, Wienberg J, Cremer C, Cremer T, Solovei I. 2001. Arrangements of macro- and microchromosomes in chicken cells. Chromosome Res 9:569-584.
12. Hassold TJ, Jacobs PA. 1984. Trisomy in man. Annu Rev Genet 18:69-97.
13. Iarovaia OV, Bystritskiy A, Ravcheev D, Hancock R, Razin SV. 2004. Visualization of individual DNA loops and a map of loop-domains in the human dystrophin gene. Nucl Acids Res 32:2079-2086.
14. Kim HJ, Kim D, Shin JM, Chung HK, Lee G. 2006. 49, XXXXY syndrome with diabetes mellitus. Horm Res 65:14-17.
15. Kuroda M, Tanabe H, Yoshida K, Oikawa K, Saito A, Kiyuna T, Mizusawa H, Mukai K. 2004. Alteration of chromosome positioning during adipocyte differentiation. J Cell Sci 117:5897-5903.
16. Lukasova E, Kozubek S, Kozubek M, Falk M, Amrichova J. 2002. The 3D structure of human chromosomes in cell nuclei. Chromosome Res 10:535-548.
17. Lyon MF. 1989. X-chromosome inactivation as a system of gene dosage compensation to regulate gene expression. Prog Nucleic Acid Res Mol Biol 36:119-130.
18. Lyon MF. 1999. X-chromosome inactivation. Curr Biol 9:R235-R237.
19. Mayer R, Brero A, von Hase J, Schroeder T, Cremer T, Dietzel S. 2005. Common themes and cell type specific variations of higher order chromatin arrangements in the mouse. BMC Cell Biol 6:44.
20. Murphy WJ, Stanyon R, O'Brien SJ. 2001. Evolution of mammalian genome organization inferred from comparative gene mapping. Genome Biol 2: REVIEWS0005.
21. Murphy WJ, Larkin DM, Everts-van der Wind A, Bourque G, Tesler G, Auvil L, Beever JE, Chowdhary BP, Galibert F, Gatzke L, Hitte C, Meyers SN, Milan D, Ostrander EA, Pape G, Parker HG, Raudsepp T, Rogatcheva MB, Schook LB, Skow LC, Welge M, Womack JE, O'Brien SJ, Pevzner PA, Lewin HA. 2005. Dynamics of mammalian chromosome evolution inferred from multispecies comparative maps. Science 309:613-617.
22. Newberger DS, Blyth SA. 2003. Hypothermia and phenytoin toxicity. Clin Neuropharmacol 26:172-173.
23. Petrova NV, Iarovaia OV, Verbovoy VA, Razin SV. 2005. Specific radial positions of centromeres of human chromosomes X, 1,and 19 remain unchanged in chromatin-depleted nuclei of primary human fibroblasts: Evidence for the organizing role of the nuclear matrix. J Cell Biochem 96:850-857.
24. Rastan S. 1994. X chromosome inactivation and the Xist gene. Curr Opin Genet Dev 4:292-297.
25. Samango-Sprouse C. 2001. Mental development in polysomy X Klinefelter syndrome (47,XXY; 48,XXXY): Effects of incomplete X inactivation. Semin Reprod Med 19:193-202.
26. Stadler S, Schnapp V, Mayer R, Stein S, Cremer C, Bonifer C, Cremer T, Dietzel S. 2004. The architecture of chicken chromosome territories changes during differentiation. BMC Cell Biol 5:44.
27. Swerdlow AJ, Hermon C, Jacobs PA, Alberman E, Beral V, Daker M, Fordyce A, Youings S. 2001. Mortality and cancer incidence in persons with numerical sex chromosome abnormalities: A cohort study. Ann Hum Genet 65:177-188.
28. Taslerova R, Kozubek S, Lukasova E, Jirsova P, Bartova E, Kozubek M. 2003. Arrangement of chromosome 11 and 22 territories, EWSR1 and FLI1 genes, and other genetic elements of these chromosomes in human lymphocytes and Ewing sarcoma cells. Hum Genet 112:143-155.
29. Wattendorf DJ, Muenke M. 2005. Klinefelter syndrome. Am Fam Physician 72:2259-2262.
30. Yurov YB, Soloviev IV, Vorsanova SG, Marcais B, Roizes G, Lewis R. 1996. High resolution multicolor fluorescence in situ hybridization using cyanine and fluorescein dyes: Rapid chromosome identification by directly fluorescently labeled alphoid DNA probes. Hum Genet 97:390-398.
31. Zink D, Amaral MD, Englmann A, Lang S, Clarke LA, Rudolph C, Alt F, Luther K, Braz C, Sadoni N, Rosenecker J, Schindelhauer D. 2004. Transcription-dependent spatial arrangements of CFTR and adjacent genes in human cell nuclei. J Cell Biol 166:815-825.