Study of hematopoietic clopolity using X-chromosome inactivation mosaicism and its application to essential thrombocythemia;Étude de la clonalité dans la thrombocytémie essentielle

Hematologie

Volumn 2, Issue 6, 1996, Pages 531-536

  El Kassar, Nahed ^a  

^a INSERM   (France)

Author keywords

Clonality; Essential thrombocythemia; Hematopoiesis; Skewed inactivation pattern; X chromosome

Indexed keywords

CHROMOSOME MOSAICISM; HEMATOPOIESIS; HUMAN; REVIEW; THROMBOCYTHEMIA; X CHROMOSOME;

EID: 0030512247     PISSN: 12647527     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Review

References (28)

1. Murphy S, Iland H, Rosenthal D, Laszlo J. Essential thrombocythemia: an interim report from the Patycythemia Vera Study Group. Blood 1986 ; 23 : 177-82.
2. Vogelstein B, Fearon ER, Hamilton SR, Feinberg AP. Use of restriction fragment length polymorphisms to determine the clonal origin of human tumors. Science 1985 ; 227 : 642-5.
3. Simmler MC. L'inactivarion du chromosome X chez les mammifères. médecine/sciences 1992 ; 8 : 972-8.
4. Lyon MF. Gene action in the X chromosome of the mouse. Nature 1961 ; 190 : 372-3.
5. Allen RC, Zoghbi HY, Moseley AB, Rosenblatt HM, Belmont JW. Methylation of Hpall and Hhal sites near the polymorphic CAG repeat in the human androgen-receptor gene correlates with X chromosome inactivation. Am J Hum Genet 1992 ; 51 : 1229-39.
6. Ellis N, Goodfellow PN. The mammalian pseudoautosomal region. Trends Genet 1989 ; 5 : 406-10.
7. Cattanach BM. Control of chromosome inactivation. Ann Rev Genet 1975 ; 75 : 1-18.
8. Tan SS, Williams EA, Tam PPL. X-chromosome inactivation occurs at different times in different tissues of the post-implantation mouse embryon. Nat Genet 1993 ; 3 : 170-4.
9. Brockdorff N, Ashworth A, Graham FK, McCobe VM, Norris DP, Cooper PJ, Swift S, Rastan S. The product of mouse Xist gene is a 15kb inactive X-specific transcript containing no conservative ORF and located in the nucleus. Cell 1992 ; 71 : 515-26.
10. Rastan S, Cattanach BM. Interaction between the Xce and imprinting of the paternel X chromosome in mouse yolk-sac endoderm. Nature 1983 ; 303 : 635-7.
11. Young NS. The problem of clonality in aplastic anemia : Dr Dameshek's riddle, restated. Blood 1992 ; 79 : 1385-92.
12. Gale R, Wheadon H, Boulos P, Linch DC. Tissue specificity of X chromosome inactivation patterns Blood 1994; 83: 2899-905.
13. Prchal JT, Guan YL. A novel donality assay based on transcriptional analysis of The active X-chromosome. Stem Cells 1993 ; 11 (suppl. 1) : 62-5.
14. Babinet C, Barra J, Renard JP. Le marquage et l'expression différentiels des genomes paternel et maternel. médecine/sciences 1989; 5 : 972-8.
15. Fey MF, Liechti-Gallati S, Rohr A von, Borisch B, Theilkäs L, Schneider V, Oestreic̈hër M, Nagel S, Ziemiecki A, Tabler A. Clonality and X-inactivafron patterns in hematopoietic cell populations detected by highly informative M27b DMA probe. Blood 1994 ; 83 : 931-8.
16. Busque L, Mio R, Mattioli J, Brais E, Blais N, Lalonde Y, Maragh M, Gilliland DG. Nonrandom X-inacrivation patterns in normal Females: lyonization ratios vary with age. Blood 1996 ; 88 : 59-65.
17. El-Kassar N, Hetet G, Brière J, Grand-champ B. Etude de l'inactivation du chromosome X chez les témoins sains: comparaison des techniques avec l'âge. [Abstract 37] Hematology and Cell Therapy 1996 ; 38.
18. Fialkow PJ, Faguet GB, Jacobson RJ, Vaidya K, Murphy S. Evidence that essential thrombocythemia is a clonal disorder with origin in a multipotent stem cell. Blood 1981 ; 58 : 916-9.
19. Medneraneon subject. Blood 1982 ; 59 : 70-9.
20. Lucas GS, Padua RA, Masters GS, Oscier DG, Jacobs A. The application of X chromosome gene probes to the diagnosis of myeloprolifsrotive disease. Br J Haematol 1989 ; 72 : 530-3.
21. Anger B, Janssen JWG, Schrezenmeier H, Hehlmann R, Heimpel H, Bartram CR. Clonal analysis of chronic myeloproliferative disorders using X-linked DNA polymorphisms. Leukemia 1990, 4 : 258-61.
22. Janssen JWG, Anger BR, Drexler HG, Bartram CR, Heimpel H. Essential thrombocythemia in two sisters originating from different stem cell levels. Blood 1990 ; 75 : 1633-6.
23. Turhan AG, Coshman JD, Eaves CJ, Humphries RK, Eaves AC. Variable expression of features of normal and neoplastic stem cells in patients with thrombocytosis. Br J Haematol 1992 ; 82 : 50-7.
24. Tsukamoto N, Morita K, Maehara T, Okamoto K, Sakai H. Clonality in chnonic myeloproliferative disorders defined by X-chromosome linked probes : demonstration of heterogeneity in lineage involvement. Br J Haematol 1994 ; 86 : 253-8.
25. EhKassar N, Hetet G, Brière J, Grand-champ B. Clonal analysis of haematopoietic cells in essential thrombocythaemia. Br J Haematol 1995 ; 90 : 131-7.
26. Jinnai I, Yoshida S, Toyoda A, Murohashi I, Bessho M, Hiroshima K, Nagai K, Tomonaga M, Boyd Y. A clonal study of hemalopoiesis using the M27 β probe : abberant band patterns caused by incomplete digestion of a methyl-sensitive enzyme in the inactive X-chromosome. Leukemia 1993 ; 7 : 1432-6.
27. Prchal JT, Liu Y, Prchal JF, Hoffman R, Tushinski R Are normal stem cells present in myeloproliferative syndrome? [Abstract 207]. Blood 1994 ; 84 (suppl. 1).
28. El-Kassar N, Hetet G, Brière J, Grand-champ B. Cionality analysis in essential thrombocythemia : advantages of studying platelets and T lymphocytes. [Abstract 182]. Blood 1995 ; 86 (suppl. 1).