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Probable involvement of immunoglobulin superfamily genes in most recurrent chromosomal rearrangements from ataxia telangiectasia.

作者信息

Aurias A, Dutrillaux B

出版信息

Hum Genet. 1986 Mar;72(3):210-4. doi: 10.1007/BF00291879.

DOI:10.1007/BF00291879
PMID:3456975
Abstract

From the chromosomal analysis of 9461 lymphocytes from 57 patients affected by ataxia telangiectasia, it is concluded that bands 7p14, 7q35, 14q12, and 14qter, which are frequently recombined in rearrangements are also too frequently involved in rearrangements with a few other chromosome sites. Among these sites, the most frequently involved are bands 2p11, 2p12, 22q12, and 22q13.2, or the proximal parts of adjacent R-bands. The same rearrangements were observed in a large series of control lymphocytes but their frequencies were much lower than in ataxia telangiectasia. All these recurrent sites of rearrangements, except 22q13.2, are known to be near or at immunoglobulin genes or partially homologous genes like T-cell receptor genes and antigen Leu-2/T8. It is supposed that the rearrangements observed correspond to the visualization at the chromosomal level of illegitimate rearrangements between these genes, and by analogy, that another similar structure may exist on band 22q13.2.

摘要

相似文献

1
Probable involvement of immunoglobulin superfamily genes in most recurrent chromosomal rearrangements from ataxia telangiectasia.
Hum Genet. 1986 Mar;72(3):210-4. doi: 10.1007/BF00291879.
2
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Kroc Found Ser. 1985;19:197-203.
3
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Hum Genet. 1988 Jan;78(1):33-6. doi: 10.1007/BF00291230.
4
Evolution of chromosomal abnormalities in sequential cytogenetic studies of ataxia telangiectasia.共济失调毛细血管扩张症连续细胞遗传学研究中染色体异常的演变
Hum Genet. 1980;55(1):23-9. doi: 10.1007/BF00329122.
5
The chromosome breakpoint at 14q32 in an ataxia telangiectasia t(14;14) T cell clone is different from the 14q32 breakpoint in Burkitts and an inv(14) T cell lymphoma.共济失调毛细血管扩张症t(14;14) T细胞克隆中14q32处的染色体断点与伯基特淋巴瘤及inv(14) T细胞淋巴瘤中14q32处的断点不同。
Hum Genet. 1986 Jul;73(3):254-9. doi: 10.1007/BF00401239.
6
High frequencies of inversions and translocations of chromosomes 7 and 14 in ataxia telangiectasia.共济失调毛细血管扩张症中7号和14号染色体的倒位和易位频率较高。
Mutat Res. 1980 Feb;69(2):369-74. doi: 10.1016/0027-5107(80)90101-3.
7
Growth of large chromosomally abnormal T cell clones in ataxia telangiectasia patients is associated with translocation at 14q11. A model for other T cell neoplasia.共济失调毛细血管扩张症患者中大型染色体异常T细胞克隆的生长与14q11处的易位有关。这是其他T细胞肿瘤形成的一种模式。
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8
New data on clonal anomalies of chromosome 14 in ataxia telangiectasia: tct(14;14) and inv(14).共济失调毛细血管扩张症中14号染色体克隆性异常的新数据:tct(14;14)和inv(14)
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9
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10
Cytogenetic investigations in a family with ataxia telangiectasia.
Hum Genet. 1989 Aug;83(1):79-82. doi: 10.1007/BF00274154.

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3
Growth of large chromosomally abnormal T cell clones in ataxia telangiectasia patients is associated with translocation at 14q11. A model for other T cell neoplasia.

本文引用的文献

1
High frequencies of inversions and translocations of chromosomes 7 and 14 in ataxia telangiectasia.共济失调毛细血管扩张症中7号和14号染色体的倒位和易位频率较高。
Mutat Res. 1980 Feb;69(2):369-74. doi: 10.1016/0027-5107(80)90101-3.
2
Localization of human immunoglobulin kappa light chain variable region genes to the short arm of chromosome 2 by in situ hybridization.通过原位杂交将人免疫球蛋白κ轻链可变区基因定位于2号染色体短臂。
Proc Natl Acad Sci U S A. 1982 Aug;79(16):4957-61. doi: 10.1073/pnas.79.16.4957.
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Human immunoglobulin heavy chain genes map to a region of translocations in malignant B lymphocytes.
共济失调毛细血管扩张症患者中大型染色体异常T细胞克隆的生长与14q11处的易位有关。这是其他T细胞肿瘤形成的一种模式。
Hum Genet. 1987 Aug;76(4):389-95. doi: 10.1007/BF00272451.
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Molecular characterization of different ataxia telangiectasia T-cell clones. I. A common breakpoint at the 14q11.2 band splits the T-cell receptor alpha-chain gene.
Hum Genet. 1988 Jan;78(1):33-6. doi: 10.1007/BF00291230.
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Juxtaposition of the T-cell receptor alpha-chain locus (14q11) and a region (14q32) of potential importance in leukemogenesis by a 14;14 translocation in a patient with T-cell chronic lymphocytic leukemia and ataxia-telangiectasia.一名患有T细胞慢性淋巴细胞白血病和共济失调毛细血管扩张症的患者,因14号与14号染色体易位,导致T细胞受体α链基因座(14q11)与白血病发生中可能具有重要意义的一个区域(14q32)并置。
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Hum Genet. 1988 Aug;79(4):360-4. doi: 10.1007/BF00282177.
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Hum Genet. 1989 Sep;83(2):133-8. doi: 10.1007/BF00286705.
9
Analysis of 7 polymorphic markers at chromosome 11q22-23 in 35 ataxia telangiectasia families; further evidence of linkage.对35个共济失调毛细血管扩张症家系中11号染色体q22 - 23区域的7个多态性标记进行分析;连锁的进一步证据。
Hum Genet. 1990 Jul;85(2):215-20. doi: 10.1007/BF00193199.
10
The chromosome translocation (11;14)(p13;q11) associated with T cell acute leukemia. Asymmetric diversification of the translocational junctions.与T细胞急性白血病相关的染色体易位(11;14)(p13;q11)。易位连接点的不对称多样化。
J Exp Med. 1990 Feb 1;171(2):489-501. doi: 10.1084/jem.171.2.489.
人类免疫球蛋白重链基因定位于恶性B淋巴细胞的易位区域。
Science. 1982 Apr 16;216(4543):301-3. doi: 10.1126/science.6801764.
4
Inversion (14)(q12qter) or (q11.2q32.3): the most frequently acquired rearrangement in lymphocytes.倒位(14)(q12q末端)或(q11.2q32.3):淋巴细胞中最常见的获得性重排。
Hum Genet. 1985;71(1):19-21. doi: 10.1007/BF00295660.
5
Chromosomal localization of the human T cell receptor beta-chain genes.人类T细胞受体β链基因的染色体定位
Cell. 1985 May;41(1):335. doi: 10.1016/0092-8674(85)90086-8.
6
Genes for beta chain of human T-cell antigen receptor map to regions of chromosomal rearrangement in T cells.人类T细胞抗原受体β链的基因定位于T细胞染色体重排区域。
Science. 1985 May 3;228(4699):582-5. doi: 10.1126/science.3983642.
7
Location of gene for beta subunit of human T-cell receptor at band 7q35, a region prone to rearrangements in T cells.人类T细胞受体β亚基基因位于7q35带,该区域在T细胞中易于发生重排。
Science. 1985 May 3;228(4699):580-2. doi: 10.1126/science.3983641.
8
Gene for alpha-chain of human T-cell receptor: location on chromosome 14 region involved in T-cell neoplasms.人类T细胞受体α链基因:位于14号染色体上与T细胞肿瘤相关的区域。
Science. 1985 Mar 1;227(4690):1044-7. doi: 10.1126/science.3919442.
9
Gene for the human T cell differentiation antigen Leu-2/T8 is closely linked to the kappa light chain locus on chromosome 2.人类T细胞分化抗原Leu-2/T8的基因与2号染色体上的κ轻链基因座紧密连锁。
J Exp Med. 1985 Feb 1;161(2):429-34. doi: 10.1084/jem.161.2.429.
10
Human gamma-chain genes are rearranged in leukaemic T cells and map to the short arm of chromosome 7.人类γ链基因在白血病T细胞中发生重排,并定位于7号染色体短臂。
Nature. 1985;316(6028):549-52. doi: 10.1038/316549a0.