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Reciprocal translocation and the Philadelphia chromosome.

作者信息

Watt J L, Page B M

出版信息

Hum Genet. 1978 Jun 9;42(2):163-70. doi: 10.1007/BF00283636.

DOI:10.1007/BF00283636
PMID:276514
Abstract

We examined metaphases from three patients with chronic myeloid leukaemia and a typical Philadelphia chromosome with one chromosome 9 as the recipient to determine whether the 9q+22q- translocation is reciprocal. Good quality G-banded photographs of the chromosomes concerned were subjected to light absorption density analysis. This provided enlarged tracings corresponding to the relevant chromosome regions and so facilitated accurate measurement. This technique has unambiguously shown that the typical Philadelphia chromosome results from a reciprocal translocation and that probably no material is gained or lost in the exchange. Furthermorein a total of six patients for whom sequential G and C banding was performed, the chromosome 9 with the largest block of centromeric heterochromatin received the translocated material. We offer tentative explanations for this curious observation.

摘要

相似文献

1
Reciprocal translocation and the Philadelphia chromosome.
Hum Genet. 1978 Jun 9;42(2):163-70. doi: 10.1007/BF00283636.
2
DNA measurements of chromosomes 9 and 22 of six patients with t(9;22) and chronic myeloid leukemia.对6例患有t(9;22)和慢性髓性白血病患者的9号和22号染色体进行DNA测量。
Cytometry. 1980 Sep;1(2):152-5. doi: 10.1002/cyto.990010210.
3
Three chromosomes' (7;9;22) rearrangement and the origin of the Philadelphia chromosome.
Hum Genet. 1978 Aug 31;43(2):133-7. doi: 10.1007/BF00293590.
4
A cellular oncogene is translocated to the Philadelphia chromosome in chronic myelocytic leukaemia.在慢性粒细胞白血病中,一种细胞癌基因易位至费城染色体。
Nature. 1982 Dec 23;300(5894):765-7. doi: 10.1038/300765a0.
5
Role of heterochromatin during preferential 9q;22q translocation in chronic myelogenous leukemia.
Can J Genet Cytol. 1986 Dec;28(6):998-1002. doi: 10.1139/g86-138.
6
Characterization of a complex Philadelphia translocation (1p-;9q+;22q-) by gene mapping.通过基因定位对复杂费城染色体易位(1p-;9q+;22q-)的特征分析
Hum Genet. 1981;58(2):162-5. doi: 10.1007/BF00278702.
7
Unusual translocations involving chromosomes 12;22 and 9;12 in a case of chronic myelogenous leukemia.一例慢性粒细胞白血病患者中涉及12号与22号染色体以及9号与12号染色体的异常易位。
Cancer Genet Cytogenet. 1985 Jan 1;14(1-2):61-5. doi: 10.1016/0165-4608(85)90215-8.
8
"Masked" philadelphia chromosome (Ph1) due to an unusual translocation.因异常易位导致的“隐匿性”费城染色体(Ph1)
Cancer Genet Cytogenet. 1981 Apr;3(3):227-32. doi: 10.1016/0165-4608(81)90088-1.
9
New types of unusual and complex Philadelphia chromosome (Ph1) translocations in chronic myeloid leukemia.
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10
The Philadelphia (Ph) chromosome in leukemia. I. A new mechanism due to interstitial deletion and insertion in chronic myelocytic leukemia.白血病中的费城(Ph)染色体。I. 慢性粒细胞白血病中由于间质缺失和插入导致的一种新机制。
Cancer Genet Cytogenet. 1985 Jan 1;14(1-2):3-10. doi: 10.1016/0165-4608(85)90209-2.

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本文引用的文献

1
Identification of the Philadelphia chromosome as a number 22 by quinacrine mustard fluorescence analysis.
Exp Cell Res. 1970 Nov;63(1):238-40. doi: 10.1016/0014-4827(70)90362-9.
2
Quinacrine mustard fluorescence of human chromosomes: characterization of unusual translocations.人染色体的喹吖因氮芥荧光:异常易位的特征
Am J Hum Genet. 1972 Mar;24(2):189-213.
3
Pachytene analysis in a human reciprocal (10;11) translocation.人类相互易位(10;11)的粗线期分析
J Med Genet. 1973 Sep;10(3):282-7. doi: 10.1136/jmg.10.3.282.
Hum Genet. 1979 Nov 1;52(1):55-67. doi: 10.1007/BF00284598.
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A comment on the paper: reciprocal translocation and the Philadelphia chromosome by Jessie L. Watt and Brenda M. Page, Hum. Genet. 42, 163--170 (1978).对论文《相互易位与费城染色体》的评论,作者杰西·L·瓦特和布伦达·M·佩奇,《人类遗传学》第42卷,第163 - 170页(1978年)
Hum Genet. 1978 Nov 16;44(3):357-8. doi: 10.1007/BF00394302.
4
Identification of chromosome 9 in human male meiosis.人类男性减数分裂中9号染色体的鉴定。
Cytogenet Cell Genet. 1973;12(4):254-63. doi: 10.1159/000130461.
5
The length of the human Y chromosome.人类Y染色体的长度。
Cytogenetics. 1967;6(3):213-27. doi: 10.1159/000129943.
6
Clonal origin of the Philadelphia chromosome from either the paternal or the maternal chromosome number 22.费城染色体的克隆起源于父本或母本的第22号染色体。
Blood. 1974 Jun;43(6):837-40.
7
Letter: A new consistent chromosomal abnormality in chronic myelogenous leukaemia identified by quinacrine fluorescence and Giemsa staining.信件:通过喹吖因荧光和吉姆萨染色鉴定出慢性粒细胞白血病中一种新的一致染色体异常。
Nature. 1973 Jun 1;243(5405):290-3. doi: 10.1038/243290a0.
8
A simple technique for demonstrating centromeric heterochromatin.一种用于显示着丝粒异染色质的简单技术。
Exp Cell Res. 1972 Nov;75(1):304-6. doi: 10.1016/0014-4827(72)90558-7.
9
Human chromosome abnormalities revisited.人类染色体异常再探讨。
Am J Hum Genet. 1972 Mar;24(2):227-8.
10
Attraction between centric heterochromatin of human chromosomes.
Cytogenet Cell Genet. 1975;15(2):66-80. doi: 10.1159/000130503.