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慢性髓性白血病中人类免疫球蛋白λ轻链在费城染色体上的区域定位。

Regional mapping of the human immunoglobulin lambda light chain to the Philadelphia chromosome in chronic myeloid leukaemia.

作者信息

Goyns M H, Young B D, van Kessel A G, de Klein A, Grosveld G, Bartram C R, Bootsma D

出版信息

Leuk Res. 1984;8(4):547-53. doi: 10.1016/0145-2126(84)90003-1.

DOI:10.1016/0145-2126(84)90003-1
PMID:6433113
Abstract

The lambda light chain immunoglobulin constant region (C lambda) locus was mapped on human chromosome 22. A DNA probe containing part of the C lambda locus was isolated from a human chromosome 22 genomic library, and a series of rodent X human somatic cell hybrids (each of which contained different translocated parts of chromosome 22) were constructed and characterized. The hybridization of the C lambda probe to DNA from these cell hybrids was then studied by Southern blot analysis. The results demonstrates that the C lambda locus is situated very close to the translocation breakpoint on human chromosome 22 which is characteristic of chronic myeloid leukaemia, and at least part if not at all of the locus is situated on the Philadelphia chromosome.

摘要

λ轻链免疫球蛋白恒定区(Cλ)基因座被定位在人类22号染色体上。从人类22号染色体基因组文库中分离出一个包含部分Cλ基因座的DNA探针,并构建和鉴定了一系列啮齿动物×人类体细胞杂种(每个杂种包含22号染色体的不同易位部分)。然后通过Southern印迹分析研究Cλ探针与这些细胞杂种DNA的杂交情况。结果表明,Cλ基因座非常靠近人类22号染色体上慢性髓性白血病所特有的易位断点,并且该基因座至少部分(如果不是全部)位于费城染色体上。

相似文献

1
Regional mapping of the human immunoglobulin lambda light chain to the Philadelphia chromosome in chronic myeloid leukaemia.慢性髓性白血病中人类免疫球蛋白λ轻链在费城染色体上的区域定位。
Leuk Res. 1984;8(4):547-53. doi: 10.1016/0145-2126(84)90003-1.
2
The breakpoint of the Philadelphia chromosome 22 in chronic myeloid leukaemia is distal to the immunoglobulin lambda light chain constant region genes.慢性髓细胞白血病中费城染色体22的断点位于免疫球蛋白λ轻链恒定区基因的远端。
Mol Biol Med. 1983 Jul;1(1):11-9.
3
Chromosomal orientation of the lambda light chain locus: V lambda is proximal to C lambda in 22q11.λ轻链基因座的染色体定位:Vλ在22q11中靠近Cλ。
Nucleic Acids Res. 1985 Jan 25;13(2):381-7. doi: 10.1093/nar/13.2.381.
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Lambda Ig constant region genes are translocated to chromosome 8 in Burkitt's lymphoma with t(8;22).在伴有t(8;22)的伯基特淋巴瘤中,λ免疫球蛋白恒定区基因易位至8号染色体。
Nucleic Acids Res. 1983 Feb 25;11(4):1133-42. doi: 10.1093/nar/11.4.1133.
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In situ hybridization and translocation breakpoint mapping. II. Two unusual t(21;22) translocations.原位杂交与易位断点图谱分析。II. 两个不寻常的t(21;22)易位
Cytogenet Cell Genet. 1985;39(3):173-8. doi: 10.1159/000132130.
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Mapping of the c-sis oncogene on human chromosome 22 with respect to the breakpoint associated with chronic myeloid leukaemia.
Biosci Rep. 1983 Dec;3(12):1107-11. doi: 10.1007/BF01120203.
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Chromosomal location of human kappa and lambda immunoglobulin light chain constant region genes.人类κ和λ免疫球蛋白轻链恒定区基因的染色体定位。
J Exp Med. 1982 May 1;155(5):1480-90. doi: 10.1084/jem.155.5.1480.
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In situ hybridization and translocation breakpoint mapping. III. DiGeorge syndrome with partial monosomy of chromosome 22.原位杂交与易位断点图谱分析。III. 伴有22号染色体部分单体性的迪格奥尔格综合征
Cytogenet Cell Genet. 1985;39(3):179-83. doi: 10.1159/000132131.
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Regional mapping of two human immunoglobulin V lambda genes and analysis of the V lambda locus in chronic myeloid leukaemia.两个人类免疫球蛋白Vλ基因的区域定位及慢性髓性白血病中Vλ基因座的分析
Nucleic Acids Res. 1985 Aug 26;13(16):5761-70. doi: 10.1093/nar/13.16.5761.
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V lambda and J lambda-C lambda gene segments of the human immunoglobulin lambda light chain locus are separated by 14 kb and rearrange by a deletion mechanism.人类免疫球蛋白λ轻链基因座的Vλ和Jλ-Cλ基因片段相隔14 kb,并通过缺失机制进行重排。
Eur J Immunol. 1991 Jun;21(6):1513-22. doi: 10.1002/eji.1830210627.

引用本文的文献

1
Physical location of the human immunoglobulin lambda-like genes, 14.1, 16.1, and 16.2.人类免疫球蛋白λ样基因的物理位置,14.1、16.1和16.2。
Immunogenetics. 1993;38(6):387-99. doi: 10.1007/BF00184519.
2
Cloning and sequence analysis of an Ig lambda light chain mRNA expressed in the Burkitt's lymphoma cell line EB4.在伯基特淋巴瘤细胞系EB4中表达的Igλ轻链mRNA的克隆与序列分析。
Nucleic Acids Res. 1985 Apr 25;13(8):2931-41. doi: 10.1093/nar/13.8.2931.
3
Regional mapping of two human immunoglobulin V lambda genes and analysis of the V lambda locus in chronic myeloid leukaemia.
两个人类免疫球蛋白Vλ基因的区域定位及慢性髓性白血病中Vλ基因座的分析
Nucleic Acids Res. 1985 Aug 26;13(16):5761-70. doi: 10.1093/nar/13.16.5761.
4
A new polymorphic probe on chromosome 22: NB5 (D22S201).22号染色体上一种新的多态性探针:NB5(D22S201)。
Nucleic Acids Res. 1991 Apr 25;19(8):1963. doi: 10.1093/nar/19.8.1963.
5
A new polymorphic probe on chromosome 22q: NB129 (D22S193).22号染色体上的一种新的多态性探针:NB129(D22S193)。
Nucleic Acids Res. 1991 Feb 11;19(3):687.
6
A new polymorphic probe on chromosome 22: NB84 (D22S183).22号染色体上的一种新的多态性探针:NB84(D22S183)。
Nucleic Acids Res. 1991 Feb 11;19(3):687.
7
A new polymorphic probe on chromosome 22: NB35 (D22S182).位于22号染色体上的一种新型多态性探针:NB35(D22S182)。
Nucleic Acids Res. 1991 Feb 11;19(3):686.
8
A new polymorphic probe on chromosome 22: NB17 (D22S181).22号染色体上一种新的多态性探针:NB17(D22S181)。
Nucleic Acids Res. 1991 Feb 11;19(3):686.