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通过原位杂交将人类聚集蛋白聚糖基因AGC1定位于15q25→q26.2。

Assignment of the human aggrecan gene AGC1 to 15q25-->q26.2 by in situ hybridization.

作者信息

Just W, Klett C, Vetter U, Vogel W

机构信息

Abteilung Klinische Genetik, Universität Ulm, Germany.

出版信息

Hum Genet. 1993 Nov;92(5):516-8. doi: 10.1007/BF00216462.

DOI:10.1007/BF00216462
PMID:8244345
Abstract

The human aggrecan gene (AGC1) has been localized to 15q25-->q26.2 by in situ hybridization. Although no genetic diseases of connective tissue map to this location, the malignant melanoma-associated surface antigen mel-CSPG is located here; mel-CSPG is a chondroitin sulfate proteoglycan. This raises the possibility that AGC1 and mel-CSPG may be the same gene.

摘要

通过原位杂交技术,已将人类聚集蛋白聚糖基因(AGC1)定位于15q25→q26.2。尽管尚无结缔组织遗传病定位于此区域,但恶性黑色素瘤相关表面抗原mel-CSPG位于此处;mel-CSPG是一种硫酸软骨素蛋白聚糖。这就增加了AGC1和mel-CSPG可能是同一基因的可能性。

相似文献

1
Assignment of the human aggrecan gene AGC1 to 15q25-->q26.2 by in situ hybridization.通过原位杂交将人类聚集蛋白聚糖基因AGC1定位于15q25→q26.2。
Hum Genet. 1993 Nov;92(5):516-8. doi: 10.1007/BF00216462.
2
Assignment of the human aggrecan gene (AGC1) to 15q26 using fluorescence in situ hybridization analysis.运用荧光原位杂交分析将人类聚集蛋白聚糖基因(AGC1)定位于15q26。
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Human melanoma proteoglycan: expression in hybrids controlled by intrinsic and extrinsic signals.人黑色素瘤蛋白聚糖:在由内在和外在信号控制的杂交体中的表达。
Science. 1986 Mar 14;231(4743):1281-4. doi: 10.1126/science.3633135.
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Am J Pathol. 1989 Feb;134(2):295-303.
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2
Localisation of a gene for an autosomal recessive syndrome of macrocephaly, multiple epiphyseal dysplasia, and distinctive facies to chromosome 15q26.一种常染色体隐性遗传的巨头畸形、多发性骨骺发育异常及特殊面容综合征的致病基因定位于15号染色体长臂26区。
J Med Genet. 2001 Jun;38(6):369-73. doi: 10.1136/jmg.38.6.369.
3
Molecular cloning of a human melanoma-associated chondroitin sulfate proteoglycan.

本文引用的文献

1
Human decorin gene: intron-exon junctions and chromosomal localization.人类核心蛋白聚糖基因:内含子-外显子连接及染色体定位
Genomics. 1993 Jan;15(1):161-8. doi: 10.1006/geno.1993.1023.
2
The morbid anatomy of the human genome: chromosomal location of mutations causing disease.人类基因组的病理解剖学:导致疾病的突变的染色体定位。
J Med Genet. 1993 Jan;30(1):1-26. doi: 10.1136/jmg.30.1.1.
3
Absence of proteoglycan core protein in cartilage from the cmd/cmd (cartilage matrix deficiency) mouse.cmd/cmd(软骨基质缺乏)小鼠软骨中蛋白聚糖核心蛋白缺失。
一种人类黑色素瘤相关硫酸软骨素蛋白聚糖的分子克隆
Proc Natl Acad Sci U S A. 1996 Sep 3;93(18):9710-5. doi: 10.1073/pnas.93.18.9710.
4
Structure of the human aggrecan gene: exon-intron organization and association with the protein domains.人类聚集蛋白聚糖基因的结构:外显子-内含子组织及其与蛋白质结构域的关联。
Biochem J. 1995 Jul 15;309 ( Pt 2)(Pt 2):535-42. doi: 10.1042/bj3090535.
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Human melanoma proteoglycan: expression in hybrids controlled by intrinsic and extrinsic signals.人黑色素瘤蛋白聚糖:在由内在和外在信号控制的杂交体中的表达。
Science. 1986 Mar 14;231(4743):1281-4. doi: 10.1126/science.3633135.
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Mapping of the oncogenes Myc, Sis, and int-1 to the distal part of mouse chromosome 15.
Cytogenet Cell Genet. 1987;44(2-3):65-8. doi: 10.1159/000132345.
6
Complete coding sequence and deduced primary structure of the human cartilage large aggregating proteoglycan, aggrecan. Human-specific repeats, and additional alternatively spliced forms.人软骨大聚合蛋白聚糖(聚集蛋白聚糖)的完整编码序列及推导的一级结构。人特异性重复序列及其他可变剪接形式。
J Biol Chem. 1991 Jan 15;266(2):894-902.
7
Human biglycan gene. Putative promoter, intron-exon junctions, and chromosomal localization.人类双糖链蛋白聚糖基因。推定启动子、内含子-外显子连接区及染色体定位。
J Biol Chem. 1991 Aug 5;266(22):14371-7.
8
Elevated sister chromatid exchange phenotype of Bloom syndrome cells is complemented by human chromosome 15.人类15号染色体可互补布鲁姆综合征细胞中升高的姐妹染色单体交换表型。
Proc Natl Acad Sci U S A. 1992 Sep 1;89(17):7968-72. doi: 10.1073/pnas.89.17.7968.
9
Mapping of the versican proteoglycan gene (CSPG2) to the long arm of human chromosome 5 (5q12-5q14).
Genomics. 1992 Dec;14(4):845-51. doi: 10.1016/s0888-7543(05)80103-x.
10
The induction of arthritis in mice by the cartilage proteoglycan aggrecan: roles of CD4+ and CD8+ T cells.
Cell Immunol. 1992 Oct 15;144(2):347-57. doi: 10.1016/0008-8749(92)90250-s.