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脂肪瘤、多形性腺瘤、子宫平滑肌瘤和黏液样脂肪肉瘤中12号染色体q臂断点的物理图谱。

Physical mapping of chromosome 12q breakpoints in lipoma, pleomorphic salivary gland adenoma, uterine leiomyoma, and myxoid liposarcoma.

作者信息

Schoenmakers E F, Kools P F, Mols R, Kazmierczak B, Bartnitzke S, Bullerdiek J, Dal Cin P, De Jong P J, Van den Berghe H, Van de Ven W J

机构信息

Center for Human Genetics, University of Leuven, Belgium.

出版信息

Genomics. 1994 Mar 15;20(2):210-22. doi: 10.1006/geno.1994.1155.

Abstract

We report here the physical mapping of recurrent chromosome 12q13-q15 breakpoints in cell lines derived from primary myxoid liposarcoma, lipoma, uterine leiomyoma, and pleomorphic adenoma of the salivary glands. In fluorescence in situ hybridization (FISH) experiments, we first mapped the position of the chromosome 12 translocation breakpoint in uterine leiomyoma cell line LM-30.1/SV40 relative to loci COL2A1, D12S4, D12S17, D12S6, D12S6, D12S19, D12S8, and D12S7. It mapped between linkage probes CRI-C86 (D12S19) and p7G11 (D12S8). We then isolated YAC clones using CRI-C86- and p7G11-derived sequence-tagged sites, constructed corresponding YAC contigs of 310 and 800 kb, respectively, and established long-range physical maps of these. Cosmid clones LLNL12NCO1-98C10 and LLNL12NCO1-113D12 were isolated using STSs within the CRI-C86- and the p7G11-derived YAC contigs, respectively, and a mixture of them was used to routinely study the various tumor cell lines by FISH analysis. The chromosome 12 breakpoints of all tumor cell lines tested mapped between cosmids LLNL12NCO1-98C10 and LLNL12NCO1-113D12. None of the breakpoints appeared to map within any of the isolated YAC clones. Furthermore, FISH analysis using cosmid LLNL12-NCO1-144G3, which maps at the CHOP locus, revealed that the chromosome 12 breakpoints in all cell lines of the three benign solid tumors that were tested were located distal to the chromosome 12 translocation breakpoint with the CHOP gene in myxoid liposarcoma cells with t(12;16). In conclusion, our studies seem to indicate that the chromosome 12 breakpoints of myxoid liposarcoma, lipoma, uterine leiomyoma, and pleomorphic adenoma of the salivary glands are all clustered within the 7-cM interval between D12S19 and D12S8, with those of the benign solid tumors distal to CHOP. Finally, the MYF5 gene mapped telomeric to LLNL12NCO1-113D12, and the MIP gene mapped centromeric to the chromosome 12 translocation breakpoint in myxoid liposarcoma cells.

摘要

我们在此报告了来自原发性黏液样脂肪肉瘤、脂肪瘤、子宫平滑肌瘤和涎腺多形性腺瘤的细胞系中12号染色体q13 - q15区域反复出现的染色体断点的物理图谱。在荧光原位杂交(FISH)实验中,我们首先将子宫平滑肌瘤细胞系LM - 30.1/SV40中12号染色体易位断点的位置相对于COL2A1、D12S4、D12S17、D12S6、D12S6、D12S19、D12S8和D12S7等基因座进行定位。它定位于连锁探针CRI - C86(D12S19)和p7G11(D12S8)之间。然后,我们使用源自CRI - C86和p7G11的序列标签位点分离酵母人工染色体(YAC)克隆,分别构建了310 kb和800 kb的相应YAC重叠群,并建立了它们的长距离物理图谱。分别使用源自CRI - C86和p7G11的YAC重叠群中的序列标签位点(STS)分离出黏粒克隆LLNL12NCO1 - 98C10和LLNL12NCO1 - 113D12,并将它们的混合物用于通过FISH分析常规研究各种肿瘤细胞系。所有测试的肿瘤细胞系的12号染色体断点都定位于黏粒LLNL12NCO1 - 98C10和LLNL12NCO1 - 113D12之间。似乎没有任何断点定位于任何分离出的YAC克隆内。此外,使用定位于CHOP基因座的黏粒LLNL12 - NCO1 - 144G3进行FISH分析显示,在检测的三种良性实体瘤的所有细胞系中,12号染色体断点位于具有t(12;16)的黏液样脂肪肉瘤细胞中与CHOP基因发生12号染色体易位断点的远端。总之,我们的研究似乎表明,黏液样脂肪肉瘤、脂肪瘤、子宫平滑肌瘤和涎腺多形性腺瘤的12号染色体断点都聚集在D12S19和D12S8之间7厘摩的区间内,良性实体瘤的断点位于CHOP远端。最后,MYF5基因定位于LLNL12NCO1 - 113D12的端粒侧,而MIP基因定位于黏液样脂肪肉瘤细胞中12号染色体易位断点的着丝粒侧。

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