Petit M M, Mols R, Schoenmakers E F, Mandahl N, Van de Ven W J
Laboratory for Molecular Oncology, Center for Human Genetics, University of Leuven and Flanders Interuniversity Institute for Biotechnology, Herestraat 49, Leuven, B-3000, Belgium.
Genomics. 1996 Aug 15;36(1):118-29. doi: 10.1006/geno.1996.0432.
A major cytogenetic subgroup of lipomas is characterized by recurrent chromosome aberrations, mainly translocations, that involve chromosome segment 12q13-q15. Multiple chromosomes have been found as the translocation partners of chromosome 12 but 3q27-q28 is preferentially involved. In previous studies, it has been shown that the high mobility group (HMG) protein gene HMGIC at 12q15 is consistently rearranged as a consequence of these translocations. Here, we report the identification and characterization of the chromosome 3-derived translocation partner gene, which we have designated LPP (lipoma preferred partner gene). Using 3'-RACE analysis of HMGIC fusion transcripts in lipoma cell line Li-501/SV40, ectopic genetic sequences were obtained, which by CASH (chromosome assignment using somatic cell hybrids) and FISH (fluorescence in situ hybridization) analysis were found to originate from chromosome segment 3q27-q28. In Northern blot analysis, an mRNA of over 10 kb was detected by these ectopic sequences in a variety of human tissues but not in brain and peripheral blood leukocytes. Upon partial cDNA cloning, features of the genetic organization of LPP were established. The gene was found to span a genomic region of over 400 kb. Nucleotide sequence analysis of a composite cDNA of LPP revealed an open reading frame of 1836 nucleotides encoding a proline-rich protein containing a leucine-zipper motif in its amino-terminal region and three LIM domains in its carboxy-terminal region. The LPP-encoded protein should be classified as a novel member of the group 3 proteins of the LIM protein gene family. Using reverse transcriptase combined with polymerase chain reactions in the analysis of a number of lipoma cell lines and primary lipomas, it appeared that LPP is frequently rearranged also in cases without a cytogenetically detectable involvement of 3q27-q28. Two alternative HMGIC/LPP hybrid transcripts have been detected; the difference between them is mainly the presence of either two or three LIM domains in the predicted HMGI-C/LPP fusion proteins.
脂肪瘤的一个主要细胞遗传学亚组的特征是存在反复出现的染色体畸变,主要是易位,涉及染色体12q13 - q15区段。已发现多条染色体是12号染色体的易位伙伴,但3q27 - q28区段优先受累。在以往的研究中,已表明位于12q15的高迁移率族(HMG)蛋白基因HMGIC因这些易位而持续发生重排。在此,我们报告了3号染色体衍生的易位伙伴基因的鉴定和特征,我们将其命名为LPP(脂肪瘤优先伙伴基因)。利用脂肪瘤细胞系Li - 501/SV40中HMGIC融合转录本的3'-RACE分析,获得了异位遗传序列,通过体细胞杂交染色体定位(CASH)和荧光原位杂交(FISH)分析发现这些序列源自3q27 - q28染色体区段。在Northern印迹分析中,这些异位序列在多种人体组织中检测到一条超过10 kb的mRNA,但在脑和外周血白细胞中未检测到。通过部分cDNA克隆,确定了LPP的基因组织结构特征。发现该基因跨越超过400 kb的基因组区域。LPP复合cDNA的核苷酸序列分析揭示了一个1836个核苷酸的开放阅读框,编码一种富含脯氨酸的蛋白,该蛋白在其氨基末端区域含有一个亮氨酸拉链基序,在其羧基末端区域含有三个LIM结构域。LPP编码的蛋白应归类为LIM蛋白基因家族3类蛋白的一个新成员。在对多个脂肪瘤细胞系和原发性脂肪瘤的分析中,使用逆转录酶结合聚合酶链反应,发现在一些细胞遗传学上未检测到3q27 - q28受累的病例中,LPP也经常发生重排。已检测到两种不同的HMGIC/LPP杂交转录本;它们之间的差异主要在于预测的HMGI - C/LPP融合蛋白中存在两个或三个LIM结构域。