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尽管克氏锥虫的染色体大小存在广泛差异,但染色体特异性标记揭示了保守的连锁群。

Chromosome specific markers reveal conserved linkage groups in spite of extensive chromosomal size variation in Trypanosoma cruzi.

作者信息

Henriksson J, Porcel B, Rydåker M, Ruiz A, Sabaj V, Galanti N, Cazzulo J J, Frasch A C, Pettersson U

机构信息

Department of Medical Genetics, University of Uppsala, Sweden.

出版信息

Mol Biochem Parasitol. 1995 Jul;73(1-2):63-74. doi: 10.1016/0166-6851(95)00096-j.

Abstract

The karyotypes of three cloned stocks, CL Brener (CL), CA I/72 (CA) and Sylvio X10/7 (X10), of Trypanosoma cruzi were studied by pulsed-field gel electrophoresis followed by ethidium bromide staining and hybridization with 35 different probes, 30 of which identified single chromosomes. The chromosome-specific probes identified between 26 and 31 chromosomal bands in the three cloned stocks, corresponding to 20 unique chromosomes in CL and 19 in CA and X10. Considering the DNA content of the parasite, it was predicted that the markers recognise at least half of all T. cruzi chromosomes. A majority of identified chromosomes showed large differences in size among different strains, in some cases by up to 50%. Interestingly, CL had in general larger chromosomes than the two other studied cloned stocks. Several of the markers showed linkage and nine different linkage groups were identified, each comprising 2-4 markers. The linkage between the markers was maintained in 8 of the 9 linkage groups when a panel comprising 26 different T. cruzi strains representing major T. cruzi populations was tested. One linkage group was found to be maintained in some strains but not in others. This result shows that chromosomal rearrangements occur in the T. cruzi genome, albeit with a low frequency. Repetitive DNA, both non-coding and in one case coding, was more abundant in the cloned stock CL Brener than in CA and X10. The information presented will make it possible to select chromosomes for the construction of physical chromosomal maps required for the T. cruzi genome project.

摘要

通过脉冲场凝胶电泳,随后进行溴化乙锭染色以及与35种不同探针杂交,对克氏锥虫的三个克隆株系CL Brener(CL)、CA I/72(CA)和Sylvio X10/7(X10)的核型进行了研究。其中30种探针可识别单条染色体。这些染色体特异性探针在三个克隆株系中识别出26至31条染色体带,对应于CL中的20条独特染色体以及CA和X10中的19条。考虑到寄生虫的DNA含量,预计这些标记识别出了至少一半的克氏锥虫染色体。大多数已识别的染色体在不同菌株间显示出大小上的巨大差异,某些情况下差异高达50%。有趣的是,总体而言CL的染色体比其他两个研究的克隆株系更大。一些标记显示出连锁关系,共识别出九个不同的连锁群,每个连锁群包含2 - 4个标记。当对一个包含代表克氏锥虫主要群体的26种不同克氏锥虫菌株的样本进行测试时,9个连锁群中有8个的标记间连锁关系得以维持。发现一个连锁群在某些菌株中得以维持,而在其他菌株中则不然。这一结果表明克氏锥虫基因组中发生了染色体重排,尽管频率较低。在克隆株系CL Brener中,非编码和一种情况下的编码重复DNA比CA和X10中更为丰富。所呈现的信息将使得为克氏锥虫基因组计划构建所需的物理染色体图谱选择染色体成为可能。

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