Kimura Shuichi, Omasa Takeshi
Graduate School of Advanced Technology and Science, Tokushima University, Tokushima, 770-8506, Japan.
Faculty of Bioscience and Bioindustry, Tokushima University, Tokushima, 770-8506, Japan.
Cytotechnology. 2018 Oct;70(5):1399-1407. doi: 10.1007/s10616-018-0233-5. Epub 2018 Jul 9.
Chinese hamster ovary (CHO) cells have frequently been used in biotechnology as a mammalian host cell platform for expressing genes of interest. Previously, we constructed a detailed physical chromosomal map of the CHO DG44 cell line by fluorescence in situ hybridization (FISH) imaging using 303 bacterial artificial chromosome (BAC) clones as hybridization probes (BAC-FISH). BAC-FISH results revealed that the two longest chromosomes were completely paired. However, other chromosomes featured partial deletions or rearrangements. In this study, we determined the end sequences of 303 BAC clones (BAC end sequences), which were used for BAC-FISH probes. Among 606 BAC-end sequences (BESs) (forward and reverse ends), 558 could be determined. We performed a comparison between all determined BESs and mouse genome sequences using NCBI BLAST. Among these 558 BESs, 465 showed high homology to mouse chromosomal sequences. We analyzed the locations of these BACs in chromosomes of the CHO DG44 cell line using a physical chromosomal map. From the obtained results, we investigated the regional similarities among CHO chromosomes (A-T) and mouse chromosomes (1-19 and sex) about 217 BESs (46.7% of 465 high homologous BESs). Twenty-three specific narrow regions in 13 chromosomes of the CHO DG44 cell line showed high homology to mouse chromosomes, but most of other regions did not show significant correlations with the mouse genome. These results contribute to accurate alignments of chromosomes of Chinese hamster and its genome sequence, analysis of chromosomal instability in CHO cells, and the development of target locations for gene and/or genome editing techniques.
中国仓鼠卵巢(CHO)细胞作为一种用于表达目的基因的哺乳动物宿主细胞平台,在生物技术领域中被广泛应用。此前,我们通过荧光原位杂交(FISH)成像技术,以303个细菌人工染色体(BAC)克隆作为杂交探针(BAC-FISH),构建了CHO DG44细胞系的详细物理染色体图谱。BAC-FISH结果显示,两条最长的染色体完全配对。然而,其他染色体存在部分缺失或重排。在本研究中,我们确定了用于BAC-FISH探针的303个BAC克隆的末端序列(BAC末端序列)。在606个BAC末端序列(正向和反向末端)中,有558个可以确定。我们使用NCBI BLAST对所有确定的BAC末端序列与小鼠基因组序列进行了比较。在这558个BAC末端序列中,有465个与小鼠染色体序列具有高度同源性。我们利用物理染色体图谱分析了这些BAC在CHO DG44细胞系染色体中的位置。根据所得结果,我们研究了CHO染色体(A-T)与小鼠染色体(1-19和性染色体)中约217个BAC末端序列(465个高度同源BAC末端序列的46.7%)的区域相似性。CHO DG44细胞系13条染色体中的23个特定狭窄区域与小鼠染色体具有高度同源性,但其他大多数区域与小鼠基因组没有显著相关性。这些结果有助于准确比对中国仓鼠的染色体及其基因组序列,分析CHO细胞中的染色体不稳定性,以及开发基因和/或基因组编辑技术的目标定位。