TY - JOUR
T1 - Repeated Chromosome Splitting Targeted to δ Sequences in Saccharomyces cerevisiae
AU - Sugiyama, Minetaka
AU - Nishizawa, Masafumi
AU - Hayashi, Kyouhei
AU - Kaneko, Yoshinobu
AU - Fukui, Kiichi
AU - Kobayashi, Akio
AU - Harashima, Satoshi
N1 - Funding Information:
Part of this work was financially supported by a grant from Bio-oriented Technology Research Advancement Institution (BRAIN), Japan and by the Ministry of Education, Culture, Sports, Science and Technology, a Grant-in-Aid for Scientific Research B, 12460044,200O to 2002, and carried out as part of the Project for the Development of a Technological Infrastructure for Industrial Bioprocesseso n R & D of New Industrial Sciencea nd Technology Frontiers by the Ministry of Economy, Trade and Industry (METI), and entrusted by the New Energy and Industrial Technology Development Organization (NEDO).
PY - 2003
Y1 - 2003
N2 - We have previously developed a chromosome-splitting technique based on homologous recombination in Saccharomyces cerevisiae. To facilitate chromosome splitting at multiple sites, we focused on the δ sequences that are distributed in more than 200 copies throughout the yeast genome. We constructed a new chromosome-splitting vector harboring the YFLWdelta4 sequence and the hisG-URA3-hisG cassette, and transformed yeast cells with this vector. The karyotype analysis of transformants showed that chromosomes XIV, III, and IV, or other chromosomes are split. After the excision of the URA3 gene, the transformant with split chromosome IV was subsequently transformed with the same vector. Karyotype analysis revealed that further splitting occurred at chromosome X, the split chromosome IV, or other chromosomes. These results indicate that δ sequences are efficient target sites for repeated chromosome splitting at multiple sites with a single vector.
AB - We have previously developed a chromosome-splitting technique based on homologous recombination in Saccharomyces cerevisiae. To facilitate chromosome splitting at multiple sites, we focused on the δ sequences that are distributed in more than 200 copies throughout the yeast genome. We constructed a new chromosome-splitting vector harboring the YFLWdelta4 sequence and the hisG-URA3-hisG cassette, and transformed yeast cells with this vector. The karyotype analysis of transformants showed that chromosomes XIV, III, and IV, or other chromosomes are split. After the excision of the URA3 gene, the transformant with split chromosome IV was subsequently transformed with the same vector. Karyotype analysis revealed that further splitting occurred at chromosome X, the split chromosome IV, or other chromosomes. These results indicate that δ sequences are efficient target sites for repeated chromosome splitting at multiple sites with a single vector.
KW - Chromosome engineering
KW - Genome
KW - Yeast
KW - δ repeated sequence
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U2 - 10.1263/jbb.96.397
DO - 10.1263/jbb.96.397
M3 - Article
C2 - 16233544
AN - SCOPUS:0345491336
SN - 1389-1723
VL - 96
SP - 397
EP - 400
JO - Journal of Bioscience and Bioengineering
JF - Journal of Bioscience and Bioengineering
IS - 4
ER -