Asymmetrical progression of replication forks just after initiation on Mycoplasma capricolum chromosome revealed by two-dimensional gel electrophoresis
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作者:
Miyata, M
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机构:Department of Biology, Faculty of Science, Osaka City University, Sumiyoshi-ku
Miyata, M
Fukumura, T
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机构:Department of Biology, Faculty of Science, Osaka City University, Sumiyoshi-ku
Fukumura, T
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[1] Department of Biology, Faculty of Science, Osaka City University, Sumiyoshi-ku
Previously, we mapped the replication initiation site of the Mycoplasma capricolum chromosome into a region containing the dnaA gene [M. Miyata et al., 1993a. Nucleic Acids Res. 21, 4816-4823]. In this study, various regions including this functional domain were analyzed by two complementary two-dimensional (2D) gel electrophoretic methods. Sizes of nascent strands in a 10.7-kb and a 5.6-kb region were examined by a neutral/alkaline (N/A) method. The shortest nascent strand was detected in an 875-bp region composed of the 3' end of the dnaA gene and its downstream non-coding sequence. The shortest nascent strand detected became longer in an asymmetrical manner as position of the probe became further from the putative initiation site in both directions. The intermediate forms of eight regions restricted at different sites were examined by a neutral/neutral (N/N) method. Bubble arcs were observed in four regions including the 875-bp region. The region containing the 875-bp region at about its center showed an asymmetrical are, although that containing the 875-bp region at its end showed a symmetrical are. These results show that the replication forks develop in the 875-bp region and proceed bidirectionally in an asymmetrical manner around the initiation site. The results of N/A analysis of the 5.6-kb region showed a shift of intensity in the nascent strand signal, which suggests an upshift of fork progression velocity. (C) 1997 Elsevier Science B.V.
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Hong Kong Polytech Univ, Dept Appl Biol & Chem Technol, Proteom Task Force, Kowloon, Hong Kong, Peoples R ChinaHong Kong Polytech Univ, Dept Appl Biol & Chem Technol, Proteom Task Force, Kowloon, Hong Kong, Peoples R China
Wang, YY
Cheung, PY
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Hong Kong Polytech Univ, Dept Appl Biol & Chem Technol, Proteom Task Force, Kowloon, Hong Kong, Peoples R ChinaHong Kong Polytech Univ, Dept Appl Biol & Chem Technol, Proteom Task Force, Kowloon, Hong Kong, Peoples R China
Cheung, PY
Wong, MS
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Hong Kong Polytech Univ, Dept Appl Biol & Chem Technol, Proteom Task Force, Kowloon, Hong Kong, Peoples R ChinaHong Kong Polytech Univ, Dept Appl Biol & Chem Technol, Proteom Task Force, Kowloon, Hong Kong, Peoples R China
Wong, MS
Lo, SCL
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Hong Kong Polytech Univ, Dept Appl Biol & Chem Technol, Proteom Task Force, Kowloon, Hong Kong, Peoples R ChinaHong Kong Polytech Univ, Dept Appl Biol & Chem Technol, Proteom Task Force, Kowloon, Hong Kong, Peoples R China
机构:Korea Res Inst Biosci & Biotechnol, System Proteom Res Ctr, Taejon 305600, South Korea
Kho, CW
Park, SG
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机构:Korea Res Inst Biosci & Biotechnol, System Proteom Res Ctr, Taejon 305600, South Korea
Park, SG
Lee, DH
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机构:Korea Res Inst Biosci & Biotechnol, System Proteom Res Ctr, Taejon 305600, South Korea
Lee, DH
Cho, SY
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机构:Korea Res Inst Biosci & Biotechnol, System Proteom Res Ctr, Taejon 305600, South Korea
Cho, SY
Oh, GT
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机构:Korea Res Inst Biosci & Biotechnol, System Proteom Res Ctr, Taejon 305600, South Korea
Oh, GT
Kang, SM
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机构:Korea Res Inst Biosci & Biotechnol, System Proteom Res Ctr, Taejon 305600, South Korea
Kang, SM
Park, BC
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Korea Res Inst Biosci & Biotechnol, System Proteom Res Ctr, Taejon 305600, South KoreaKorea Res Inst Biosci & Biotechnol, System Proteom Res Ctr, Taejon 305600, South Korea