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Circularity of the Caulobacter crescentus chromosome determined by pulsed-field gel electrophoresis.

作者信息

Ely B, Ely T W, Gerardot C J, Dingwall A

机构信息

Department of Biological Sciences, University of South Carolina, Columbia 29208.

出版信息

J Bacteriol. 1990 Mar;172(3):1262-6. doi: 10.1128/jb.172.3.1262-1266.1990.

DOI:10.1128/jb.172.3.1262-1266.1990
PMID:2155197
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC208592/
Abstract

Previous genetic analyses of the Caulobacter crescentus chromosome have resulted in the construction of a linear genetic map. To establish the circularity of the C. crescentus chromosome, restriction fragments generated by digestion with AseI and SpeI were analyzed by pulsed-field gel electrophoresis and Southern hybridization. The size of each fragment was calculated and used to demonstrate that C. crescentus has a genome size of approximately 4,000 kilobases. In addition, both enzymes gave rise to large DNA fragments which contained genes from both ends of the genetic map. Thus, there is physical linkage between the genes at the ends of the genetic map and the chromosome is circular. Since this region of the chromosome appears to contain the replication terminus, we propose that recombination occurs at a high frequency in the vicinity of the terminus. This high frequency of recombination would prevent genetic linkage from being observed between genes on opposite sides of the terminus. Additional experiments using insertions which introduced new AseI and DraI restriction sites into the genome allowed us to calculate the physical distance between genes located in the vicinity of the replication terminus.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c1bb/208592/2a956dd5b83d/jbacter01045-0110-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c1bb/208592/674554bf7c14/jbacter01045-0109-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c1bb/208592/d6f20978e923/jbacter01045-0109-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c1bb/208592/2a956dd5b83d/jbacter01045-0110-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c1bb/208592/674554bf7c14/jbacter01045-0109-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c1bb/208592/d6f20978e923/jbacter01045-0109-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c1bb/208592/2a956dd5b83d/jbacter01045-0110-a.jpg

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本文引用的文献

1
Generalized Transduction in CAULOBACTER CRESCENTUS.新月弯孢菌的普遍性转导。
Genetics. 1977 Nov;87(3):391-9. doi: 10.1093/genetics/87.3.391.
2
Construction of a genetic map for Caulobacter crescentus.新月柄杆菌遗传图谱的构建。
J Bacteriol. 1982 Mar;149(3):889-96. doi: 10.1128/jb.149.3.889-896.1982.
3
Generation of a Tn5 promoter probe and its use in the study of gene expression in Caulobacter crescentus.Tn5启动子探针的构建及其在新月柄杆菌基因表达研究中的应用。
通过脉冲场凝胶电泳测定沃尔巴克氏体的基因组大小。
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4
Identification, characterization, and chromosomal organization of cell division cycle genes in Caulobacter crescentus.新月柄杆菌中细胞分裂周期基因的鉴定、表征及染色体组织
J Bacteriol. 1997 Apr;179(7):2169-80. doi: 10.1128/jb.179.7.2169-2180.1997.
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Physical mapping of bacterial genomes.细菌基因组的物理图谱
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6
Regulation of cellular differentiation in Caulobacter crescentus.新月柄杆菌中细胞分化的调控
Microbiol Rev. 1995 Mar;59(1):31-47. doi: 10.1128/mr.59.1.31-47.1995.
7
A physical map of the sulfur-dependent archaebacterium Sulfolobus acidocaldarius 7 chromosome.嗜热嗜酸硫化叶菌7号染色体的物理图谱。
J Bacteriol. 1993 Mar;175(5):1532-6. doi: 10.1128/jb.175.5.1532-1536.1993.
8
Organization of the bacterial chromosome.细菌染色体的组织
Microbiol Rev. 1990 Dec;54(4):502-39. doi: 10.1128/mr.54.4.502-539.1990.
9
Timing of flagellar gene expression in the Caulobacter cell cycle is determined by a transcriptional cascade of positive regulatory genes.柄杆菌细胞周期中鞭毛基因表达的时间由正调控基因的转录级联反应决定。
J Bacteriol. 1991 Feb;173(4):1514-22. doi: 10.1128/jb.173.4.1514-1522.1991.
10
A combined genetic and physical map of the Streptomyces coelicolor A3(2) chromosome.天蓝色链霉菌A3(2)染色体的遗传与物理联合图谱。
J Bacteriol. 1992 Sep;174(17):5496-507. doi: 10.1128/jb.174.17.5496-5507.1992.
Proc Natl Acad Sci U S A. 1984 Feb;81(4):1035-9. doi: 10.1073/pnas.81.4.1035.
4
Genetic mapping with Tn5-derived auxotrophs of Caulobacter crescentus.利用新月柄杆菌Tn5衍生的营养缺陷型进行基因定位。
J Bacteriol. 1982 Aug;151(2):888-98. doi: 10.1128/jb.151.2.888-898.1982.
5
Transposon mutagenesis in Caulobacter crescentus.新月柄杆菌中的转座子诱变
J Bacteriol. 1982 Feb;149(2):620-5. doi: 10.1128/jb.149.2.620-625.1982.
6
Cascade regulation of Caulobacter flagellar and chemotaxis genes.柄杆菌鞭毛和趋化性基因的级联调控
J Mol Biol. 1987 Mar 5;194(1):71-80. doi: 10.1016/0022-2836(87)90716-9.
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Vectors for transposon mutagenesis of non-enteric bacteria.用于非肠道细菌转座子诱变的载体。
Mol Gen Genet. 1985;200(2):302-4. doi: 10.1007/BF00425440.
8
Rate, origin, and bidirectionality of Caulobacter chromosome replication as determined by pulsed-field gel electrophoresis.
Proc Natl Acad Sci U S A. 1989 Jan;86(1):119-23. doi: 10.1073/pnas.86.1.119.
9
Use of pulsed-field-gradient gel electrophoresis to construct a physical map of the Caulobacter crescentus genome.使用脉冲场梯度凝胶电泳构建新月柄杆菌基因组的物理图谱。
Gene. 1988 Sep 7;68(2):323-33. doi: 10.1016/0378-1119(88)90035-2.
10
Order of gene replication in Caulobacter crescentus; use of in vivo labeled genomic DNA as a probe.新月柄杆菌中基因复制的顺序;使用体内标记的基因组DNA作为探针。
Mol Gen Genet. 1987 Dec;210(3):543-50. doi: 10.1007/BF00327210.