Médigue C, Hénaut A, Danchin A
Atelier de Bioinformatique, Section Physique-Chimie, Institut Curie, Paris, France.
Mol Microbiol. 1990 Sep;4(9):1443-54.
The sequenced genes from Escherichia coli that are available in the EMBL library (release 21) have been localized on an updated and corrected version of the restriction map of the chromosome generated by Kohara et al. (1987). One thousand kbp of sequenced DNA are incorporated in this update; this is equivalent to 23% of the total genome. The accuracy of the map is assessed, and it is corrected and updated where appropriate. A significant number of sites were missing from the original map, mainly involving two of the eight enzymes used by Kohara et al. (1987), ie. PvuII and EcoRV. The nucleotide environment of such missing sites was examined and, using an Artificial Intelligence approach, it appears that the site for these enzymes is sensitive to context effects. Several genes of known position on the E. coli chromosome could not be placed on the restriction map; this suggests that additional gaps are likely to exist on the restriction map, in addition to the original seven identified by Kohara et al. We have also obtained information about the probable direction of transcription of chromosomal genes with respect to the map. Most genes are transcribed in the same direction as the replication forks, particularly around oriC at 84 min.
来自大肠杆菌的已测序基因(可在EMBL文库第21版中获取)已定位在由小原等人(1987年)绘制的染色体限制性图谱的更新和校正版本上。此次更新纳入了1000kbp的已测序DNA;这相当于基因组总量的23%。对图谱的准确性进行了评估,并在适当之处进行了校正和更新。原始图谱中缺少大量位点,主要涉及小原等人(1987年)使用的八种酶中的两种,即PvuII和EcoRV。对这些缺失位点的核苷酸环境进行了研究,并且使用人工智能方法发现,这些酶的位点对上下文效应敏感。大肠杆菌染色体上一些已知位置的基因无法定位在限制性图谱上;这表明除了小原等人确定的原始七个缺口外,限制性图谱上可能还存在其他缺口。我们还获得了有关染色体基因相对于图谱可能的转录方向的信息。大多数基因与复制叉的转录方向相同,特别是在84分钟处的oriC周围。