Bachmann B J
Department of Biology, Yale University, New Haven, Connecticut 06511-7444.
Microbiol Rev. 1990 Jun;54(2):130-97. doi: 10.1128/mr.54.2.130-197.1990.
The linkage map of Escherichia coli K-12 depicts the arrangement of genes on the circular chromosome of this organism. The basic units of the map are minutes, determined by the time-of-entry of markers from Hfr into F- strains in interrupted-conjugation experiments. The time-of-entry distances have been refined over the years by determination of the frequency of cotransduction of loci in transduction experiments utilizing bacteriophage P1, which transduces segments of DNA approximately 2 min in length. In recent years, the relative positions of many genes have been determined even more precisely by physical techniques, including the mapping of restriction fragments and the sequencing of many small regions of the chromosome. On the whole, the agreement between results obtained by genetic and physical methods has been remarkably good considering the different levels of accuracy to be expected of the methods used. There are now few regions of the map whose length is still in some doubt. In some regions, genetic experiments utilizing different mutant strains give different map distances. In other regions, the genetic markers available have not been close enough to give accurate cotransduction data. The chromosome is now known to contain several inserted elements apparently derived from lambdoid phages and other sources. The nature of the region in which the termination of replication of the chromosome occurs is now known to be much more complex than the picture given in the previous map. The present map is based upon the published literature through June of 1988. There are now 1,403 loci placed on the linkage group, which may represent between one-third and one-half of the genes in this organism.
大肠杆菌K-12的连锁图谱描绘了该生物体环形染色体上基因的排列情况。图谱的基本单位是分钟,通过中断杂交实验中标记从Hfr菌株进入F-菌株的时间来确定。多年来,通过利用噬菌体P1进行转导实验测定基因座共转导频率,对进入时间距离进行了细化,噬菌体P1可转导长度约为2分钟的DNA片段。近年来,通过物理技术,包括限制片段图谱绘制和染色体许多小区域的测序,许多基因的相对位置得到了更精确的确定。总体而言,考虑到所用方法预期的不同准确度水平,遗传方法和物理方法获得的结果之间的一致性非常好。现在图谱中仍有一些区域的长度存在疑问。在一些区域,利用不同突变菌株进行的遗传实验给出了不同的图谱距离。在其他区域,可用的遗传标记不够紧密,无法给出准确的共转导数据。现在已知染色体包含几个显然源自类λ噬菌体和其他来源的插入元件。现在已知染色体复制终止区域的性质比以前图谱中的情况要复杂得多。本图谱基于截至1988年6月的已发表文献。现在连锁群上有1403个基因座,它们可能代表该生物体中三分之一到二分之一的基因。