Department of Physics, University of Pennsylvania, Philadelphia, PA 19104, USA.
Proc Natl Acad Sci U S A. 2012 May 8;109(19):7445-50. doi: 10.1073/pnas.1109479109. Epub 2012 Apr 23.
It has long been hypothesized that subcellular positioning of chromosomal loci in bacteria may be influenced by gene function and expression state. Here we provide direct evidence that membrane protein expression affects the position of chromosomal loci in Escherichia coli. For two different membrane proteins, we observed a dramatic shift of their genetic loci toward the membrane upon induction. In related systems in which a cytoplasmic protein was produced, or translation was eliminated by mutating the start codon, a shift was not observed. Antibiotics that block transcription and translation similarly prevented locus repositioning toward the membrane. We also found that repositioning is relatively rapid and can be detected at positions that are a considerable distance on the chromosome from the gene encoding the membrane protein (>90 kb). Given that membrane protein-encoding genes are distributed throughout the chromosome, their expression may be an important mechanism for maintaining the bacterial chromosome in an expanded and dynamic state.
长期以来,人们一直假设细菌中染色体基因座的亚细胞定位可能受到基因功能和表达状态的影响。在这里,我们提供了直接的证据表明膜蛋白的表达会影响大肠杆菌中染色体基因座的位置。对于两种不同的膜蛋白,我们观察到它们的遗传基因座在诱导时明显向膜移动。在相关的系统中,当细胞质蛋白产生或通过突变起始密码子消除翻译时,没有观察到这种移动。阻断转录和翻译的抗生素也同样阻止了基因座向膜的重新定位。我们还发现,重新定位相对较快,并且可以在距编码膜蛋白的基因有相当大距离的染色体位置上检测到(>90 kb)。鉴于膜蛋白编码基因分布在整个染色体上,它们的表达可能是维持细菌染色体处于扩展和动态状态的重要机制。