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10.1016/j.mib.2014.09.014

http://scihub22266oqcxt.onion/10.1016/j.mib.2014.09.014
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C4258129!4258129!25305533
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suck abstract from ncbi


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pmid25305533      Curr+Opin+Microbiol 2014 ; ä (ä): 15-21
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  • New approaches to understanding the spatial organization of bacterial genomes #MMPMID25305533
  • Le TBK; Laub MT
  • Curr Opin Microbiol 2014[Dec]; ä (ä): 15-21 PMID25305533show ga
  • In all organisms, chromosomal DNA must be compacted nearly three orders of magnitude to fit within the limited volume of a cell. However, chromosomes cannot be haphazardly packed, and instead must adopt structures compatible with numerous cellular processes, including DNA replication, chromosome segregation, recombination, and gene expression. Recent technical advances have dramatically enhanced our understanding of how chromosomes are organized in vivo and have begun to reveal the mechanisms and forces responsible. Here, we review the current arsenal of techniques used to query chromosome structure, focusing on (i) single-cell fluorescence microscopy approaches that directly examine chromosome structure and (ii) population-averaged biochemical methods that infer chromosome structure based on the interaction frequencies of different chromosomal loci. We describe the power of these techniques, highlighting the major advances they have produced while also discussing their limitations.
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