Evidence map›Paper›PMID 39501081›Full record

ArticleCommunications biology2024

Three-dimensional localization and tracking of chromosomal loci throughout the Escherichia coli cell cycle.

Praneeth Karempudi, Konrad Gras, Elias Amselem, Spartak Zikrin, Dvir Schirman, Johan Elf

Abstract read
In one paragraph

Article in Communications biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Praneeth Karempudi *Department of Cell and Molecular Biology, Science for Life Laboratory, Uppsala University, Husargatan 3, Uppsala, Uppsala, Sweden.ORCID 0000-0002-5925-8669
Konrad Gras *Department of Cell and Molecular Biology, Science for Life Laboratory, Uppsala University, Husargatan 3, Uppsala, Uppsala, Sweden.
Elias AmselemDepartment of Cell and Molecular Biology, Science for Life Laboratory, Uppsala University, Husargatan 3, Uppsala, Uppsala, Sweden.ORCID 0000-0003-2846-9225
Spartak ZikrinDepartment of Cell and Molecular Biology, Science for Life Laboratory, Uppsala University, Husargatan 3, Uppsala, Uppsala, Sweden.
Dvir SchirmanDepartment of Cell and Molecular Biology, Science for Life Laboratory, Uppsala University, Husargatan 3, Uppsala, Uppsala, Sweden.ORCID 0000-0001-5175-0176
Johan ElfDepartment of Cell and Molecular Biology, Science for Life Laboratory, Uppsala University, Husargatan 3, Uppsala, Uppsala, Sweden. johan.elf@icm.uu.se.ORCID 0000-0001-5522-1810

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The intracellular position of genes may impact their expression, but it has not been possible to accurately measure the 3D position of chromosomal loci. In 2D, loci can be tracked using arrays of DNA-binding sites for transcription factors (TFs) fused with fluorescent proteins. However, the same 2D data can result from different 3D trajectories. Here, we have developed a deep learning method for super-resolved astigmatism-based 3D localization of chromosomal loci in live E. coli cells which enables a precision better than 61 nm at a signal-to-background ratio of ~4 on a heterogeneous cell background. Determining the spatial localization of chromosomal loci, we find that some loci are at the periphery of the nucleoid for large parts of the cell cycle. Analyses of individual trajectories reveal that these loci are subdiffusive both longitudinally (x) and radially (r), but that individual loci explore the full radial width on a minute time scale.

Indexed as

Cell CycleChromosomes, BacterialEscherichia coliDeep LearningEscherichia coli ProteinsImaging, Three-DimensionalEscherichia coli Proteins

Identifiers

PMID39501081
PMCPMC11538341

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.