Evidence map›Paper›PMID 36945655›Full record

ArticlebioRxiv : the preprint server for biology2023

Intragenic DNA inversions expand bacterial coding capacity.

Rachael B Chanin, Patrick T West, Ryan M Park, Jakob Wirbel, Gabriella Z M Green, Arjun M Miklos, Matthew O Gill, Angela S Hickey, Erin F Brooks, Ami S Bhatt

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors.

Rachael B ChaninDepartment of Medicine (Hematology, Blood and Marrow Transplantation); Stanford, USA.
Patrick T WestDepartment of Medicine (Hematology, Blood and Marrow Transplantation); Stanford, USA.
Ryan M ParkDepartment of Medicine (Hematology, Blood and Marrow Transplantation); Stanford, USA.
Jakob WirbelDepartment of Medicine (Hematology, Blood and Marrow Transplantation); Stanford, USA.
Gabriella Z M GreenDepartment of Medicine (Hematology, Blood and Marrow Transplantation); Stanford, USA.
Arjun M MiklosDepartment of Medicine (Hematology, Blood and Marrow Transplantation); Stanford, USA.
Matthew O GillDepartment of Genetics, Stanford University; Stanford, USA.
Angela S HickeyDepartment of Genetics, Stanford University; Stanford, USA.
Erin F BrooksDepartment of Medicine (Hematology, Blood and Marrow Transplantation); Stanford, USA.
Ami S BhattDepartment of Medicine (Hematology, Blood and Marrow Transplantation); Stanford, USA.

Funding

INSTITUTIONAL TRAINING GRANT IN GENOME SCIENCET32HG000044 · NHGRI · STANFORD UNIVERSITY · PI MICHAEL P. SNYDER · 1995 to 2026
$32.2M
Culture-free pathogen tracking in hospitalized patientsR01AI143757 · NIAID · STANFORD UNIVERSITY · PI BHATT, AMI SIDDHARTH · 2020 to 2023
$3.0M
Program in Translational and Experimental HematologyT32HL120824 · NHLBI · STANFORD UNIVERSITY · PI MAJETI, RAVINDRA · 2014 to 2023
$2.4M
Emerging novel mechanisms of antibiotic resistance in the prevalent foodborne pathogen, SalmonellaR01AI148623 · NIAID · STANFORD UNIVERSITY · PI BHATT, AMI SIDDHARTH · 2019 to 2023
$2.0M
COMPUTATIONAL METHODS FOR PROTEOMIC ANALYSISK22HG000044 · NHGRI · UNIVERSITY OF UTAH · PI GIDDINGS, MORGAN CORINNE · 2000 to 2005
$1.3M
NHGRI NIH HHS K22 HG000044NHGRI NIH HHS T32 HG000044NHLBI NIH HHS T32 HL120824NIAID NIH HHS R01 AI143757NIAID NIH HHS R01 AI148623
6 · The paper itself

Abstract

Bacterial populations that originate from a single bacterium are not strictly clonal. Often, they contain subgroups with distinct phenotypes. Bacteria can generate heterogeneity through phase variation: a preprogrammed, reversible mechanism that alters gene expression levels across a population. One well studied type of phase variation involves enzyme-mediated inversion of specific intergenic regions of genomic DNA. Frequently, these DNA inversions flip the orientation of promoters, turning ON or OFF adjacent coding regions within otherwise isogenic populations. Through this mechanism, inversion can affect fitness, survival, or group dynamics. Here, we develop and apply bioinformatic approaches to discover thousands of previously undescribed phase-variable regions in prokaryotes using long-read datasets. We identify 'intragenic invertons', a surprising new class of invertible elements found entirely within genes, in bacteria and archaea. To date, inversions within single genes have not been described. Intragenic invertons allow a gene to encode two or more versions of a protein by flipping a DNA sequence within the coding region, thereby increasing coding capacity without increasing genome size. We experimentally characterize specific intragenic invertons in the gut commensal

Identifiers

PMID36945655
PMCPMC10028968

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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 Socratic graph.