Evidence map›Paper›PMID 26338187›Full record

ArticleGenome biology and evolution2015

Combinatorial DNA Rearrangement Facilitates the Origin of New Genes in Ciliates.

Xiao Chen, Seolkyoung Jung, Leslie Y Beh, Sean R Eddy, Laura F Landweber

Abstract read
In one paragraph

Article in Genome biology and evolution, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing 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

21 citing papers in PubMed.

  1. A PIWI protein-dependent DNA N6-adenine methylation pathway inbioRxiv : the preprint server for biology · 2026
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  13. Evolutionary origins and impacts of genome architecture in ciliates.Annals of the New York Academy of Sciences · 2019
    Review
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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

5 authors.

Xiao ChenDepartment of Molecular Biology, Princeton University.
Seolkyoung JungJanelia Research Campus, Howard Hughes Medical Institute, Ashburn, Virginia.
Leslie Y BehDepartment of Ecology and Evolutionary Biology, Princeton University.
Sean R EddyJanelia Research Campus, Howard Hughes Medical Institute, Ashburn, Virginia Present address: Howard Hughes Medical Institute, Department of Molecular & Cellular Biology, and John A. Paulson School of Engineering and Applied Sciences, Harvard University.
Laura F LandweberDepartment of Ecology and Evolutionary Biology, Princeton University lfl@princeton.edu.

Funding

UNDERSTANDING COMPLEX GENE EDITING SYSTEMS IN PROTISTSR01GM059708 · NIGMS · PRINCETON UNIVERSITY · PI LANDWEBER, LAURA F · 1999 to 2016
$4.4M
RNA-guided Genome Rearrangement: Experiments Coupled with Discrete ModelsR01GM109459 · NIGMS · UNIVERSITY OF SOUTH FLORIDA · PI JONOSKA, NATASHA · 2013 to 2017
$2.0M
NIGMS NIH HHS GM109459NIGMS NIH HHS GM59708NIGMS NIH HHS R01 GM059708NIGMS NIH HHS R01 GM109459
6 · The paper itself

Abstract

Programmed genome rearrangements in the unicellular eukaryote Oxytricha trifallax produce a transcriptionally active somatic nucleus from a copy of its germline nucleus during development. This process eliminates noncoding sequences that interrupt coding regions in the germline genome, and joins over 225,000 remaining DNA segments, some of which require inversion or complex permutation to build functional genes. This dynamic genomic organization permits some single DNA segments in the germline to contribute to multiple, distinct somatic genes via alternative processing. Like alternative mRNA splicing, the combinatorial assembly of DNA segments contributes to genetic variation and facilitates the evolution of new genes. In this study, we use comparative genomic analysis to demonstrate that the emergence of alternative DNA splicing is associated with the origin of new genes. Short duplications give rise to alternative gene segments that are spliced to the shared gene segments. Alternative gene segments evolve faster than shared, constitutive segments. Genes with shared segments frequently have different expression profiles, permitting functional divergence. This study reports alternative DNA splicing as a mechanism of new gene origination, illustrating how the process of programmed genome rearrangement gives rise to evolutionary innovation.

Indexed as

Gene RearrangementAlternative SplicingBase SequenceCell NucleusComparative Genomic HybridizationDNA, ProtozoanEvolution, MolecularGene DuplicationGene Expression RegulationGenes, ProtozoanGerm CellsMolecular Sequence DataOxytrichaPhylogenySequence Analysis, DNASequence InversionDNA, Protozoanalternative splicingcomparative genomicsgene duplicationgenome rearrangementnovel genes

Identifiers

PMID26338187
PMCPMC4684698

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Registered trials

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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.