Evidence map›Paper›PMID 23098210›Full record

ArticleBiology direct2012

Distinct groups of repetitive families preserved in mammals correspond to different periods of regulatory innovations in vertebrates.

Jerzy Jurka, Weidong Bao, Kenji K Kojima, Oleksiy Kohany, Matthew G Yurka

Open access · goldAbstract read
In one paragraph

Article in Biology direct, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.4field-weighted citation impact, top 11% of its field
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

14 citing papers in PubMed, 30 citations in OpenAlex.

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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 at 1 institution in 1 country.

Jerzy JurkaGenetic Information Research Institute, Mountain View, CA 94043, USA. jurka@girinst.org
Weidong Bao
Kenji K Kojima
Oleksiy Kohany
Matthew G Yurka
Genetic Information Research Institute · US

Funding

Rephase Update-a Database of Repetitive SequencesP41LM006252 · NLM · GENETIC INFORMATION RESEARCH INSTITUTE · PI JURKA, JERZY WLADYSLAW · 1996 to 2013
$6.0M
NLM NIH HHS 5 P41 LM006252
6 · The paper itself

Abstract

backgroundMammalian genomes are repositories of repetitive DNA sequences derived from transposable elements (TEs). Typically, TEs generate multiple, mostly inactive copies of themselves, commonly known as repetitive families or families of repeats. Recently, we proposed that families of TEs originate in small populations by genetic drift and that the origin of small subpopulations from larger populations can be fueled by biological innovations.

resultsWe report three distinct groups of repetitive families preserved in the human genome that expanded and declined during the three previously described periods of regulatory innovations in vertebrate genomes. The first group originated prior to the evolutionary separation of the mammalian and bird lineages and the second one during subsequent diversification of the mammalian lineages prior to the origin of eutherian lineages. The third group of families is primate-specific.

conclusionsThe observed correlation implies a relationship between regulatory innovations and the origin of repetitive families. Consistent with our previous hypothesis, it is proposed that regulatory innovations fueled the origin of new subpopulations in which new repetitive families became fixed by genetic drift.

Indexed as

Consensus SequenceDNA Transposable ElementsEvolution, MolecularGenomeAnimalsBirdsGenome, HumanHumansInterspersed Repetitive SequencesMammalsPrimatesSequence Analysis, DNAVertebratesDNA Transposable Elements

Identifiers

PMID23098210
PMCPMC3500645
OpenAlexW2096922346

What OpenQuestion holds

Textmetadata
LicenceCC BY
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 OpenQuestion graph.