Evidence map›Paper›PMID 20226075›Full record

ArticleMobile DNA2010

Heads or tails: L1 insertion-associated 5' homopolymeric sequences.

Thomas J Meyer, Deepa Srikanta, Erin M Conlin, Mark A Batzer

Abstract read
In one paragraph

Article in Mobile DNA, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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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3 · Its place in the literature

Who cites it

6 citing papers in PubMed.

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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

4 authors.

Thomas J Meyer *Department of Biological Sciences, Biological Computation and Visualization Center, Louisiana State University, 202 Life Sciences Bldg, Baton Rouge, LA 70803, USA.
Deepa Srikanta *Department of Biological Sciences, Biological Computation and Visualization Center, Louisiana State University, 202 Life Sciences Bldg, Baton Rouge, LA 70803, USA.
Erin M ConlinDepartment of Biological Sciences, Biological Computation and Visualization Center, Louisiana State University, 202 Life Sciences Bldg, Baton Rouge, LA 70803, USA.
Mark A BatzerDepartment of Biological Sciences, Biological Computation and Visualization Center, Louisiana State University, 202 Life Sciences Bldg, Baton Rouge, LA 70803, USA.

Funding

POPULATION GENETICS OF MOBILE ELEMENTSR01GM059290 · NIGMS · UNIVERSITY OF UTAH · PI BATZER, MARK A, FESCHOTTE, CEDRIC · 1999 to 2018
$8.5M
NIGMS NIH HHS R01 GM059290
6 · The paper itself

Abstract

backgroundL1s are one of the most successful autonomous mobile elements in primate genomes. These elements comprise as much as 17% of primate genomes with the majority of insertions occurring via target primed reverse transcription (TPRT). Twin priming, a variant of TPRT, can result in unusual DNA sequence architecture. These insertions appear to be inverted, truncated L1s flanked by target site duplications.

resultsWe report on loci with sequence architecture consistent with variants of the twin priming mechanism and introduce dual priming, a mechanism that could generate similar sequence characteristics. These insertions take the form of truncated L1s with hallmarks of classical TPRT insertions but having a poly(T) simple repeat at the 5' end of the insertion. We identified loci using computational analyses of the human, chimpanzee, orangutan, rhesus macaque and marmoset genomes. Insertion site characteristics for all putative loci were experimentally verified.

conclusionsThe 39 loci that passed our computational and experimental screens probably represent inversion-deletion events which resulted in a 5' inverted poly(A) tail. Based on our observations of these loci and their local sequence properties, we conclude that they most probably represent twin priming events with unusually short non-inverted portions. We postulate that dual priming could, theoretically, produce the same patterns. The resulting homopolymeric stretches associated with these insertion events may promote genomic instability and create potential target sites for future retrotransposition events.

Identifiers

PMID20226075
PMCPMC2837659

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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.