Evidence map›Paper›PMID 17720708›Full record

ArticleNucleic acids research2007

Altered target site specificity variants of the I-PpoI His-Cys box homing endonuclease.

Jennifer L Eklund, Umut Y Ulge, Jennifer Eastberg, Raymond J Monnat

Open access · goldAbstract read
In one paragraph

Article in Nucleic acids research, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.1field-weighted citation impact, top 24% 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

13 citing papers in PubMed, 22 citations in OpenAlex.

  1. Article
  2. Article
  3. Pest management by genetic addiction.Proceedings of the National Academy of Sciences of the United States of America · 2019
    Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Homing endonucleases: from basics to therapeutic applications.Cellular and molecular life sciences : CMLS · 2010
    Review
  12. Article
  13. Article
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 at 3 institutions in 1 country.

Jennifer L EklundDepartment of Genome Sciences, University of Washington, Seattle, WA, USA.
Umut Y Ulge
Jennifer Eastberg
Raymond J Monnat
University of Washington · USFred Hutch Cancer Center · USHuman Genome Sciences (United States) · US

Funding

University of Washington Medical Scientist Training Program: MD/PhDT32GM007266 · NIGMS · UNIVERSITY OF WASHINGTON · PI HORWITZ, MARSHALL S. · 1985 to 2023
$30.4M
TRAINING IN MOLECULAR AND CELLULAR BIOLOGYT32GM007270 · NIGMS · UNIVERSITY OF WASHINGTON · PI RAIBLE, DAVID W · 1985 to 2020
$21.0M
Interdisciplinary Tranining in Cancer ResearchT32CA080416 · NCI · UNIVERSITY OF WASHINGTON · PI STODDARD, BARRY L. · 1998 to 2023
$9.7M
TRAINING PROGRAM IN GENETICS GENERAL AND MEDICALT32GM007735 · NIGMS · UNIVERSITY OF WASHINGTON · PI THOMAS, JAMES H · 1985 to 2009
$3.8M
NOVEL HUMAN GENE SPECIFIC REAGENTS FROM HOMING ENDOSR01CA088942 · NCI · UNIVERSITY OF WASHINGTON · PI MONNAT, RAYMOND J · 2001 to 2005
$1.3M
NCI NIH HHS R01 CA088942NCI NIH HHS R01 CA88942NCI NIH HHS T32 CA077116NCI NIH HHS T32 CA080416NIGMS NIH HHS T32 GM007266NIGMS NIH HHS T32 GM007270NIGMS NIH HHS T32 GM007735NIGMS NIH HHS T32 GM07270NIGMS NIH HHS T32 GM07735
6 · The paper itself

Abstract

We used a yeast one-hybrid assay to isolate and characterize variants of the eukaryotic homing endonuclease I-PpoI that were able to bind a mutant, cleavage-resistant I-PpoI target or 'homing' site DNA in vivo. Native I-PpoI recognizes and cleaves a semi-palindromic 15-bp target site with high specificity in vivo and in vitro. This target site is present in the 28S or equivalent large subunit rDNA genes of all eukaryotes. I-PpoI variants able to bind mutant target site DNA had from 1 to 8 amino acid substitutions in the DNA-protein interface. Biochemical characterization of these proteins revealed a wide range of site-binding affinities and site discrimination. One-third of variants were able to cleave target site DNA, but there was no systematic relationship between site-binding affinity and site cleavage. Computational modeling of several variants provided mechanistic insight into how amino acid substitutions that contact, or are adjacent to, specific target site DNA base pairs determine I-PpoI site-binding affinity and site discrimination, and may affect cleavage efficiency.

Indexed as

DNA, RibosomalEndodeoxyribonucleasesGene LibraryModels, MolecularMutagenesis, Site-DirectedSubstrate SpecificityTwo-Hybrid System TechniquesDNA, RibosomalEndodeoxyribonucleasesI-Ppo endonuclease

Identifiers

PMID17720708
PMCPMC2034468
OpenAlexW2076574292

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.