Evidence map›Paper›PMID 15516563›Full record

ArticleJournal of bacteriology2004

Sequence organization and insertion specificity of the novel chimeric ISHp609 transposable element of Helicobacter pylori.

Dangeruta Kersulyte, Awdhesh Kalia, MaoJun Zhang, Hae-Kyung Lee, Dharmalingam Subramaniam, Levute Kiuduliene, Henrikas Chalkauskas, Douglas E Berg

Open access · greenAbstract read
In one paragraph

Article in Journal of bacteriology, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
0.6field-weighted citation impact, top 27% 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

18 citing papers in PubMed, 23 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Mechanisms of DNA Transposition.Microbiology spectrum · 2015
    Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Recombination and DNA repair in Helicobacter pylori.Annual review of microbiology · 2011
    Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. 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

8 authors at 4 institutions in 4 countries.

Dangeruta KersulyteDepartment of Molecular Microbiology, Washington University School of Medicine, St. Louis, MO 63110, USA.
Awdhesh Kalia
MaoJun Zhang
Hae-Kyung Lee
Dharmalingam Subramaniam
Levute Kiuduliene
Henrikas Chalkauskas
Douglas E Berg
Washington University in St. Louis · USCzech Academy of Sciences, Institute of Biotechnology · CZThe Catholic University of Korea Uijeongbu St. Mary's Hospital · KRVilnius University · LT

Funding

Washington University DDRCC Supplemental Equipment RequestP30DK052574 · NIDDK · WASHINGTON UNIVERSITY · PI Nicholas O. Davidson · 2000 to 2026
$30.8M
H.PYLORI POPULATION GENETICS AND GENOME EVOLUTIONR01DK063041 · NIDDK · WASHINGTON UNIVERSITY · PI BERG, DOUGLAS EUGENE · 2003 to 2007
$1.6M
H. PYLORI INFECTION AND GI DISEASE IN ALASKA NATIVESR01DK053727 · NIDDK · WASHINGTON UNIVERSITY · PI BERG, DOUGLAS EUGENE · 1999 to 2003
$1.3M
DRUG RESISTANCE AND GENE TRANSFER IN H PYLORIR01AI038166 · NIAID · WASHINGTON UNIVERSITY · PI BERG, DOUGLAS EUGENE · 1995 to 2003
$1.1M
Molecular Genetics of H. Pylori In IndiaR03AI049161 · NIAID · WASHINGTON UNIVERSITY · PI BERG, DOUGLAS EUGENE · 2000 to 2002
$222k
NIAID NIH HHS R01 AI38166NIAID NIH HHS R03 AI49161NIDDK NIH HHS P30 DK052574NIDDK NIH HHS P30 DK52574NIDDK NIH HHS R01 DK063041NIDDK NIH HHS R01 DK53727NIDDK NIH HHS R01 DK63041
6 · The paper itself

Abstract

Here we describe ISHp609 of Helicobacter pylori, a new member of the IS605 mobile element family that is novel and contains two genes whose functions are unknown, jhp960 and jhp961, in addition to homologs of two other H. pylori insertion sequence (IS) element genes, orfA, which encodes a putative serine recombinase-transposase, and orfB, whose homologs in other species are also often annotated as genes that encode transposases. The complete four-gene element was found in 10 to 40% of strains obtained from Africa, India, Europe, and the Americas but in only 1% of East Asian strains. Sequence comparison of 10 representative ISHp609 elements revealed higher levels of DNA sequence matches (99%) than those seen in normal chromosomal genes (88 to 98%) or in other IS elements (95 to 97% for IS605, IS606, and IS607) from the same H. pylori populations. Sequence analysis suggested that ISHp609 can insert at many genomic sites with its left end preferentially next to TAT, with no target specificity for its right end, and without duplicating or deleting target sequences. A deleted form of ISHp609, containing just jhp960 and jhp961 and 37 bp of orfA, found in reference strain J99, was at the same chromosomal site in 15 to 40% of the strains from many geographic regions but again in only 1% of the East Asian strains. The abundance and sequence homogeneity of ISHp609 and of this nonmobile remnant suggested a recent bottleneck and then rapid spread in H. pylori populations, possibly selected by the contributions of the elements to bacterial fitness.

Indexed as

AfricaAmericasAmino Acid SequenceAsiaBase SequenceDNA Transposable ElementsEuropeHelicobacter pyloriHumansMolecular Sequence DataOpen Reading FramesPhylogenyRecombinant Fusion ProteinsRecombinasesSequence Analysis, DNATransposasesDNA Transposable ElementsRecombinant Fusion ProteinsRecombinasesTransposases

Identifiers

PMID15516563
PMCPMC524915
OpenAlexW2016014825

What OpenQuestion holds

Textmetadata
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.