Evidence map›Paper›PMID 14673549›Full record

ArticleImmunogenetics2004

Nucleotide sequencing analysis of the swine 433-kb genomic segment located between the non-classical and classical SLA class I gene clusters.

Atsuko Shigenari, Asako Ando, Christine Renard, Patrick Chardon, Takashi Shiina, Jerzy K Kulski, Hiroshi Yasue, Hidetoshi Inoko

Abstract readComparative Study
PubMed Publisher
In one paragraph

Article in Immunogenetics, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
4.8field-weighted citation impact, top 5% 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

10 citing papers in PubMed, 34 citations in OpenAlex.

  1. Article
  2. Article
  3. Identification of the high molecular weight isoform of phostensin.International journal of molecular sciences · 2014
    Article
  4. Article
  5. Immunolocalization of phostensin in lymphatic cells and tissues.The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society · 2011
    Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

8 authors at 4 institutions in 4 countries.

Atsuko ShigenariDepartment of Molecular Life Science, Tokai University School of Medicine, Bohseidai, Isehara, 259-1193, Kanagawa, Japan.
Asako Ando
Christine Renard
Patrick Chardon
Takashi Shiina
Jerzy K Kulski
Hiroshi Yasue
Hidetoshi Inoko
Tokai University · JPCommissariat à l'Énergie Atomique et aux Énergies Alternatives · FRInstitute of Agrobiological Sciences · JPInstitut National de la Recherche Agronomique · MA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Genome analysis of the swine leukocyte antigen ( SLA) region is needed to obtain information on the MHC genomic sequence similarities and differences between the swine and human, given the possible use of swine organs for xenotransplantation. Here, the genomic sequences of a 433-kb segment located between the non-classical and classical SLA class I gene clusters were determined and analyzed for gene organization and contents of repetitive sequences. The genomic organization and diversity of this swine non-class I gene region was compared with the orthologous region of the human leukocyte antigen ( HLA) complex. The length of the fully sequenced SLA genomic segment was 433 kb compared with 595 kb in the corresponding HLA class I region. This 162-kb difference in size between the swine and human genomic segments can be explained by indel activity, and the greater variety and density of repetitive sequences within the human MHC. Twenty-one swine genes with strong sequence similarity to the corresponding human genes were identified, with the gene order from the centromere to telomere of HCR - SPR1 - SEEK1 - CDSN - STG - DPCR1 - KIAA1885 - TFIIH - DDR - IER3 - FLOT1 - TUBB - KIAA0170 - NRM - KIAA1949 - DDX16 - FLJ13158 - MRPS18B - FB19 - ABCFI - CAT56. The human SEEK1 and DPCR1 genes are pseudogenes in swine. We conclude that the swine non-class I gene region that we have sequenced is highly conserved and therefore homologous to the corresponding region located between the HLA-C and HLA-E genes in the human.

Indexed as

AnimalsContig MappingGene DuplicationHistocompatibility Antigens Class IHistocompatibility Antigens Class IIHLA AntigensHumansMajor Histocompatibility ComplexMolecular Sequence DataPseudogenesSequence Analysis, DNASequence Homology, Nucleic AcidSpecies SpecificitySwineHistocompatibility Antigens Class IHistocompatibility Antigens Class IIHLA Antigensswine leukocyte antigen

Identifiers

PMID14673549
OpenAlexW1983361793

What OpenQuestion holds

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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.