Evidence map›Paper›PMID 18490746›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2008

The evolution of multiple isotypic IgM heavy chain genes in the shark.

Victor Lee, Jing Li Huang, Ming Fai Lui, Karolina Malecek, Yuko Ohta, Arne Mooers, Ellen Hsu

Erratum issuedOpen access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
2.5field-weighted citation impact, top 12% 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

19 citing papers in PubMed, 32 citations in OpenAlex.

  1. High-Throughput BLI for One-Step Anti-International journal of molecular sciences · 2026
    Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Fish Immunoglobulins.Biology · 2016
    Review
  10. Assembly and Expression of Shark Ig Genes.Journal of immunology (Baltimore, Md. : 1950) · 2016
    Review
  11. Biased Immunoglobulin Light Chain Gene Usage in the Shark.Journal of immunology (Baltimore, Md. : 1950) · 2015
    Article
  12. Article
  13. Article
  14. Article
  15. The multiple shark Ig H chain genes rearrange and hypermutate autonomously.Journal of immunology (Baltimore, Md. : 1950) · 2011
    Article
  16. Article
  17. Article
  18. Characterization of arrangement and expression of the T cell receptor gamma locus in the sandbar shark.Proceedings of the National Academy of Sciences of the United States of America · 2009
    Article
  19. Article
4 · The record

Corrections and comments

  • Erratum issued
5 · Who and what money

Authors and funding

7 authors at 3 institutions in 2 countries.

Victor LeeDepartment of Physiology and Pharmacology, State University of New York Health Science Center, Brooklyn, NY 11203, USA.
Jing Li Huang
Ming Fai Lui
Karolina Malecek
Yuko Ohta
Arne Mooers
Ellen Hsu
State University of New York · USSimon Fraser University · CAUniversity of Maryland, Baltimore · US

Funding

Isotype Exclusion and Hypermutation in the Nurse SharkR01GM068095 · NIGMS · SUNY DOWNSTATE MEDICAL CENTER · PI HSU, ELLEN · 2004 to 2017
$3.1M
NIGMS NIH HHS GM068095NIGMS NIH HHS R01 GM068095
6 · The paper itself

Abstract

The IgM H chain gene organization of cartilaginous fishes consists of 15-200 miniloci, each with a few gene segments (V(H)-D1-D2-J(H)) and one C gene. This is a gene arrangement ancestral to the complex IgH locus that exists in all other vertebrate classes. To understand the molecular evolution of this system, we studied the nurse shark, which has relatively fewer loci, and characterized the IgH isotypes for organization, functionality, and the somatic diversification mechanisms that act upon them. Gene numbers differ slightly between individuals ( approximately 15), but five active IgM subclasses are always present. Each gene undergoes rearrangement that is strictly confined within the minilocus; in B cells there is no interaction between adjacent loci located > or =120 kb apart. Without combinatorial events, the shark IgM H chain repertoire is based on junctional diversity and, subsequently, somatic hypermutation. We suggest that the significant contribution by junctional diversification reflects the selected novelty introduced by RAG in the early vertebrate ancestor, whereas combinatorial diversity coevolved with the complex translocon organization. Moreover, unlike other cartilaginous fishes, there are no germline-joined VDJ at any nurse shark mu locus, and we suggest that such genes, when functional, are species-specific and may have specialized roles. With an entire complement of IgM genes available for the first time, phylogenetic analyses were performed to examine how the multiple Ig loci evolved. We found that all domains changed at comparable rates, but V(H) appears to be under strong positive selection for increased amino acid sequence diversity, and surprisingly, so does Cmicro2.

Indexed as

Evolution, MolecularGene Rearrangement, B-Lymphocyte, Heavy ChainGenes, Immunoglobulin Heavy ChainAnimalsBase SequenceGenesImmunoglobulin Heavy ChainsImmunoglobulin MMolecular Sequence DataPhylogenySequence AlignmentSharksImmunoglobulin Heavy ChainsImmunoglobulin M

Identifiers

PMID18490746
PMCPMC2590587
OpenAlexW1677824387

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.