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Journal ArticleDOI

Major reorganization of immunoglobulin VH segmental elements during vertebrate evolution.

K. Hinds, +3 more
- 01 Apr 1986 - 
- Vol. 320, Iss: 6062, pp 546-549
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TLDR
It is demonstrated that segmental reorganization involving mammalian-like DH and JH segments occurs in the lymphoid tissues of this species and may limit combinatorial joining and be a factor in the restricted antibody response of this lower vertebrate.
Abstract
In mammals, the immunoglobulin heavy-chain variable region (VH) locus is organized in a linear fashion; individual VH, diversity (DH), joining (JH) and constant (CH) region segments are linked in separate regions1. During somatic development, coding segments flanked by characteristic short recombination signal sequences, separated by intervening sequence regions that may exceed 2,000 kilobases (kb), are recombined. Combinatorial joining of different segments as well as imprecision in this process contribute to the diversity of the primary antibody response; subsequent mutation further alters functionally rearranged genes. This basic somatic reorganization mechanism is shared by six major families of genes encoding antigen receptors2. Previously, we have shown that multiple germline genes and mammalian-like recombination signal sequences are associated with the VH gene family of Heterodontus francisci (horned shark), a primitive elasmobranch3. Studies presented here demonstrate that segmental reorganization involving mammalian-like DH and JH segments occurs in the lymphoid tissues of this species. In marked contrast to the mammalian system, we find multiple instances of close linkage (∼10 kb) between individual VH, DH, JH and CH segments. This unique organization may limit combinatorial joining and be a factor in the restricted antibody response of this lower vertebrate4,5.

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Citations
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Origin and evolution of the adaptive immune system: genetic events and selective pressures

TL;DR: Insight is offered into the latest advances in this field of adaptive immune system research and speculate on the selective pressures that led to the emergence and maintenance of the AIS.
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Reconstructing immune phylogeny: new perspectives

TL;DR: Findings blur traditional distinctions between adaptive and innate immunity and emphasize that, throughout evolution, the immune system has used a remarkably extensive variety of solutions to meet fundamentally similar requirements for host protection.
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Comparative analyses of immunoglobulin genes: surprises and portents.

TL;DR: The study of immunoglobulin genes in non-mouse and non-human models has shown that different vertebrate groups have evolved distinct methods of generating antibody diversity, but the development of T cells in the thymus is quite similar in all of the species that have been examined.
Journal ArticleDOI

Evolution of antigen binding receptors.

TL;DR: Acquisition of large amounts of structural data for the antigen binding receptors that are found in a variety of jawed vertebrates has defined shared characteristics that provide unique insight into the distant origins of the rearranging gene systems and their relationships to both adaptive and innate recognition processes.
Journal ArticleDOI

Crystal Structure of a Shark Single-Domain Antibody V Region in Complex with Lysozyme

TL;DR: The 1.45 angstrom resolution crystal structure of the type I IgNAR V domain in complex with hen egg-white lysozyme (HEL) reveals a minimal antigen-binding domain that contains only two of the three conventional complementarity-determining regions but still binds HEL with nanomolar affinity by means of a binding interface comparable in size to conventional antibodies.
References
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Journal ArticleDOI

Somatic generation of antibody diversity

TL;DR: In the genome of a germ-line cell, the genetic information for an immunoglobulin polypeptide chain is contained in multiple gene segments scattered along a chromosome which are assembled by recombination which leads to the formation of a complete gene.
Journal ArticleDOI

Efficient isolation of genes by using antibody probes.

TL;DR: A sensitive and general technique has been devised for the dual purposes of cloning genes by using antibodies as probes and isolating unknown proteins encoded by cloned DNA using an expression vector that permits insertion of foreign DNA into the beta-galactosidase structural gene lacZ and promotes synthesis of hybrid proteins.
Journal ArticleDOI

Structure of the human immunoglobulin mu locus: characterization of embryonic and rearranged J and D genes.

TL;DR: The variable portion of an immunoglobulin heavy chain gene is assembled from at least three discontinuous segments of DNA, the V, D and J regions, and the large number of human J region genes and, hence, their greater potential for generating diversity as compared to the that of the mouse J regions appears to result from recent genetic duplications.
Journal ArticleDOI

An immunoglobulin heavy chain variable region gene is generated from three segments of DNA: VH, D and JH

TL;DR: A model for variable region gene rearrangement mediated by proteins which recognize the same conserved sequences adjacent to both light and heavy chain immunoglobulin gene segments is proposed.
Journal ArticleDOI

Joining of immunoglobulin heavy chain gene segments: implications from a chromosome with evidence of three D-JH fusions.

TL;DR: It is suggested that this added sequence is a product of the activity of terminal deoxynucleotidyltransferase at the D/JH (and probably the VH/D) joints and that it represents a new element of heavy chain gene structure, the N region.
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