๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

Evolution of the Immune Repertoire with and without Somatic DNA Recombination

โœ Scribed by Katsuhisa Takumi; Pauline Hogeweg


Publisher
Elsevier Science
Year
1998
Tongue
English
Weight
197 KB
Volume
192
Category
Article
ISSN
0022-5193

No coin nor oath required. For personal study only.

โœฆ Synopsis


Repertoire of an immune system is a set of antigen receptors each having a unique specificity to bind an antigen. In many vertebrate species, antigen receptors are produced via combinatorial arrangements of DNA segments in specialized immune cells. Due to this molecular mechanism, repertoire of vertebrate species is potentially very large. The diversity of repertoire is thought to guarantee recognition of most ill-causing micro-organisms. In vertebrate species however, similar editing of DNA segments has not been demonstrated to take place. Immune system of invertebrate species therefore seems to operate in a distinct manner from that of vertebrate species. Using an evolutionary model in which organisms struggle to fight infections, we attempt to understand why some species use a more diverse set of antigen receptors than others. Individuals in our model either use somatic DNA recombination to produce antigen receptors (as in vertebrates) or do not use such a mechanism (as in vertebrates). We found that individuals having an invertebrate-like immune system came to employ only a few antigen receptors to recognize a set of pathogens whereas those with a vertebrate-like immune system use a larger set of more specific antigen receptors to recognize the same set of pathogens. Our interpretation of this finding is that because the genetics of the immune system imposed different constraints on the evolutionary process, two distinct recognition strategies have been adapted by these species.


๐Ÿ“œ SIMILAR VOLUMES


The evolution of meiosis: Recruitment an
โœ Edyta Marcon; Peter B. Moens ๐Ÿ“‚ Article ๐Ÿ“… 2005 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 393 KB ๐Ÿ‘ 2 views

Several DNA-damage detection and repair mechanisms have evolved to repair double-strand breaks induced by mutagens. Later in evolutionary history, DNA single- and double-strand cuts made possible immune diversity by V(D)J recombination and recombination at meiosis. Such cuts are induced endogenously

Theoretical Considerations of Cross-immu
โœ Mark M. Tanaka; Marcus W. Feldman ๐Ÿ“‚ Article ๐Ÿ“… 1999 ๐Ÿ› Elsevier Science ๐ŸŒ English โš– 240 KB

We explore the dynamics of multiple strains of a parasite in order to assess the conditions under which a novel strain, perhaps a mutant or migrant, may invade a population that already carries an endemic strain. Multiple strain dynamics can be modeled through coinfection, superinfection or complete

Structural evolution and flip-flop recom
โœ Diana B. Stein; Jeffrey D. Palmer; William F. Thompson ๐Ÿ“‚ Article ๐Ÿ“… 1986 ๐Ÿ› Springer-Verlag ๐ŸŒ English โš– 684 KB

The evolution and recombination of chloroplast genome structure in the fern genus Osmunda were studied by comparative restriction site mapping and filter hybridization of chloroplast DNAs (cpDNAs) from three species -O. cinnamomea, O. cIaytoniana and O. regalis. The three 144 kb circular genomes wer

The interaction of antibody/dna immune c
โœ Ronald P. Taylor; Jeffrey C. Edberg; Gregory A. Kujala; Andrew J. Sloman; Cara C ๐Ÿ“‚ Article ๐Ÿ“… 1987 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 967 KB

In 28 serum and plasma samples from patients with systemic lupus erythematosus, we examined the importance of antibody class with respect to complement-mediated binding to human red blood cells (RBC) of antibody/DNA immune complexes (IC) prepared with anti-DNA antibodies. We used both 3H-double-stra

Characterization of a human monoclonal a
โœ R.A. Heijtink; J. Kruining; P. van Bergen; S. de Rave; J. van Hattum; M. Schutte ๐Ÿ“‚ Article ๐Ÿ“… 2002 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 204 KB

A human monoclonal antibody type IgG4, designated 1Ff4, was obtained by Epstein Barr virus transformation of peripheral blood lymphocytes from a hepatitis B vaccinee (HB-VAX: plasmaderived vaccine) after one boost of yeast recombinant DNA derived vaccine (Engerix-B). 1Ff4 binds preferentially to HBs