Published 2000 | Version public
Book Section - Chapter

New Approaches Towards an Understanding of Deuterostome Immunity

  • 1. ROR icon California Institute of Technology

Abstract

The vertebrate immune system is distinguished by an unusual propensity for genetic invention. For example, three forms of programmed somatic DNA recombination (V-D-J recombination, class switching and a highly targeted form of gene conversion) have arisen entirely independently in the course of immunoglobulin (Ig) heavy-chain gene evolution. Similar phenomena are virtually unknown in other metazoan genetic systems. Genes that mediate immunity are further characterized by accelerated sequence divergence rates when compared to nonimmune genes in studies of mouse and human gene orthologs (Hughes 1997; Murphy 1993). Both of these attributes, the tendency towards mechanistic novelty and a high rate of sequence evolution, may emerge from the dynamic nature of host-pathogen interactions and thus be a universal characteristic of immune systems. To investigate this possibility it is necessary to characterize immunity in animal phyla where the vertebrate forms of adaptive immunity are absent. A number of molecular advances have been made in recent years in the study of arthropod immunity (e.g., Hoffmann et al. 1996; Iwanaga and Kawabata 1998). As these data accumulate, in combination with similar work on an invertebrate deuterostome that is described here, a more general understanding of immunity will emerge.

Additional Information

© 2000 Springer-Verlag Berlin Heidelberg. We would like to thank M.K. Anderson for comments on the manuscript, K.J. Peterson for advice on metazoan phylogenetics. L.c. Smith for prepublication use of an S. purpuratus factor B probe and Paola Oliveri for help with the sea urchin PBX homeobox gene analysis. We also thank Jina Yun and Miki Yun for invaluable technical assistance. J.P.R. is supported by NIH Individual NRSA GM-18478. and Z.P. by NIH Training Grant HD-072S7.

Additional details

Identifiers

Eprint ID
64994
Resolver ID
CaltechAUTHORS:20160303-095639818

Funding

NIH
GM-18478
NIH
HD-072S7

Dates

Created
2016-03-04
Created from EPrint's datestamp field
Updated
2021-11-10
Created from EPrint's last_modified field

Caltech Custom Metadata

Series Name
Current Topics in Microbiology and Immunology
Series Volume or Issue Number
248