Somatic diversification of chicken immunoglobulin light chains by point mutations

Ruti Parvari, Etty Ziv, Frida Lantner, Dan Heller, Israel Schechter

Research output: Contribution to journalArticlepeer-review

48 Scopus citations

Abstract

The light-chain locus of chicken has 1 functional Vλ1 gene, 1 J gene, and 25 pseudo-Vλ-genes (where V = variable and J = joining). A major problem is which somatic mechanisms expand this extremely limited germ-line information to generate many different antibodies. Weill's group [Reynaud, C. A., Anquez, V., Grimal, H. & Weill, J. C. (1987) Cell 48, 379-388] has shown that the pseudo-Vλ-genes diversify the rearranged Vλ1 by gene conversion. Here we demonstrate that chicken light chains are further diversified by somatic point mutations and by Vλ1-J flexible joining. Somatic point mutations were identified in the J and 3′ noncoding DNA of rearranged light-chain genes of chicken. These regions were analyzed because point mutations in V′1 are obscured by gene conversion; the J and 3′ noncoding DNA are presented in one copy per haploid genome and are not subject to gene conversion. In rodents point mutations occur as frequently in the V-J coding regions as in the adjacent flanking DNA. Therefore, we conclude that somatic point mutations diversify the Vλ1 of chicken. The frequency (0-1%) and distribution of the mutations (decreasing in number with increased distance from the Vλ1 segment) in chicken were as observed in rodents. Sequence variability at the Vλ1-J junctions could be attributed to imprecise joining of the Vλ1 and J genes. The modification by gene conversion of rearranged Vλ1 genes in the bursa was similar in chicken aged 3 months (9.5%) or 3 weeks (9.1%) - i.e., gene conversion that generates the preimmune repertoire in the bursa seems to level off around 3 weeks of age. This preimmune repertoire can be further diversified by somatic point mutations that presumably lead to the formation of antibodies with increased affinity. A segment with structural features of a matrix association region [(A+T)-rich and four topoisomerase II binding sites] was identified in the middle of the J-Cλ intron (where C = constant).

Original languageEnglish
Pages (from-to)3072-3076
Number of pages5
JournalProceedings of the National Academy of Sciences of the United States of America
Volume87
Issue number8
DOIs
StatePublished - 1 Jan 1990
Externally publishedYes

Keywords

  • Gene conversion
  • Imprecise joining of variable and joining regions
  • Matrix association region
  • Preimmune antibody repertoire

Fingerprint

Dive into the research topics of 'Somatic diversification of chicken immunoglobulin light chains by point mutations'. Together they form a unique fingerprint.

Cite this