Sj. Berens et al., USE OF A SINGLE V-H FAMILY AND LONG CDR3S IN THE VARIABLE REGION OF CATTLE IG HEAVY-CHAINS, International immunology, 9(1), 1997, pp. 189-199
We have analyzed transcripts encoding the variable regions of Ig heavy
chains from adult and fetal bovine splenocytes and bovine x mouse het
erohybridomas, The 13 adult, seven fetal and two heterohybridomas tran
scripts as well as the six genes that were sequenced had >83% identity
to each other in the V-H-encoded regions (FRs 1-3 and CDRs 1 and 2),
By this criterion, all the bovine sequences were assigned to one famil
y, which corresponds to the bovine homolog of the murine Q52 family. S
outhern blot analysis of genomic DNA demonstrated that homologs of oth
er murine V-H families such as 7183, S107 and 36-60 were present in th
e genome, but transcripts from these families were not detected in rap
id amplification of cDNA ends (RACE)-PCR amplified products or in indi
vidual clones. The sequences of the adult transcripts using the mu iso
type showed extensive somatic mutation indicating that the process of
somatic hypermutation begins earlier in development of the bovine B ce
ll. The length of CDR3 from V(D)J rearrangements averaged 21 amino aci
ds, which is larger than other mammalian CDR3s. Analysis of CDR3s from
23 fetal transcripts revealed a preference for a reading frame in the
putative D genes which is rich in glycine and tyrosine, and is also e
xtensively mutated in adults. The bovine immune system appears to util
ize Ig VH genes of a single family, but generates antibody diversity b
y extensive somatic mutation and long CDR3s which are subsequently hyp
ermutated.