Transcription of germline V-H gene elements by normal human fetal liver

Transcription of the gene elements that form the variable region of immunoglobulin heavy chains has been proposed to represent the process that controls access for the recombination enzymes in their sequential steps of catalysis. Evidence for germline transcription of V-H gene elements, as part of V-H to DJ(H) recombination, has been limited to transcripts of only a few gene elements. We have examined normal fetal liver mRNA by Northern blotting and present evidence for germline transcripts from six human V-H gene families. The candidate V(H)4 transcripts have been confirmed as germline transcripts by hybridization with 3' flanking sequences that would have been removed by recombination from mature V(H)DJ(H) genes. The candidate transcripts for V(H)1, V(H)3, V(H)4 and V(H)6 have been confirmed by polymerase chain reaction amplification with primers from the 3' flanking sequences of these gene families and determination of the sequence of these products. Determination of sequence from two clones of VH 1, VH3 and VH4 indicates chat more than one gene from each of these families is transcribed. PCR amplification of VH4 and VH6 with primers specific for the leader sequence (exon 1) and 3' flanking sequence indicate that these transcripts are spliced, representing RNA processing. Germline transcripts from these families are also present in normal human bone marrow. These results indicate that transcriptional activation of germline V-H gene elements is a general phenomenon in tissues undergoing V to DJ recombination. (C) 1997 Published by Elsevier Science Ltd.