PMID- 10627540 OWN - NLM STAT- MEDLINE DCOM- 20000207 LR - 20190508 IS - 0022-538X (Print) IS - 0022-538X (Linking) VI - 74 IP - 3 DP - 2000 Feb TI - Avian endogenous retrovirus EAV-HP shares regions of identity with avian leukosis virus subgroup J and the avian retrotransposon ART-CH. PG - 1296-306 AB - The existence of novel endogenous retrovirus elements in the chicken genome, designated EAV-HP, with close sequence identity to the env gene of avian leukosis virus (ALV) subgroup J has been reported (L. M. Smith, A. A. Toye, K. Howes, N. Bumstead, L. N. Payne, and K. Venugopal, J. Gen. Virol. 80:261-268, 1999). To resolve the genome structure of these retroviral elements, we have determined the complete sequence of two proviral clones of EAV-HP from a line N chicken genomic DNA yeast artificial chromosome library and from a meat-type chicken line 21 lambda library. The EAV-HP sequences from the two lines were 98% identical and had a typical provirus structure. The two EAV-HP clones showed identical large deletions spanning part of the gag, the entire pol, and part of the env genes. The env region of the EAV-HP clones was 97% identical to the env sequence of HPRS-103, the prototype subgroup J ALV. The 5' region of EAV-HP comprising the R and U5 regions of the long terminal repeat (LTR), the untranslated leader, and the 5' end of the putative gag region were 97% identical to the avian retrotransposon sequence, ART-CH. The remaining gag sequence shared less than 60% identity with other ALV sequences. The U3 region of the LTR was distinct from those of other retroviruses but contained some of the conserved motifs required for functioning as a promoter. To examine the ability of this endogenous retroviral LTR to function as a transcriptional promoter, the EAV-HP and HPRS-103 LTR U3 regions were compared in a luciferase reporter gene assay. The low luciferase activity detected with the EAV-HP LTR U3 constructs, at levels close to those observed for a control vector lacking the promoter or enhancer elements, suggested that these elements function as a weak promoter, possibly accounting for their low expression levels in chicken embryos. FAU - Sacco, M A AU - Sacco MA AD - Institute for Animal Health, Compton, Newbury, Berkshire RG20 7NN, United Kingdom. FAU - Flannery, D M AU - Flannery DM FAU - Howes, K AU - Howes K FAU - Venugopal, K AU - Venugopal K LA - eng SI - GENBANK/AJ238120 SI - GENBANK/AJ238121 SI - GENBANK/AJ238122 SI - GENBANK/AJ238123 SI - GENBANK/AJ238124 SI - GENBANK/AJ238125 PT - Journal Article PT - Research Support, Non-U.S. Gov't PL - United States TA - J Virol JT - Journal of virology JID - 0113724 RN - 0 (5' Untranslated Regions) RN - 0 (Retroelements) RN - 0 (Retroviridae Proteins) SB - IM MH - 5' Untranslated Regions/genetics MH - Amino Acid Motifs MH - Amino Acid Sequence MH - Animals MH - Avian Leukosis Virus/classification/*genetics MH - Base Sequence MH - Chick Embryo MH - Endogenous Retroviruses/*genetics MH - Gene Deletion MH - Genes, env/genetics MH - Genes, gag/genetics MH - Genes, pol/genetics MH - Molecular Sequence Data MH - Promoter Regions, Genetic MH - Proviruses/*genetics MH - Retroelements/*genetics MH - Retroviridae Proteins/chemistry/genetics MH - Sequence Alignment MH - Terminal Repeat Sequences/genetics MH - Transcription, Genetic PMC - PMC111464 EDAT- 2000/01/11 00:00 MHDA- 2000/01/11 00:01 CRDT- 2000/01/11 00:00 PHST- 2000/01/11 00:00 [pubmed] PHST- 2000/01/11 00:01 [medline] PHST- 2000/01/11 00:00 [entrez] AID - 10.1128/jvi.74.3.1296-1306.2000 [doi] PST - ppublish SO - J Virol. 2000 Feb;74(3):1296-306. doi: 10.1128/jvi.74.3.1296-1306.2000.