AKV is an endogenous, ecotropic murine leukemia virus that serves as one of the parents of the recombinant, oncogenic mink cell focus-forming viruses that arise in preleukemic AKR mice. I report the 8,374-nucleotide-long sequence of AKV, as determined from the infectious molecular clone AKR-623. The 5'-leader sequence of AKV extends to nucleotide 639, after which lies a long open reading frame encoding the gag and pol gene products. The reading frame is interrupted by a single amber codon separating the gag and pol genes. The pol gene overlaps the env gene within the 3' region of the AKV genome. The nucleotide sequence of the 5' region of AKV reveals the following features. (i) The 5'-leader sequence lacks any AUG codon to initiate translation of gPr8QW'-, suggesting that gPr8Yg'l is not required for the replication of AKV. (ii) A short portion of the leader region diverges in sequence from the closely related Moloney murine leukemia virus and appears to be related to a sequence highly repeated in eucaryotic genomes. (iii) As in Moloney murine leukemia virus, there is a potential RNA secondary structure flanking the amber codon that separates the gag and pol genes. This structure might function as a regulatory protein binding site that controls the relative levels of synthesis of the gag and pol precursors. The nucleotide sequence of the 3' region of AKV is compared with sequences reported previously from both infectious and noninfectious molecular clones of AKV.The murine leukemia virus (MLV) AKV resides in the germ line of AKR mice and is implicated in the high incidence of thymic leukemias that arise when these mice are 6 to 9 months old. AKV is expressed in AKR mice from birth (41) and is distinguished from the other MLV endogenous to AKR mice because it is ecotropic; i.e., it can infect mouse cells. Low-leukemic strains of mice (e.g., NIH/Swiss) which have acquired a germ line AKV provirus from AKR mice become viremic and subsequently contract leukemia, albeit with a considerably longer latency period (39,40). Nevertheless, AKV itself does not appear to be directly oncogenic because it is unable to induce leukemia in healthy mice (18,29).During the development of AKR mice, AKV recombines with germ line nonecotropic MLV to produce recombinant MLVs (4,5,9,17,19,23,38) not found in the germ line of AKR mice (3,17,36). The recombinants, called MCF, appear in the preleukemic thymus (14) and are thought to be the proximal oncogenic agent in AKR leukemogenesis because they can accelerate the onset of leukemia if injected into young AKR mice (6, 31), and they are found integrated in the genomes of leukemic thymocytes (3,16,36). Because the nonecotropic parent of MCF viruses has not been identified, the nonecotropic sequences within MCF genomes have been localized by comparison to AKV.The nucleotide sequence of the 3' region of the AKV genome has been reported previously. Lenz et al. (21) and Van Beveren et al. (56) determined the nucleotide sequence of the envelope (env) gene and the long terminal repeat (LTR), res...