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Evidence for a new form of retroviral env transcript in leukemic and normal mouse lymphoid cells

Journal Article · · J. Virol.; (United States)
OSTI ID:5653242
Murine leukemia virus-related RNA species were examined in a set of radiation-induced T-cell leukemias from BALB/c mice. No evidence was found for linkage of viral long terminal repeat-derived (U5) sequences to information of host origin. A novel class of 2-kilobase (kb) env-related transcripts, about 1kb shorter than normal viral env messenger, was found in all the leukemias. All of the 2-kb transcripts contained sequences homologous to the xenotropic virus-related env sequences in the Friend spleen focus-forming virus, representing the N-terminal portion of gp70. In two of the leukemias, these transcripts were found to contain both ecotropic p15E and U3 sequences in addition to the xenotropic gp70-related sequence. These two leukemias, but not others in which ecotropic sequences were absent from the 2-kb RNA, harbored several copies of a specific class of env recombinant proviruses. These proviruses possessed full-size env genes and were submethylated, as shown by SmaI and XmaI digests of proviral DNA. Low levels of 2-kb RNA were found in normal thymocytes from strains BALB/c, AKR, and 129 but not from congenic 129 GIX- mice. It is possible that the 2-kb RNA may originate by a novel splicing step that removes portions of the gp70 and p15E sequences from full-length env transcripts.
Research Organization:
Memorial Sloan-Kettering Cancer Center, Cornell University Graduate School of Medical Sciences, New York, New York
OSTI ID:
5653242
Journal Information:
J. Virol.; (United States), Journal Name: J. Virol.; (United States) Vol. 48:1; ISSN JOVIA
Country of Publication:
United States
Language:
English