1. A PLPPV sequence in the p8 region of Gag provides late domain function for mouse mammary tumor virus.
- Author
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Coren LV, Nagashima K, and Ott DE
- Subjects
- Animals, Gene Products, gag chemistry, Gene Products, gag genetics, HEK293 Cells, Humans, Mammary Tumor Virus, Mouse chemistry, Mammary Tumor Virus, Mouse genetics, Mice, Microscopy, Electron, Amino Acid Motifs, Gene Products, gag metabolism, Mammary Tumor Virus, Mouse growth & development, Virus Release
- Abstract
The late (L) domain sequence used by mouse mammary tumor virus (MMTV) remains undefined. Similar to other L domain-containing proteins, MMTV p8 and p14
NC proteins are monoubiquitinated, suggesting L domain function. Site-directed mutagenesis of p8, PLPPV, and p14NC , PLPPL, sequences in MMTV Gag revealed a requirement only for the PLPPV sequence in virion release in a position-dependent manner. Electron microscopy of a defective Gag mutant confirmed an L domain budding defect morphology. The equine infectious anemia virus (EIAV) YPDL core L domain sequence and PLPPV provided L domain function in reciprocal MMTV and EIAV Gag exchange mutants, respectively. Alanine scanning of the PLPPV sequence revealed a strict requirement for the valine residue but only minor requirements for any one of the other residues. Thus, PLPPV provides MMTV L domain function, representing a fourth type of retroviral L domain that enables MMTV Gag proteins to co-opt cellular budding pathways for release., (Copyright © 2019 Elsevier Inc. All rights reserved.)- Published
- 2019
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