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Carboxyl-terminal sequences influence the import of mitochondrial protein precursors in vivo.
- Source :
-
Proceedings of the National Academy of Sciences of the United States of America [Proc Natl Acad Sci U S A] 1987 Oct; Vol. 84 (19), pp. 6692-6. - Publication Year :
- 1987
-
Abstract
- The large subunit of carbamoyl phosphate synthase A [carbon-dioxide: L-glutamine amido-ligase (ADP-forming, carbamate-phosphorylating), EC 6.3.5.5] from Neurospora crassa is encoded by a nuclear gene but is localized in the mitochondrial matrix. We have utilized N. crassa strains that produce both normal and carboxyl-terminal-truncated forms of carbamoyl phosphate synthase A to ask whether the carboxyl terminus affects import of the carbamoyl phosphate synthase A precursor. We found that carboxyl-terminal-truncated precursors were directed to mitochondria but that they were imported less efficiently than full-length proteins that were synthesized in the same cytoplasm. Our results suggest that effective import of proteins into mitochondria requires appropriate combinations of targeting sequences and three-dimensional structure.
- Subjects :
- Amino Acid Sequence
Carbamoyl-Phosphate Synthase (Glutamine-Hydrolyzing) biosynthesis
Kinetics
Mutation
Neurospora crassa enzymology
Carbamoyl-Phosphate Synthase (Glutamine-Hydrolyzing) genetics
Ligases genetics
Mitochondria enzymology
Neurospora genetics
Neurospora crassa genetics
Protein Processing, Post-Translational
Subjects
Details
- Language :
- English
- ISSN :
- 0027-8424
- Volume :
- 84
- Issue :
- 19
- Database :
- MEDLINE
- Journal :
- Proceedings of the National Academy of Sciences of the United States of America
- Publication Type :
- Academic Journal
- Accession number :
- 2958846
- Full Text :
- https://doi.org/10.1073/pnas.84.19.6692