Abstract:
:NudC encodes a protein of unknown biochemical function that is required for nuclear migration. In an attempt to define its function by identifying interacting proteins, a screen for extragenic suppressors of the temperature-sensitive nudC3 mutation was undertaken that identified nine snc genes. Here we demonstrate that nudC3 has a missense mutation at amino acid 146 that causes leucine to be replaced by proline and that sncB69 encodes a mutant tRNA(Leu) that corrects the mutation. The sncB69 mutation deletes a single nucleotide in the anticodon of a tRNA(Leu) that changes its normal 5'CAG3' leucine anticodon to the proline anticodon 5'CCG3', which presumably allows incorporation of leucine at the mutant nudC3 proline codon 146 and thereby causes suppression of the nudC3 mutant phenotype.
journal_name
Geneticsjournal_title
Geneticsauthors
Chiu YH,Morris NRsubject
Has Abstractpub_date
1997-03-01 00:00:00pages
707-14issue
3eissn
0016-6731issn
1943-2631journal_volume
145pub_type
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