Unknown

Dataset Information

0

Restricting conformational flexibility of the switch II region creates a dominant-inhibitory phenotype in Obg GTPase Nog1.


ABSTRACT: Nog1 is a conserved eukaryotic GTPase of the Obg family involved in the biogenesis of 60S ribosomal subunits. Here we report the unique dominant-inhibitory properties of a point mutation in the switch II region of mouse Nog1; this mutation is predicted to restrict conformational mobility of the GTP-binding domain. We show that although the mutation does not significantly affect GTP binding, ectopic expression of the mutant in mouse cells disrupts productive assembly of pre-60S subunits and arrests cell proliferation. The mutant impairs processing of multiple pre-rRNA intermediates, resulting in the degradation of the newly synthesized 5.8S/28S rRNA precursors. Sedimentation analysis of nucleolar preribosomes indicates that defective Nog1 function inhibits the conversion of 32S pre-rRNA-containing complexes to a smaller form, resulting in a drastic accumulation of enlarged pre-60S particles in the nucleolus. These results suggest that conformational changes in the switch II element of Nog1 have a critical importance for the dissociation of preribosome-bound factors during intranucleolar maturation and thereby strongly influence the overall efficiency of the assembly process.

SUBMITTER: Lapik YR 

PROVIDER: S-EPMC2169037 | biostudies-literature | 2007 Nov

REPOSITORIES: biostudies-literature

altmetric image

Publications

Restricting conformational flexibility of the switch II region creates a dominant-inhibitory phenotype in Obg GTPase Nog1.

Lapik Yevgeniya R YR   Misra Julia M JM   Lau Lester F LF   Pestov Dimitri G DG  

Molecular and cellular biology 20070904 21


Nog1 is a conserved eukaryotic GTPase of the Obg family involved in the biogenesis of 60S ribosomal subunits. Here we report the unique dominant-inhibitory properties of a point mutation in the switch II region of mouse Nog1; this mutation is predicted to restrict conformational mobility of the GTP-binding domain. We show that although the mutation does not significantly affect GTP binding, ectopic expression of the mutant in mouse cells disrupts productive assembly of pre-60S subunits and arres  ...[more]

Similar Datasets

| S-EPMC6925385 | biostudies-literature
| S-EPMC4195776 | biostudies-literature
| S-EPMC4743925 | biostudies-literature
| S-EPMC6968927 | biostudies-literature
| S-EPMC5569028 | biostudies-literature
| S-EPMC4028186 | biostudies-literature
| S-EPMC4487204 | biostudies-literature
| S-EPMC5431965 | biostudies-literature
| S-EPMC4907111 | biostudies-literature
| S-EPMC8064090 | biostudies-literature