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The PRC-barrel domain of the ribosome maturation protein RimM mediates binding to ribosomal protein S19 in the 30S ribosomal subunits

Lövgren, Mattias (author)
Umeå universitet,Institutionen för molekylärbiologi (Teknisk-naturvetenskaplig fakultet)
Bylund, Göran (author)
Umeå universitet,Institutionen för molekylärbiologi (Medicinska fakulteten)
Srivastava, Manoj (author)
Swedish University of Agricultural Sciences, Department of Forest Genetics and Plant Physiology
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Lundberg, Carina (author)
Umeå universitet,Institutionen för molekylärbiologi (Teknisk-naturvetenskaplig fakultet)
Persson, Olof (author)
Umeå universitet,Institutionen för molekylärbiologi (Teknisk-naturvetenskaplig fakultet)
Wingsle, Gunnar (author)
Swedish University of Agricultural Sciences, Department of Forest Genetics and Plant Physiology
Wikström, Mikael (author)
Umeå universitet,Institutionen för molekylärbiologi (Teknisk-naturvetenskaplig fakultet),Wikström
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 (creator_code:org_t)
2004-10-20
2004
English.
In: RNA. - : Cold Spring Harbor Laboratory Press (CSHL). - 1355-8382 .- 1469-9001. ; 10:11, s. 1798-1812
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • The RimM protein in Escherichia coli is associated with free 30S ribosomal subunits but not with 70S ribosomes. A DeltarimM mutant is defective in 30S maturation and accumulates 17S rRNA. To study the interaction of RimM with the 30S and its involvement in 30S maturation, RimM amino acid substitution mutants were constructed. A mutant RimM (RimM-YY-->AA), containing alanine substitutions for two adjacent tyrosines within the PRC beta-barrel domain, showed a reduced binding to 30S and an accumulation of 17S rRNA compared to wild-type RimM. The (RimM-YY-->AA) and DeltarimM mutants had significantly lower amounts of polysomes and also reduced levels of 30S relative to 50S compared to a wild-type strain. A mutation in rpsS, which encodes r-protein S19, suppressed the polysome- and 16S rRNA processing deficiencies of the RimM-YY-->AA but not that of the DeltarimM mutant. A mutation in rpsM, which encodes r-protein S13, suppressed the polysome deficiency of both rimM mutants. Suppressor mutations, found in either helices 31 or 33b of 16S rRNA, improved growth of both the RimM-YY-->AA and DeltarimM mutants. However, they suppressed the 16S rRNA processing deficiency of the RimM-YY-->AA mutant more efficiently than that of the DeltarimM mutant. Helices 31 and 33b are known to interact with S13 and S19, respectively, and S13 is known to interact with S19. A GST-RimM but not a GST-RimM(YY-->AA) protein bound strongly to S19 in 30S. Thus, RimM likely facilitates maturation of the region of the head of 30S that contains S13 and S19 as well as helices 31 and 33b.

Subject headings

LANTBRUKSVETENSKAPER  -- Lantbruksvetenskap, skogsbruk och fiske -- Skogsvetenskap (hsv//swe)
AGRICULTURAL SCIENCES  -- Agriculture, Forestry and Fisheries -- Forest Science (hsv//eng)
NATURVETENSKAP  -- Biologi -- Biokemi och molekylärbiologi (hsv//swe)
NATURAL SCIENCES  -- Biological Sciences -- Biochemistry and Molecular Biology (hsv//eng)

Keyword

Alanine/metabolism
Amino Acid Sequence
Amino Acid Substitution
Bacterial Proteins/*chemistry/genetics/*metabolism
Escherichia coli/genetics/growth & development
Escherichia coli Proteins/*chemistry/genetics/*metabolism
Gene Expression Regulation; Bacterial
Glutathione Transferase/metabolism
Models; Molecular
Molecular Sequence Data
Mutagenesis; Site-Directed
Mutation
Protein Structure; Tertiary
RNA Processing; Post-Transcriptional
RNA; Ribosomal; 16S/genetics/metabolism
RNA-Binding Proteins
Recombinant Proteins/metabolism
Ribosomal Proteins/*chemistry/genetics/*metabolism
Ribosomes/*metabolism
Sequence Homology; Amino Acid
Tyrosine/metabolism
MEDICINE
MEDICIN

Publication and Content Type

ref (subject category)
art (subject category)

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