Literature DB >> 2431717

Cytoskeleton involvement in the distribution of mRNP complexes and small cytoplasmic RNAs.

R C Bird, B H Sells.   

Abstract

These studies were designed to determine whether small cytoplasmic RNAs and two different mRNAs (actin mRNA and histone H4 mRNA) were uniformly distributed among various subcellular compartments. The cytoplasm of HeLa S3 cells was fractionated into four RNA-containing compartments. The RNAs bound to the cytoskeleton were separated from those in the soluble cytoplasmic phase and each RNA fraction was further separated into those bound and those not bound to polyribosomes. The four cytoplasmic RNA fractions were analysed to determine which RNA species were present in each. The 7 S RNAs were found in all cytoplasmic fractions, as were the 5 S and 5.8 S ribosomal RNAs, while transfer RNA was found largely in the soluble fraction devoid of polysomes. On the other hand a group of prominent small cytoplasmic RNAs (scRNAs of 105-348 nucleotides) was isolated from the fraction devoid of polysomes but bound to the cytoskeleton. Actin mRNA was found only in polyribosomes bound to the cytoskeleton. This mRNA was released into the soluble phase by cytochalasin B treatment, suggesting a dependence upon actin filament integrity for cytoskeletal binding. A significant portion of several scRNAs was also released from the cytoskeleton by cytochalasin B treatment. Analysis of the spatial distribution of histone H4 mRNAs, however, revealed a more widely dispersed message. Although most (60%) of the H4 mRNA was associated with polyribosomes in the soluble phase, a significant amount was also recovered in both of the cytoskeleton bound fractions either associated or free of polyribosome interaction. Treatment with cytochalasin B suggested that only cytoskeleton bound, untranslated H4 mRNA was dependent upon the integrity of actin filaments for cytoskeletal binding.

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Year:  1986        PMID: 2431717     DOI: 10.1016/0167-4781(86)90057-6

Source DB:  PubMed          Journal:  Biochim Biophys Acta        ISSN: 0006-3002


  12 in total

1.  Influence of metallothionein-1 localization on its function.

Authors:  M Levadoux-Martin; J E Hesketh; J H Beattie; H M Wallace
Journal:  Biochem J       Date:  2001-04-15       Impact factor: 3.857

2.  Distinct RNP complexes of shuttling hnRNP proteins with pre-mRNA and mRNA: candidate intermediates in formation and export of mRNA.

Authors:  S Mili; H J Shu; Y Zhao; S Piñol-Roma
Journal:  Mol Cell Biol       Date:  2001-11       Impact factor: 4.272

3.  "In situ" translation: use of the cytoskeletal framework to direct cell-free protein synthesis.

Authors:  D Biegel; J S Pachter
Journal:  In Vitro Cell Dev Biol       Date:  1991-01

4.  c-myc mRNA in cytoskeletal-bound polysomes in fibroblasts.

Authors:  J E Hesketh; G P Campbell; P F Whitelaw
Journal:  Biochem J       Date:  1991-03-01       Impact factor: 3.857

5.  The characterization of free, cytoskeletal and membrane-bound polysomes in Krebs II ascites and 3T3 cells.

Authors:  A Vedeler; I F Pryme; J E Hesketh
Journal:  Mol Cell Biochem       Date:  1991-02-02       Impact factor: 3.396

Review 6.  Interaction between mRNA, ribosomes and the cytoskeleton.

Authors:  J E Hesketh; I F Pryme
Journal:  Biochem J       Date:  1991-07-01       Impact factor: 3.857

7.  The mRNAs for cyclin A, c-myc and ribosomal proteins L4 and S6 are associated with cytoskeletal-bound polysomes in HepG2 cells.

Authors:  R Hovland; G Campbell; I Pryme; J Hesketh
Journal:  Biochem J       Date:  1995-08-15       Impact factor: 3.857

8.  A general RNA-binding protein complex that includes the cytoskeleton-associated protein MAP 1A.

Authors:  C DeFranco; M E Chicurel; H Potter
Journal:  Mol Biol Cell       Date:  1998-07       Impact factor: 4.138

9.  Immunological and chemical characterization of hamster brain polyribosomes-cytomatrix complexes.

Authors:  I Bouhtiauy; Y Choukri; C Turpin; D Gauthier
Journal:  Neurochem Res       Date:  1989-07       Impact factor: 3.996

Review 10.  Translation and the cytoskeleton: a mechanism for targeted protein synthesis.

Authors:  J Hesketh
Journal:  Mol Biol Rep       Date:  1994-05       Impact factor: 2.316

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