Literature DB >> 14167

The in vivo effect of dimethyl sulphoxide (DMSO) on protein synthesis and the polyribosome profile in Paramecium.

A H Reisner, C Bucholtz.   

Abstract

When Paramecium tetraurelia in log phase growth is treated with 4% dimethyl sulphoxide (DMSO) for five minutes the amount of polyribosomes is reduced 3- to 4-fold while there is a corresponding increase in 80s ribosomal material. Reducing the concentration of DMSO to 1% allows immediate reversal of the condition. Paramecium polyribosomes subjected to 4% DMSO either in whole cell homogenates or during purification through sucrose density gradients appear unaffected while cycloheximide at concentrations up to 100 mug/ml did not prevent DMSO from exerting its effect in vivo. Analyses of 14C amino acid incorporation experiments indicated a strict correspondence between the effect of DMSO on polyribosomes and overall protein synthesis. The reduction of acid precipitable radioactivity in the polyribosomal region after DMSO treatment was associated with a corresponding increase in radioactivity in the 80s region. There was no comparable increase in the acid precipitable radioactivity in the soluble fraction. The overall results of the study suggest that DMSO acts on polyribosommes indirectly through some unknown primary reaction with cell constitutents, and that the mode of action is such as to cause the release of ribosomes from messenger RNA (mRNA) rather than to prevent initiation of the ribosome-mRNA complex. Our data suggest that the effect may be selective. Finally, it is of interest that high concentrations of DMSO (above 8%) appear to have the opposite effect of lower concentrations of DMSO, i.e., they appear to "freeze" the ribosomes to mRNA.

Entities:  

Mesh:

Substances:

Year:  1977        PMID: 14167     DOI: 10.1002/jcp.1040900204

Source DB:  PubMed          Journal:  J Cell Physiol        ISSN: 0021-9541            Impact factor:   6.384


  2 in total

1.  Estrogen receptor alpha increases basal and cigarette smoke extract-induced expression of CYP1A1 and CYP1B1, but not GSTP1, in normal human bronchial epithelial cells.

Authors:  W Han; B T Pentecost; R L Pietropaolo; M J Fasco; S D Spivack
Journal:  Mol Carcinog       Date:  2005-11       Impact factor: 4.784

2.  Enhancing transient protein expression in HEK-293 cells by briefly exposing the culture to DMSO.

Authors:  Janet Lynch; JiWoo Chung; Zhen Huang; Vincen Pierce; Noah S Saunders; Li Niu
Journal:  J Neurosci Methods       Date:  2020-12-24       Impact factor: 2.987

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.