» Articles » PMID: 7517985

Suppression of Mitochondrial MRNA Levels and Mitochondrial Function in Cells Responding to the Anticellular Action of Interferon

Overview
Publisher Mary Ann Liebert
Date 1994 Feb 1
PMID 7517985
Citations 7
Authors
Affiliations
Soon will be listed here.
Abstract

A lambda cDNA library prepared from polyadenylated RNA isolated from Daudi cells was differentially screened to isolate cDNAs that recognize mRNA whose levels are reduced following interferon (IFN) treatment. Southern blot and DNA sequence analysis of 20 cDNA clones that were isolated revealed that they represented mitochondrially encoded mRNAs for the following proteins: cytochrome c oxidase subunits II and III, ATPase 6, cytochrome b, and subunit 1 of the NADH dehydrogenase. Northern blot analysis employing these cDNAs and oligonucleotides generated to the remaining mitochondrially encoded mRNAs demonstrated that IFN-alpha treatment of Daudi cells mediates a time-dependent suppression of the level of all of the mitochondrially encoded mRNAs. Study of this IFN-mediated effect reveals that: (i) the suppression of the level of these mRNAs is dependent on protein synthesis, (ii) it can be observed to occur prior to any detectable effect on thymidine incorporation, (iii) the degree of suppression correlates with the sensitivity of the cells to the anticellular action of IFN, and (iv) the suppression of the level of these RNAs appears to result from an effect on the level of transcription rather than on the stability of these mRNAs. A study of the level of cellular respiration in IFN-treated Daudi cells reveals a clear suppression 3 h following IFN treatment.

Citing Articles

IFN-γ restores the impaired function of RNase L and induces mitochondria-mediated apoptosis in lung cancer.

Yin H, Jiang Z, Wang S, Zhang P Cell Death Dis. 2019; 10(9):642.

PMID: 31501431 PMC: 6733796. DOI: 10.1038/s41419-019-1902-9.


Human Cytomegalovirus Infection Upregulates the Mitochondrial Transcription and Translation Machineries.

Karniely S, Weekes M, Antrobus R, Rorbach J, van Haute L, Umrania Y mBio. 2016; 7(2):e00029.

PMID: 27025248 PMC: 4807356. DOI: 10.1128/mBio.00029-16.


Multi-tasking: nuclear transcription factors with novel roles in the mitochondria.

Szczepanek K, Lesnefsky E, Larner A Trends Cell Biol. 2012; 22(8):429-37.

PMID: 22705015 PMC: 3516366. DOI: 10.1016/j.tcb.2012.05.001.


Diverse functions of RNase L and implications in pathology.

Bisbal C, Silverman R Biochimie. 2007; 89(6-7):789-98.

PMID: 17400356 PMC: 2706398. DOI: 10.1016/j.biochi.2007.02.006.


Tyk2 tyrosine kinase expression is required for the maintenance of mitochondrial respiration in primary pro-B lymphocytes.

Potla R, Koeck T, Wegrzyn J, Cherukuri S, Shimoda K, Baker D Mol Cell Biol. 2006; 26(22):8562-71.

PMID: 16982690 PMC: 1636766. DOI: 10.1128/MCB.00497-06.