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Literature DB >> 3783827

Translational requirement of La Crosse virus S-mRNA synthesis: in vivo studies.

Abstract

By using methods to isolate cytoplasmic RNAs which limit degradation, the effect of drugs which inhibit protein synthesis on the accumulation of La Crosse virus plus-strand S RNAs in vivo has been studied. Cycloheximide and puromycin treatment of infected cultures caused an abortive transcript of ca. 205 nucleotides (nt) to accumulate, whereas pactamycin led to the appearance of an RNA which was slightly shorter (ca. 200 nt). Both the 205- and 200-nt RNAs contained the same range of host primers at their 5' end, but their 3' ends mapped at ca. positions 175 and 165, respectively. Examination of the sequence in this region and at the mature mRNA termination site (position 886) suggests that the sequence YAAAAAT(A)GCAG is involved in transcription termination.

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Year: 1987 PMID： 3783827 PMCID： PMC255211

Source DB: PubMed Journal: J Virol ISSN： 0022-538X Impact factor: 5.103

22 in total

1. Translational requirement of La Crosse virus S-mRNA synthesis: in vitro studies.

Authors: C Bellocq; R Raju; J Patterson; D Kolakofsky
Journal: J Virol Date: 1987-01 Impact factor: 5.103

Review 2. Bunyaviridae: recent biochemical developments.

Authors: J F Obijeski; F A Murphy
Journal: J Gen Virol Date: 1977-10 Impact factor: 3.891

3. Determination of the gene sequence of poliovirus with pactamycin.

Authors: D F Summers; J V Maizel
Journal: Proc Natl Acad Sci U S A Date: 1971-11 Impact factor: 11.205

4. An efficient mRNA-dependent translation system from reticulocyte lysates.

Authors: H R Pelham; R J Jackson
Journal: Eur J Biochem Date: 1976-08-01

5. Further studies on the inhibition of cellular protein synthesis by vesicular stomatitis virus.

Authors: M C Jaye; W Godchaux; J Lucas-Lenard
Journal: Virology Date: 1982-01-15 Impact factor: 3.616

Review 6. Priming of influenza viral RNA transcription by capped heterologous RNAs.

Authors: R M Krug
Journal: Curr Top Microbiol Immunol Date: 1981 Impact factor: 4.291

7. The use of thin acrylamide gels for DNA sequencing.

Authors: F Sanger; A R Coulson
Journal: FEBS Lett Date: 1978-03-01 Impact factor: 4.124

Review 8. Attenuation in the control of expression of bacterial operons.

Authors: C Yanofsky
Journal: Nature Date: 1981-02-26 Impact factor: 49.962

9. Peptidyl-puromycin synthesis on polyribosomes from Escherichia coli.

Authors: S Pestka
Journal: Proc Natl Acad Sci U S A Date: 1972-03 Impact factor: 11.205

10. Isolation of biologically active ribonucleic acid from sources enriched in ribonuclease.

Authors: J M Chirgwin; A E Przybyla; R J MacDonald; W J Rutter
Journal: Biochemistry Date: 1979-11-27 Impact factor: 3.162

13 in total

1. RNA binding properties of bunyamwera virus nucleocapsid protein and selective binding to an element in the 5' terminus of the negative-sense S segment.

Authors: J C Osborne; R M Elliott
Journal: J Virol Date: 2000-11 Impact factor: 5.103

10. Analysis of La Crosse virus S-segment RNA and its positive-sense transcripts in persistently infected mosquito tissues.

Authors: L J Chandler; L P Wasieloski; C D Blair; B J Beaty
Journal: J Virol Date: 1996-12 Impact factor: 5.103

Translational requirement of La Crosse virus S-mRNA synthesis: in vivo studies.

1. Translational requirement of La Crosse virus S-mRNA synthesis: in vitro studies.

Review 2. Bunyaviridae: recent biochemical developments.

3. Determination of the gene sequence of poliovirus with pactamycin.

4. An efficient mRNA-dependent translation system from reticulocyte lysates.

5. Further studies on the inhibition of cellular protein synthesis by vesicular stomatitis virus.

Review 6. Priming of influenza viral RNA transcription by capped heterologous RNAs.

7. The use of thin acrylamide gels for DNA sequencing.

Review 8. Attenuation in the control of expression of bacterial operons.

9. Peptidyl-puromycin synthesis on polyribosomes from Escherichia coli.

10. Isolation of biologically active ribonucleic acid from sources enriched in ribonuclease.

1. RNA binding properties of bunyamwera virus nucleocapsid protein and selective binding to an element in the 5' terminus of the negative-sense S segment.

2. Anti-mRNAs in La Crosse bunyavirus-infected cells.

3. Bunyavirus mRNA synthesis is coupled to translation to prevent premature transcription termination.

4. Germiston virus transcriptase requires active 40S ribosomal subunits and utilizes capped cellular RNAs.

5. La Crosse virus nucleocapsid protein controls its own synthesis in mosquito cells by encapsidating its mRNA.

6. The translational requirement for complete La Crosse virus mRNA synthesis is cell-type dependent.

7. La Crosse virus infection of mammalian cells induces mRNA instability.

8. Translational requirement of La Crosse virus S-mRNA synthesis: in vitro studies.

9. Translational requirement for La Crosse virus S-mRNA synthesis: a possible mechanism.

10. Analysis of La Crosse virus S-segment RNA and its positive-sense transcripts in persistently infected mosquito tissues.