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PMID: 3683391 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Transcriptionally inactive oocyte-type 5S RNA genes of Xenopus laevis are complexed with TFIIIA in vitro.

Molecular and cellular biology ·Vol. 7 ·No. 10 ·1987-10-00 ·Pages 3503-10

Peck LJ, Millstein L, Eversole-Cire P, Gottesfeld JM, Varshavsky A

Abstract

An extract from whole oocytes of Xenopus laevis was shown to transcribe somatic-type 5S RNA genes approximately 100-fold more efficiently than oocyte-type 5S RNA genes. This preference was at least 10-fold greater than the preference seen upon microinjection of 5S RNA genes into oocyte nuclei or upon in vitro transcription in an oocyte nuclear extract. The approximately 100-fold transcriptional bias in favor of the somatic-type 5S RNA genes observed in vitro in the whole oocyte extract was similar to the transcriptional bias observed in developing Xenopus embryos. We also showed that in the whole oocyte extract, a promoter-binding protein required for 5S RNA gene transcription, TFIIIA, was bound both to the actively transcribed somatic-type 5S RNA gene and to the largely inactive oocyte-type 5S RNA genes. These findings suggest that the mechanism for the differential expression of 5S RNA genes during Xenopus development does not involve differential binding of TFIIIA to 5S RNA genes.

MeSH Terms
Animals Cloning, Molecular DNA, Ribosomal/metabolism DNA-Binding Proteins/metabolism Deoxyribonuclease I Gene Expression Regulation Genes Oocytes/physiology Plasmids RNA, Ribosomal/genetics RNA, Ribosomal, 5S/genetics Transcription Factors/metabolism Transcription, Genetic Xenopus laevis/genetics
Chemicals
DNA, Ribosomal DNA-Binding Proteins RNA, Ribosomal RNA, Ribosomal, 5S Transcription Factors Deoxyribonuclease I
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Peck L J
Department of Biology, Massachusetts Institute of Technology, Cambridge 02139.
Millstein L
Eversole-Cire P
Gottesfeld J M
Varshavsky A
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34 references, click to expand
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Article Info
Journal
Molecular and cellular biology
Abbr.
Mol Cell Biol
ISSN
0270-7306
Published
1987-10-00
Pages
3503-10
Language
English
Region
United States
NLM ID
8109087
PMCID
PMC368002
Subset
IM
Grants
NCI NIH HHS · CA43309 · United States
NIGMS NIH HHS · GM26453 · United States
NIGMS NIH HHS · GM33401 · United States
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