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PMID: 8462102 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

In vivo evidence that transcription and splicing are coordinated by a recruiting mechanism.

Cell ·Vol. 73 ·No. 1 ·1993-04-09 ·Pages 47-59

Jiménez-García LF, Spector DL

Abstract

We describe the nuclear organization of pre-mRNA processing components in HeLa cells upon adenovirus 2 infection and their relationship to the localization of viral RNA sequences. We observe a redistribution of cellular splicing factors as well as RNA polymerase II and heterogeneous nuclear ribonucleoprotein particle proteins to sites of viral RNA transcription. Similar results were obtained in cells transiently transfected with a plasmid containing a portion of the beta-tropomyosin gene. Our findings demonstrate a very close association between RNA transcripts and transcription and pre-mRNA splicing factors, suggesting that these processes are both temporally and spatially linked in the cell nucleus. Furthermore, these data suggest a recruiting mechanism that regulates the localization of transcription and splicing factors in response to the initiation of active transcription.

MeSH Terms
Adenoviruses, Human/genetics Biological Transport Cell Nucleus/metabolism,ultrastructure HeLa Cells Humans Microscopy, Fluorescence Nuclear Proteins/metabolism RNA Precursors/metabolism RNA Splicing/physiology RNA, Viral/metabolism Ribonucleoproteins Serine-Arginine Splicing Factors Transcription, Genetic/physiology
Chemicals
Nuclear Proteins RNA Precursors RNA, Viral Ribonucleoproteins SRSF2 protein, human Serine-Arginine Splicing Factors
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Jiménez-García L F
Cold Spring Harbor Laboratory, New York 11724.
Spector D L
Article Info
Journal
Cell
Abbr.
Cell
ISSN
0092-8674
Published
1993-04-09
Pages
47-59
Language
English
Region
United States
NLM ID
0413066
Subset
IM
Grants
NIGMS NIH HHS · R01 GM042694 · United States
NCI NIH HHS · 5P30 CA45508-03 · United States
NIGMS NIH HHS · GM42694 · United States
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