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PMID: 9247343 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Nanos and pumilio establish embryonic polarity in Drosophila by promoting posterior deadenylation of hunchback mRNA.

Development (Cambridge, England) ·Vol. 124 ·No. 15 ·1997-08-00 ·Pages 3015-23

Wreden C, Verrotti AC, Schisa JA, Lieberfarb ME, Strickland S

Abstract

Nanos protein promotes abdominal structures in Drosophila embryos by repressing the translation of maternal hunchback mRNA in the posterior. To study the mechanism of nanos-mediated translational repression, we first examined the mechanism by which maternal hunchback mRNA is translationally activated. In the absence of nanos activity, the poly(A) tail of hunchback mRNA is elongated concomitant with its translation, suggesting that cytoplasmic polyadenylation directs activation. However, in the presence of nanos the length of the hunchback mRNA poly(A) tail is reduced. To determine if nanos activity represses translation by altering the polyadenylation state of hunchback mRNA, we injected various in vitro transcribed RNAs into Drosophila embryos and determined changes in polyadenylation. Nanos activity reduced the polyadenylation status of injected hunchback RNAs by accelerating their deadenylation. Pumilio activity, which is necessary to repress the translation of hunchback, is also needed to alter polyadenylation. An examination of translation indicates a strong correlation between poly(A) shortening and suppression of translation. These data indicate that nanos and pumilio determine posterior morphology by promoting the deadenylation of maternal hunchback mRNA, thereby repressing its translation.

MeSH Terms
Animals Body Patterning/genetics DNA-Binding Proteins/genetics Drosophila/embryology,genetics Drosophila Proteins Gene Expression Regulation, Developmental/physiology Homeodomain Proteins/genetics Insect Proteins/genetics,physiology Models, Genetic Protein Biosynthesis/physiology RNA, Messenger/metabolism RNA-Binding Proteins Trans-Activators/genetics Transcription Factors/genetics
Chemicals
DNA-Binding Proteins Drosophila Proteins Homeodomain Proteins Insect Proteins RNA, Messenger RNA-Binding Proteins Trans-Activators Transcription Factors bcd protein, Drosophila hb protein, Drosophila pum protein, Drosophila nos protein, Drosophila
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Wreden C
Department of Pharmacology, University Medical Center at Stony Brook, NY 11794-8651, USA.
Verrotti A C
Schisa J A
Lieberfarb M E
Strickland S
Article Info
Journal
Development (Cambridge, England)
Abbr.
Development
ISSN
0950-1991
Published
1997-08-00
Pages
3015-23
Language
English
Region
England
NLM ID
8701744
Subset
IM
Grants
NIGMS NIH HHS · GM51584 · United States
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