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PMID: 11081512 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Conservation of the sequence and temporal expression of let-7 heterochronic regulatory RNA.

Nature ·Vol. 408 ·No. 6808 ·2000-11-02 ·Pages 86-9

Pasquinelli AE, Reinhart BJ, Slack F, Martindale MQ, Kuroda MI, Maller B, Hayward DC, Ball EE, Degnan B, Müller P, Spring J, Srinivasan A, Fishman M, Finnerty J, Corbo J, Levine M, Leahy P, Davidson E, Ruvkun G

Abstract

Two small RNAs regulate the timing of Caenorhabditis elegans development. Transition from the first to the second larval stage fates requires the 22-nucleotide lin-4 RNA, and transition from late larval to adult cell fates requires the 21-nucleotide let-7 RNA. The lin-4 and let-7 RNA genes are not homologous to each other, but are each complementary to sequences in the 3' untranslated regions of a set of protein-coding target genes that are normally negatively regulated by the RNAs. Here we have detected let-7 RNAs of approximately 21 nucleotides in samples from a wide range of animal species, including vertebrate, ascidian, hemichordate, mollusc, annelid and arthropod, but not in RNAs from several cnidarian and poriferan species, Saccharomyces cerevisiae, Escherichia coli or Arabidopsis. We did not detect lin-4 RNA in these species. We found that let-7 temporal regulation is also conserved: let-7 RNA expression is first detected at late larval stages in C. elegans and Drosophila, at 48 hours after fertilization in zebrafish, and in adult stages of annelids and molluscs. The let-7 regulatory RNA may control late temporal transitions during development across animal phylogeny.

Keywords
Non-programmatic
MeSH Terms
Adult Animals Base Sequence Caenorhabditis elegans/genetics Conserved Sequence Drosophila melanogaster Gene Expression Regulation, Developmental Humans Molecular Sequence Data Phylogeny RNA/chemistry,genetics RNA, Helminth Species Specificity
Chemicals
RNA, Helminth RNA
Authors & Affiliations
19 authors, click to expand affiliations / ORCID
Pasquinelli A E
Department of Molecular Biology, Massachusetts General Hospital, Harvard Medical School, Boston 02114, USA.
Reinhart B J
Slack F
Martindale M Q
Kuroda M I
Maller B
Hayward D C
Ball E E
Degnan B
Müller P
Spring J
Srinivasan A
Fishman M
Finnerty J
Corbo J
Levine M
Leahy P
Davidson E
Ruvkun G
Article Info
Journal
Nature
Abbr.
Nature
ISSN
0028-0836
Published
2000-11-02
Pages
86-9
Language
English
Region
England
NLM ID
0410462
Subset
IM
Grants
NIAMS NIH HHS · P30 AR046032 · United States
NIGMS NIH HHS · R01 GM045744 · United States
Corrections
CommentIn
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