Conservation of the sequence and temporal expression of let-7 heterochronic regulatory RNA
By A. Pasquinelli, B. Reinhart, Frank J. Slack, M. Martindale, M. Kuroda, Betsy Maller, D. Hayward, E. Ball, B. Degnan, P. Müller and 9 more. Nature, 2000
2,685 citations recorded by the source corpus.
Subfields: Aging, Molecular Biology
View Paper: https://www.semanticscholar.org/paper/aaef86016a0a2e9ad44803875035b81c34d8dff4
How researchers see this paper
The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.
In Aging
- David P. Bartel
- Thomas Tuschl
- Phillip D. Zamore
- V. Narry Kim
- E. Miska
- V. Ambros
- Eric C. Lai
- M. Jones-Rhoades
In Molecular Biology
- David P. Bartel
- Phillip D. Zamore
- Nikolaus Rajewsky
- Scott M. Hammond
- V. Narry Kim
- Thomas Tuschl
- Frank J. Slack
- Carlo Maria Croce
Citations in the corpus
- bantam encodes a developmentally regulated microRNA that controls cell proliferation and regulates the proapoptotic gene hid in Drosophila. (2003, background): “Hedgehog and Dpp signaling (e.g., Pasquinelli et al., 2000).”
- Non–coding RNA genes and the modern RNA world (2001, background): “Surprisingly,Amy Pasquinelli et al.(87) showed that let-7 was almost 100% conserved and expressed as a small 21nucleotide RNA in all bilaterally symmetrical animals that were tested, including human, mouse, chicken, polychaete worms and flies, but not in cnidarians (jellyfish) or poriferans (sponges”
- Lin28 mediates the terminal uridylation of let-7 precursor MicroRNA. (2008, background): “…ª2008 Elsevier In let-7 RNA, highly conserved in bilaterian animals, controls developmental timing (Grosshans et al., 2005; Meneely and Herman, 1979; Pasquinelli et al., 2000; Reinhart et al., 2000). let-7 also functions as a tumor suppressor by targeting RAS, HMGA2, and c-Myc (Johnson et al.,…”
- Noncoding RNA gene detection using comparative sequence analysis (2001, background): “Recent discoveries have included RNAs involved in dosage compensation and imprinting [5], numerous small nucleolar RNAs involved in RNA modification and processing [6–8], and small riboregulatory RNAs controlling translation and/or stability of target mRNAs [9,10].”
- Gene silencing in plants using artificial microRNAs and other small RNAs. (2008, background): “elegans, let-7, and the discovery of let-7 homologs in the genomes of many other animals including humans (Pasquinelli et al., 2000; Reinhart et al., 2000).”
- A biochemical framework for RNA silencing in plants. (2003, background): “miRNAs are produced by Dicer cleavage of stem–loop precursor RNA transcripts (pre-miRNAs); the miRNA can reside on either the 5 or 3 side of the doublestranded stem (Lee et al. 1993; Pasquinelli et al. 2000; Lagos-Quintana et al. 2001; Lau et al. 2001; Lee and Ambros 2001).”
- MicroRNAs in Common Human Diseases (2012, background): “demonstrated that the let-7 sequence was highly conserved across the evolutionary spectrum [5], biologists started to realize that this tiny RNA molecule may have a big role to play in humans as well [6].”
- The Genetic Signatures of Noncoding RNAs (2009, background): “elegans, not in other organisms, despite the former being not only highly conserved in sequence and expression pattern throughout metazoan evolution [139], but also fundamental to normal and abnormal developmental processes [140– 142], as are many other miRNAs [143].”
- Computational and experimental identification of C. elegans microRNAs. (2003, methodology): “The best described targets comprise two imperfect duplexes between let-7 and the 3′ UTR of lin-41, and seven imperfect duplexes between lin-4 and the 3′-UTR of lin-14 (Lee et al., 1993; Reinhart et al., 2000; Wightman et al., 1993; Slack et al., 2000; Pasquinelli et al., 2000).”