Your Waterstones card is changing, introducing...
TELL ME MORE
miRNA Regulation of the Translational Machinery - Progress in Molecular and Subcellular Biology 50 (Paperback)
  • miRNA Regulation of the Translational Machinery - Progress in Molecular and Subcellular Biology 50 (Paperback)
zoom

miRNA Regulation of the Translational Machinery - Progress in Molecular and Subcellular Biology 50 (Paperback)

(editor)
£119.99
Paperback 115 Pages / Published: 14/03/2012
  • We can order this

Usually despatched within 3 weeks

  • This item has been added to your basket
An odd and unexpected finding was reported by the laboratory of Richard Jorgensen in 1990: expression of extra copies of the gene encoding chalone synthase in petunias turned off the endogenous chalone synthase gene. An observation that appeared totally unrelated was made by the laboratory of Victor Ambrose in 1993: a gene in Caenorhabditis elegans, lin-4, controlled the timing of larval development but did not encode a protein. Rather, it expressed two small RNAs that were complementary to the 3'-untranslated region of the lin-14 gene in a region that had previously been shown to repress expression of the LIN-14 protein. From another quarter, David Baulcombe's laboratory showed in 1997 that plant viruses could induce sequen- specific gene silencing. Then in a landmark paper, Andrew Fire and Craig Mello showed in 1998 that double-stranded RNA (dsRNA) triggers a gene-silencing mechanism that they dubbed RNA interference (RNAi), for which discovery they were awarded the Nobel Prize in Physiology or Medicine in 2006. These diverse findings have triggered an explosion of research around the world in both plants and animals to discover the mechanisms and broader ramifications of RNAi. We now know that there are both exogenous pathways involving formation of siRNA when dsRNA is introduced and endogenous pathways involving miRNA, piwiRNA, and rasiRNAs. All pathways culminate in formation of an RNA-induced silencing complex (RISC) containing a member of the Argonaute protein family bound to a 22-nt RNA strand that interacts with a target mRNA or gene through Watson-Crick base pairing.

Publisher: Springer-Verlag Berlin and Heidelberg GmbH & Co. KG
ISBN: 9783642261404
Number of pages: 115
Weight: 207 g
Dimensions: 235 x 155 x 7 mm
Edition: 2010 ed.

You may also be interested in...

Biochemistry For Dummies
Added to basket
Introduction to Bioinformatics
Added to basket
The Chemistry of Life
Added to basket
Immunology
Added to basket
£42.99
Paperback
The Cell: A Very Short Introduction
Added to basket
Bioluminescence
Added to basket
£35.95
Hardback
Hormones: A Very Short Introduction
Added to basket
Exploring Proteins
Added to basket
Schaum's Outline of Immunology
Added to basket
General, Organic, and Biochemistry
Added to basket
Medical Biochemistry at a Glance
Added to basket
Chemistry for the Biosciences
Added to basket
The Machinery of Life
Added to basket
Infection & Immunity
Added to basket

Reviews

Please sign in to write a review

Your review has been submitted successfully.