David Bartel Explained

David P. Bartel
Nationality:American
Fields:Biochemistry, Molecular Biology
Workplaces:Whitehead Institute, Massachusetts Institute of Technology
Alma Mater:Goshen College, Harvard University
Thesis Title:RNA recognition and catalysis : I. New ribozymes from random sequences ; II. The HIV rev-RRE interaction
Thesis Year:1993
Doctoral Advisor:Jack Szostak
Known For:MicroRNAs

David P. Bartel is an American molecular biologist best known for his work on microRNAs. Bartel is a Professor of Biology at the Massachusetts Institute of Technology, Member of the Whitehead Institute, and investigator of the Howard Hughes Medical Institute (HHMI).

Biography

Bartel earned his B.A. degree in biology from Goshen College in 1982 and his Ph.D. degree in virology from Harvard University in 1993, under the mentorship of Jack W. Szostak.[1]

While in the Szostak lab, Bartel isolated the first ribozymes directly from random sequence, using in vitro evolution (among these, the Class I ligase).[2] After he became independent at the Whitehead Institute, he further evolved this ribozyme to function as a RNA-dependent RNA polymerase to extend primers on external RNA templates, bolstering the "RNA world" theory.[3] [4]

Bartel later shifted his research focus towards microRNA biology and in particular on understanding their regulatory functions.[5] MicroRNAs are short pieces of RNA, about 22 nucleotides long, that dampen gene expression through the silencing of messenger RNAs (mRNAs). His lab was one of three that found that animals have many of these small regulatory RNAs,[6] [7] [8] and he was the first to describe microRNAs in plants.[9] [10] Through his work with microRNAs, he developed a methodology that predicts their regulatory targets and created the web-based tool TargetScan, which makes these predictions available to the research community.[11] [12] [13] [14] [15] His research has also shown that most human mRNAs are regulated by microRNAs and that microRNAs predominantly act to decrease the levels of their mRNA targets.[16]

Bartel also discovered several other types of regulatory RNAs, including heterochromatic siRNAs, which silence DNA instead of RNA.[17] In addition, Bartel is investigating the roles of long non-coding RNAs (lncRNAs) and how the untranslated regions and tails of mRNAs recruit and mediate regulatory phenomena.[5]

Bartel is a founder and a scientific advisor of Alnylam Pharmaceuticals, a company started in 2002 to advance “RNAi (RNA interference) therapeutics as a new class of innovative medicines”.[18]

In 2006, Bartel was placed second by Thomson Reuters in a 'citations' ranking in the field of Molecular Biology/Genetics.He has received several awards and was elected to the National Academy of Sciences in 2011.[19]

External links

Notes and References

  1. News: David P. Bartel '82. 8 March 2014. Goshen Bulletin. 2007.
  2. Science. 1993 Sep 10;261(5127):1411-8. "Isolation of new ribozymes from a large pool of random sequences." Bartel DP, Szostak JW.
  3. Trends Cell Biol. 1999 Dec;9(12):M9-M13. "Constructing an RNA world." Bartel DP, Unrau PJ.
  4. Johnston. WK. Unrau. PJ. Lawrence. MS. Glasner. ME. Bartel. DP. RNA-catalyzed RNA polymerization: accurate and general RNA-templated primer extension.. Science. 18 May 2001. 292. 5520. 1319–25. 11358999. 10.1126/science.1060786. 2001Sci...292.1319J. 10.1.1.70.5439. 14174984.
  5. Web site: David Bartel. HHMI. 7 October 2016.
  6. "Science". 2001 Oct 26;294(5543):853-8. "Identification of novel genes coding for small expressed RNAs." Lagos-Quintana M1, Rauhut R, Lendeckel W, Tuschl T.
  7. "Science". 2001 Oct 26;294(5543):858-62. "An abundant class of tiny RNAs with probable regulatory roles in Caenorhabditis elegans." Lau NC1, Lim LP, Weinstein EG, Bartel DP.
  8. "Science". 2001 Oct 26;294(5543):862-4. "An extensive class of small RNAs in Caenorhabditis elegans. Lee RC1, Ambros V.
  9. "Genes Dev." 2002 Jul 1;16(13):1616-26. "MicroRNAs in plants." Reinhart BJ1, Weinstein EG, Rhoades MW, Bartel B, Bartel DP.
  10. "Cell". 2002 Aug 23;110(4):513-20."Prediction of plant microRNA targets." Rhoades MW1, Reinhart BJ, Lim LP, Burge CB, Bartel B, Bartel DP.
  11. "Cell". 2005 Jan 14;120(1):15-20. "Conserved seed pairing, often flanked by adenosines, indicates that thousands of human genes are microRNA targets." Lewis BP, Burge CB, Bartel DP.
  12. "Mol Cell". 2007 Jul 6;27(1):91-105. "MicroRNA targeting specificity in mammals: determinants beyond seed pairing." Grimson A1, Farh KK, Johnston WK, Garrett-Engele P, Lim LP, Bartel DP.
  13. "Genome Res." 2009 Jan;19(1):92-105. "Most mammalian mRNAs are conserved targets of microRNAs." Friedman RC1, Farh KK, Burge CB, Bartel DP.
  14. Predicting effective microRNA target sites in mammalian mRNAs . eLife . 2015-08-12 . 2050-084X . 4532895 . 26267216 . e05005 . 4 . 10.7554/eLife.05005 . en . Vikram . Agarwal . George W. . Bell . Jin-Wu . Nam . David P. . Bartel . free .
  15. Agarwal . V . Subtelny . AO . Thiru . P . Ulitsky . I . Bartel . DP . Predicting microRNA targeting efficacy in Drosophila. . Genome Biology . 4 October 2018 . 19 . 1 . 152 . 10.1186/s13059-018-1504-3 . 30286781. 6172730 . free .
  16. Guo. H. Ingolia. NT. Weissman. JS. Bartel. DP. Mammalian microRNAs predominantly act to decrease target mRNA levels.. Nature. 12 August 2010. 466. 7308. 835–40. 20703300. 10.1038/nature09267. 2990499. 2010Natur.466..835G.
  17. Reinhart. BJ. Bartel. DP. 42288846. Small RNAs correspond to centromere heterochromatic repeats.. Science. 13 September 2002. 297. 5588. 1831. 12193644. 10.1126/science.1077183.
  18. Web site: Scientific Advisory Board. Alnylam.com. 5 October 2016.
  19. Web site: Whitehead Member David Bartel elected to National Academy of Sciences . 25 January 2015.