Note to users. If you're seeing this message, it means that your browser cannot find this page's style/presentation instructions -- or possibly that you are using a browser that does not support current Web standards. Find out more about why this message is appearing, and what you can do to make your experience of our site the best it can be.
Invitrogen

Site Tools

  • AAAS
  • Subscribe
  • Feedback

Site Search

Search Advanced

Science 1 February 2008:
Vol. 319. no. 5863, pp. 620 - 624
DOI: 10.1126/science.1149200

Reports

Cancer Proliferation Gene Discovery Through Functional Genomics

Michael R. Schlabach,1* Ji Luo,1* Nicole L. Solimini,1* Guang Hu,1* Qikai Xu,1 Mamie Z. Li,1 Zhenming Zhao,1 Agata Smogorzewska,1,2 Mathew E. Sowa,3 Xiaolu L. Ang,3 Thomas F. Westbrook,1 Anthony C. Liang,1 Kenneth Chang,4 Jennifer A. Hackett,1 J. Wade Harper,3 Gregory J. Hannon,4 Stephen J. Elledge1{dagger}

Retroviral short hairpin RNA (shRNA)–mediated genetic screens in mammalian cells are powerful tools for discovering loss-of-function phenotypes. We describe a highly parallel multiplex methodology for screening large pools of shRNAs using half-hairpin barcodes for microarray deconvolution. We carried out dropout screens for shRNAs that affect cell proliferation and viability in cancer cells and normal cells. We identified many shRNAs to be antiproliferative that target core cellular processes, such as the cell cycle and protein translation, in all cells examined. Moreover, we identified genes that are selectively required for proliferation and survival in different cell lines. Our platform enables rapid and cost-effective genome-wide screens to identify cancer proliferation and survival genes for target discovery. Such efforts are complementary to the Cancer Genome Atlas and provide an alternative functional view of cancer cells.

1 Howard Hughes Medical Institute and Department of Genetics, Center for Genetics and Genomics, Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02115, USA.
2 Department of Pathology, Massachusetts General Hospital (MGH), Boston, MA 02114, USA.
3 Department of Pathology, Harvard Medical School, Boston, MA 02115, USA.
4 Watson School of Biological Sciences, Howard Hughes Medical Institute, Cold Spring Harbor Laboratory, 1 Bungtown Road, Cold Spring Harbor, NY 11724, USA.

* These authors contributed equally to this work.

{dagger} To whom correspondence should be addressed. E-mail: selledge{at}genetics.med.harvard.edu

Read the Full Text



THIS ARTICLE HAS BEEN CITED BY OTHER ARTICLES:
Profiling Essential Genes in Human Mammary Cells by Multiplex RNAi Screening.
J. M. Silva, K. Marran, J. S. Parker, J. Silva, M. Golding, M. R. Schlabach, S. J. Elledge, G. J. Hannon, and K. Chang (2008)
Science 319, 617-620
   Abstract »    Full Text »    PDF »



ADVERTISEMENT
Click Me!

ADVERTISEMENT
Click Me!

To Advertise     Find Products


Science. ISSN 0036-8075 (print), 1095-9203 (online)