The Myc/Max/Mad Transcription Factor Network

Intense study of the enigmatic myc proto-oncogene over the last 20 years has broadened our view of its functions and led to insights into transcriptional regulation as well as cancer etiology, cell proliferation, apoptosis, and organismal development

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Editors R.W. Compans, Atlanta/Georgia M.D. Cooper, Birmingham/Alabama T. Honjo, Kyoto · H. Koprowski, Philadelphia/Pennsylvania F. Melchers, Basel · M.B.A. Oldstone, La Jolla/California S. Olsnes, Oslo · M. Potter, Bethesda/Maryland P.K. Vogt, La Jolla/California · H. Wagner, Munich

R.N. Eisenman (Ed.)

The Myc/Max/Mad Transcription Factor Network With 28 Figures and 3 Tables

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Robert N. Eisenman, Prof. Dr., Ph.D. Division of Basic Sciences Fred Hutchinson Cancer Research Center P.O. Box 19024 Seattle, Washington 98108-1024 USA e-mail: [email protected] Cover Illustration: The cover figure depicts a Myc-Max protein heterodimer interacting with its CACGTG binding site in DNA, superimposed over an image of DAPI-stained cell nuclei. The large cell nuclei are located within a Drosophila larval salivary gland ectopically expressing Drosophila Myc (dMyc) while the small nuclei are from fat body cells lacking ectopic dMyc (from Pierce SB, Yost C, Britton JS, Loo LW, Flynn EM, Edgar BA, Eisenman RN (2004) dMyc is required for larval growth and endoreplication in Drosophila. Development 131: 2317-2327). See chapter by Nair and Burley, within, for review of structural studies on Myc-Max dimers.

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Preface

Scientists often look askance at their colleagues whose research appears too strongly focused on a single gene or gene product. We are supposed to be inter