4.7 Review

A genome editing primer for the hematologist

Journal

BLOOD
Volume 127, Issue 21, Pages 2525-2535

Publisher

AMER SOC HEMATOLOGY
DOI: 10.1182/blood-2016-01-678151

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Funding

  1. National Institutes of Health (NIH), National Heart, Lung, and Blood Institute [T32HL007574]
  2. NIH, National Institute of Diabetes and Digestive and Kidney Diseases [K08DK093705]
  3. Doris Duke Charitable Foundation
  4. Charles H. Hood Foundation
  5. American Society of Hematology
  6. Borough's Wellcome Fund
  7. Cooley's Anemia Foundation

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Gene editing enables the site-specific modification of the genome. These technologies have rapidly advanced such that they have entered common use in experimental hematology to investigate genetic function. In addition, genome editing is becoming increasingly plausible as a treatment modality to rectify genetic blood disorders and improve cellular therapies. Genome modification typically ensues from site-specific double-strand breaks and may result in a myriad of outcomes. Even single-strand nicks and targeted biochemical modifications that do not permanently alter the DNA sequence (epigenome editing) may be powerful instruments. In this review, we examine the various technologies, describe their advantages and shortcomings for engendering useful genetic alterations, and consider future prospects for genome editing to impact hematology.

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