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History
- February 19, 2020.
Copyright
The copyright holder for this preprint is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. All rights reserved. No reuse allowed without permission.
Author Information
- Sara H. Weitz1,
- Jen Quick-Cleveland2,8,
- Jose P. Jacob2,
- Ian Barr2,9,
- Rachel Senturia2,
- Kikuye Koyano3,
- Xinshu Xiao3,4,7,
- Shimon Weiss5,6,7 and
- Feng Guo2,7,*
- 1Interdepartmental Program in Molecular, Cellular, and Integrative Physiology, University of California, Los Angeles, California, 90095
- 2Department of Biological Chemistry, David Geffen School of Medicine, University of California, Los Angeles, California, 90095
- 3Bioinformatics Interdepartmental Program, University of California, Los Angeles, California, 90095
- 4Department of Integrative Biology and Physiology, University of California, Los Angeles, California, 90095
- 5Department of Chemistry and Biochemistry, University of California, Los Angeles, California, 90095
- 6Department of Physiology, David Geffen School of Medicine, University of California, Los Angeles, California, 90095
- 7Molecular Biology Institute, University of California, Los Angeles, California, 90095
- 8Department of Molecular Cell & Developmental Biology, University of California Santa Cruz, Santa Cruz, CA 95064
- 9Dominican University of California, San Rafael, CA 94901
- ↵*To whom correspondence should be addressed: Feng Guo, Ph.D., 611 Charles E. Young Dr. East, 202 Boyer Hall, Los Angeles, CA 90095. Fax: 310-206-7286; E-mail: fguo{at}mbi.ucla.edu
Posted February 19, 2020.
Fe(III) heme sets an activation threshold for processing distinct groups of pri-miRNAs in mammalian cells
