A genome-wide genetic screen uncovers determinants of human pigmentation

Author:

Bajpai Vivek K.123ORCID,Swigut Tomek1ORCID,Mohammed Jaaved12ORCID,Naqvi Sahin124ORCID,Arreola Martin2ORCID,Tycko Josh4ORCID,Kim Tayne C.12ORCID,Pritchard Jonathan K.45ORCID,Bassik Michael C.467ORCID,Wysocka Joanna1289ORCID

Affiliation:

1. Department of Chemical and Systems Biology, Stanford University School of Medicine, Stanford, CA 94305, USA.

2. Institute for Stem Cell Biology and Regenerative Medicine, Stanford University School of Medicine, Stanford, CA 94305, USA.

3. School of Chemical, Biological, and Materials Engineering, The University of Oklahoma, Norman, OK 73019, USA.

4. Department of Genetics, Stanford University, Stanford, CA 94305, USA.

5. Department of Biology, Stanford University, Stanford, CA 94305, USA.

6. Chemistry, Engineering, and Medicine for Human Health (ChEM-H), Stanford University, Stanford, CA 94305, USA.

7. Program in Cancer Biology, Stanford University School of Medicine, Stanford, CA 94305, USA.

8. Department of Developmental Biology, Stanford University School of Medicine, Stanford, CA 94305, USA.

9. Howard Hughes Medical Institute, Stanford University School of Medicine, Stanford, CA 94305, USA.

Abstract

Skin color, one of the most diverse human traits, is determined by the quantity, type, and distribution of melanin. In this study, we leveraged the light-scattering properties of melanin to conduct a genome-wide screen for regulators of melanogenesis. We identified 169 functionally diverse genes that converge on melanosome biogenesis, endosomal transport, and gene regulation, of which 135 represented previously unknown associations with pigmentation. In agreement with their melanin-promoting function, the majority of screen hits were up-regulated in melanocytes from darkly pigmented individuals. We further unraveled functions of KLF6 as a transcription factor that regulates melanosome maturation and pigmentation in vivo, and of the endosomal trafficking protein COMMD3 in modulating melanosomal pH. Our study reveals a plethora of melanin-promoting genes, with broad implications for human variation, cell biology, and medicine.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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