In vivo CRISPR screening identifies SAGA complex members as key regulators of hematopoiesis

作者：Michael S. Haney, Archana Shankar, Leonid Olender, Ian Hsu, Masashi Miyauchi, Róbert Pálovics, Grace A. Meaker, Satoshi Kaito, Ola Rizq, Hwei Minn Khoo, Yavor Bozhilov, Kyomi J. Igarashi, Joydeep Bhadury, Christy Munson, Paul Mack, Tze-Kai Tan, Jan Rehwinkel, Atushi Iwama, Tony Wyss‐Coray, Hiromitsu Nakauchi, Adam C. Wilkinson · 发表于：bioRxiv (Cold Spring Harbor Laboratory) · 年份：2022 · DOI：10.1101/2022.07.22.501030 · 被引用次数：7 · 研究领域：Cytomegalovirus and herpesvirus research、Immune Cell Function and Interaction、Virus-based gene therapy research

Abstract The biological mechanisms that sustain the vast blood production required for healthy life remain incompletely understood. To search for novel regulators of hematopoiesis, we performed genome-wide in vivo hematopoietic stem cell (HSC)-based CRISPR knockout screens for regulators of hematopoiesis. We discovered SAGA complex members, including Tada2b and Taf5l , as key regulators of hematopoiesis. Loss of Tada2b or Taf5l strongly inhibited hematopoiesis in vivo , led to a buildup of immature hematopoietic cells in the bone marrow, and was associated with upregulation of interferon pathway genes. Loss of these factors also enhanced the cell outgrowth and the interferon pathway in an in vivo human myelodysplastic syndrome model, suggesting that loss of SAGA complex activity could contribute to hematological disease progression. In summary, this study has identified the SAGA complex as an important regulator of hematopoiesis.