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Genome-wide functional analysis of phosphatases in the pathogenic fungus Cryptococcus neoformans

  • Jae Hyung Jin
  • , Kyung Tae Lee
  • , Joohyeon Hong
  • , Dongpil Lee
  • , Eun Ha Jang
  • , Jin Young Kim
  • , Yeonseon Lee
  • , Seung Heon Lee
  • , Yee Seul So
  • , Kwang Woo Jung
  • , Dong Gi Lee
  • , Eunji Jeong
  • , Minjae Lee
  • , Yu Byeong Jang
  • , Yeseul Choi
  • , Myung Ha Lee
  • , Ji Seok Kim
  • , Seong Ryong Yu
  • , Jin Tae Choi
  • , Jae Won La
  • Haneul Choi, Sun Woo Kim, Kyung Jin Seo, Yelin Lee, Eun Jung Thak, Jaeyoung Choi, Anna F. Averette, Yong Hwan Lee, Joseph Heitman, Hyun Ah Kang, Eunji Cheong, Yong Sun Bahn*
*Corresponding author for this work
  • Yonsei University
  • Korea Atomic Energy Research Institute
  • Chung-Ang University
  • Korea Institute of Science and Technology
  • Duke University
  • Seoul National University

Research output: Contribution to journalJournal articlepeer-review

Abstract

Phosphatases, together with kinases and transcription factors, are key components in cellular signalling networks. Here, we present a systematic functional analysis of the phosphatases in Cryptococcus neoformans, a fungal pathogen that causes life-threatening fungal meningoencephalitis. We analyse 230 signature-tagged mutant strains for 114 putative phosphatases under 30 distinct in vitro growth conditions, revealing at least one function for 60 of these proteins. Large-scale virulence and infectivity assays using insect and mouse models indicate roles in pathogenicity for 31 phosphatases involved in various processes such as thermotolerance, melanin and capsule production, stress responses, O-mannosylation, or retromer function. Notably, phosphatases Xpp1, Ssu72, Siw14, and Sit4 promote blood-brain barrier adhesion and crossing by C. neoformans. Together with our previous systematic studies of transcription factors and kinases, our results provide comprehensive insight into the pathobiological signalling circuitry of C. neoformans.

Original languageEnglish
Article number4212
JournalNature Communications
Volume11
Issue number1
DOIs
StatePublished - 2020.12.1

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