Acer E. Xu

ORCID: 0009-0002-2628-3099
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About
Contact & Profiles
Research Areas
  • RNA regulation and disease
  • MicroRNA in disease regulation
  • Endoplasmic Reticulum Stress and Disease
  • Fungal and yeast genetics research
  • CRISPR and Genetic Engineering
  • RNA and protein synthesis mechanisms
  • RNA Interference and Gene Delivery
  • Wheat and Barley Genetics and Pathology
  • Cancer-related molecular mechanisms research

Massachusetts Institute of Technology
2021-2024

Whitehead Institute for Biomedical Research
2024

Howard Hughes Medical Institute
2015-2021

Yale University
2015

Herpesvirus saimiri (HVS) is an oncogenic γ-herpesvirus that produces microRNAs (miRNAs) by cotranscription of precursor miRNA (pre-miRNA) hairpins immediately downstream from viral small nuclear RNAs (snRNA). The host cell Integrator complex, which recognizes the snRNA 3′ end processing signal (3′ box), generates 5′ ends HVS pre-miRNA hairpins. Here, we identify a novel box-like sequence (miRNA box) pre-miRNAs essential for biogenesis. In vivo knockdown and rescue experiments confirmed also...

10.1101/gad.266973.115 article EN Genes & Development 2015-07-15

Aneuploid yeast cells are in a chronic state of proteotoxicity, yet do not constitutively induce the cytosolic unfolded protein response, or heat shock response (HSR) by factor 1 (Hsf1). Here, we demonstrate that an active environmental stress (ESR), hallmark aneuploidy across different models, suppresses Hsf1 induction models single-chromosome gain. Furthermore, engineered activation ESR absence was sufficient to suppress euploid subsequent while increasing thermotolerance and blocking...

10.1091/mbc.e21-03-0104 article EN Molecular Biology of the Cell 2021-06-30

Abstract In mammalian cells, the integrated stress response (ISR) triggers ATF4 translation under general conditions of cell stress. Mammalian target rapamycin (mTOR) signaling also pro-growth conditions. While transcriptomic changes these two contradictory pathways are have been studied, a full understanding all capable increasing and how regulated interact with each other remains unknown. genome-wide CRISPRi screen, we found that loss CARS is sufficient to activate independent canonical...

10.1101/2024.12.23.630120 preprint EN cc-by-nc-nd bioRxiv (Cold Spring Harbor Laboratory) 2024-12-23
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