Jared M. Schrader
Biochemistry, Genetics and Molecular Biology · Indiana University
Publications
68
Citations
1,491
Est. group size
—
Recurring co-author estimate
Active years
18
Publishing since 2009
Jared M. Schrader studies how bacteria manage the life cycle of their messenger RNA (mRNA)—the molecules that carry genetic instructions for making proteins. A major focus is on 'BR-bodies,' membraneless droplet-like structures inside bacterial cells that concentrate the machinery for breaking down RNA, and how these structures change their function and material properties under stress conditions such as cold or copper exposure. The lab combines genetics, biochemistry, and genome-wide sequencing methods across several bacterial species to understand RNA degradation, biomolecular condensates, and protein synthesis.
Publication activity has been steady to growing over the last decade, with recent years (2023–2025) consistently producing six to nine publications annually.
Generated by claude-opus-4-8 from public bibliographic data · Jul 11, 2026
- The <i>E. coli</i> DEAD box ATPase CsdA, is a NAD <sup>+</sup> capped RNA binding protein
bioRxiv (Cold Spring Harbor Laboratory) · 2026
- Stress changes the material state of a bacterial biomolecular condensate and shifts its function from mRNA decay to storage
Nature Communications · 2025
- BR-bodies facilitate adaptive responses and survival during copper stress in Caulobacter crescentus
Journal of Biological Chemistry · 2025
- BR-Bodies Facilitate Adaptive Responses and Survival During Copper Stress in <i>Caulobacter crescentus</i>
bioRxiv (Cold Spring Harbor Laboratory) · 2025
- Rif-seq reveals Caulobacter crescentus mRNA decay is globally coordinated with transcription and translation
Cell Reports · 2025
- Bacterial IF2’s N-terminal IDR drives cold-induced phase separation and promotes fitness during cold stress
bioRxiv (Cold Spring Harbor Laboratory) · 2025
- Rif-seq reveals <i>Caulobacter crescentus</i> mRNA decay is globally coordinated with transcription and translation
bioRxiv (Cold Spring Harbor Laboratory) · 2025
- <i>Sinorhizobium meliloti</i> BR-bodies promote fitness during host colonization
mBio · 2025
- Defining the role of RNase E in the mycobacterial degradosome-like network
bioRxiv (Cold Spring Harbor Laboratory) · 2025
- Stress Changes the Material State of a Bacterial Biomolecular Condensate and Shifts its Function from mRNA Decay to Storage
bioRxiv (Cold Spring Harbor Laboratory) · 2024
- Single-molecule dynamics in the internal environment of bacterial biomolecular condensates reveal cell-cycle-dependent differences in function
Biophysical Journal · 2024
- <i>Caulobacter crescentus</i> RNase E condensation contributes to autoregulation and fitness
Molecular Biology of the Cell · 2024
- TFIIB–Termination Factor Interaction Affects Termination of Transcription on Genome-Wide Scale
International Journal of Molecular Sciences · 2024
- <i>Sinorhizobium meliloti</i> BR-bodies promote fitness during host colonization
bioRxiv (Cold Spring Harbor Laboratory) · 2024
- Genome-wide analysis of TFIIB’s role in termination of transcription
bioRxiv (Cold Spring Harbor Laboratory) · 2024
- bioRxiv (Cold Spring Harbor Laboratory)×19
- Biophysical Journal×4
- Figshare×3
- Molecular Cell×2
- Proceedings of the National Academy of Sciences×2
This profile was generated automatically from public scholarly data (OpenAlex). Group size and activity levels are estimates derived from co-authorship patterns.
Last updated Jul 11, 2026.
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