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1.
Figure 2

Figure 2. During cellular stress, hydrogel‐like assemblies form. From: Droplet organelles?.

(A) Stressors like heat shock, UV light, and transcription inhibition can cause cellular bodies to disassemble (CBs), change morphology (nucleoli, nuclear speckles), or appear de novo (stress bodies). (B) These granules contain proteins that form hydrogels and ultimately form an intricate proteinaceous network or aggregate (C). Micrographs reproduced from Hennig et al ().

Edward M Courchaine, et al. EMBO J. 2016 Aug 1;35(15):1603-1612.
2.
Figure 3

Figure 3. In disease, amyloid fibers arise from droplets. From: Droplet organelles?.

(A) Amyloid fibers can form in the nucleus or cytoplasm when constituent low‐complexity proteins are mutant. Concomitant changes in nuclear morphology have not been reported. (B) In vitro, fiber formation by mutant proteins, such as FUS, can follow droplet formation. Micrographs reproduced from Patel et al ().

Edward M Courchaine, et al. EMBO J. 2016 Aug 1;35(15):1603-1612.
3.
Figure 1

Figure 1. In homeostatic cellular conditions, dynamic fluid droplets demix from surrounding nucleoplasm. From: Droplet organelles?.

(A) Nucleoli, Cajal bodies (CBs), histone locus bodies (HLBs), speckles, and paraspeckles participate in RNA and RNP biogenesis in the nucleus. Associated with chromosomal loci, these nuclear bodies contain specific RNAs and proteins that pass in and out of nuclear bodies during RNP assembly. Unstable RNAs concentrate in P bodies in the cytoplasm, where mRNA decay factors co‐localize. (B) Analogous dynamics and fluid properties are obtained when a purified RNA‐binding protein with a low‐complexity region is incubated in with RNA and observed over time in vitro. (C) Electron micrograph of a droplet showing overall spherical shape with an irregular outline. Micrographs reproduced from Li et al ().

Edward M Courchaine, et al. EMBO J. 2016 Aug 1;35(15):1603-1612.

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