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Figure 2.

Figure 2.Stress can cause heritable changes in chromatin structure and biochemistry.. From: Mechanisms for the epigenetic inheritance of stress response in single cells.

Activated protein kinases can directly or indirectly change epigenetic marks on DNA and histones. Stress response can also change the 3D structure of chromatin. If sufficiently stable, these epigenetic changes can be heritable by daughter cells, corresponding to passing an ‘epigenetic memory’ of mother’s specific transcriptional states. p: phosphorylation; Me: Methylation; Ac: Acetylation.

Yuan Xue, et al. Curr Genet. ;64(6):1221-1228.
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Figure 3.

Figure 3.Cell division and cell-to-cell fusion propagate stress response to descendants.. From: Mechanisms for the epigenetic inheritance of stress response in single cells.

A. Anti-stress proteins, mRNAs and miRNAs are passed on to daughter cells during cell division. B. Asymmetrical segregation of damaged molecules generates a ‘damage-protected’ daughter cell at the expense of the mother cell’s being burdened with more damage. C. Sperm carrying miRNAs produced as a result of stress-induction transmits the stress signal to an oocyte during fertilization.

Yuan Xue, et al. Curr Genet. ;64(6):1221-1228.
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Figure 1.

Figure 1.Stress induces dynamic changes in Msn2 nuclear localization.. From: Mechanisms for the epigenetic inheritance of stress response in single cells.

A. In response to various stress stimuli, Msn2 proteins become dephosphorylated and translocate into the nucleus to activate downstream gene expression. PP1: Protein phosphatase 1, PKA: cAMP-dependent protein kinase A, STRE: stress response element. B. Msn2 nuclear localization trajectory of a cell, showing how amplitude, frequency, and duration of Msn2 nuclear localization are quantified. The dashed horizontal line denotes the threshold level above which there would be an Msn2 nuclear localization event. ni denotes the number of above-the-threshold localization events. T denotes the length of time interval used for the calculation of frequency. Figure panel was taken from .

Yuan Xue, et al. Curr Genet. ;64(6):1221-1228.

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