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One important mode of gene regulation is miRNA-mediated post-transcriptional mRNA transcript repression.
IGS transcript repression requires proteins of the heterochromatic siRNA pathway, including RNA polymerase IV (Pol IV), RNA-DEPENDENT RNA POLYMERASE 2 (RDR2) and DICER-LIKE 3 (DCL3).
Beyond 5S rDNA transcript repression, RNA silencing proteins and DDM1 are both required for full condensation of 5S rDNA repeats in the nucleus.
This distance is similar to that reported from Drosophila, where spread of silencing from transposons to active genes occurs, leading to transcript repression.
The investigation of average chromatin profiles around repressed and expressed RTSSs has revealed a subtle relationship between open and closed chromatin, and between transcript repression and expression.
The summary plot of the query (seed) distribution (See Figure 1B) is a useful representation of the differential distribution of a query sequence and, by inference, an estimate of the magnitude and location of transcript repression in a given dataset.
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Among the cell wall related transcripts, repression of β-1,3-glucan synthase associated to callose biosynthesis.
Sugar reduces miR156 abundance through both transcriptional repression and transcript degradation.
Plant microRNAs (miRNAs) are involved in multiple developmental and physiological processes and negatively regulate gene transcript abundance through post-transcriptional repression of mRNAs, primarily by target cleavage [1].
Transcriptional repression of respiratory transcripts in Cabernet Sauvignon probably functions to reduce ROS production.
Taken together these studies reveal hypoxia-dependent repression of Cx43 transcript in conjunction with increased phosphorylation of Cx43-Serine368, suggesthat thypoxiaoxiattenuatesendothelialiATPATP release by transcriptional repression and phosphorylation of Cx43.
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