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Genomic competition for noise reduction shaped evolutionary landscape of mir-4673

机译:降噪的基因组竞争塑造了Mir-4673的进化景观

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摘要

Structural analysis shows improved thermodynamic stability of the RNA hairpin in the primate lineage culminating in structural maturation of the miR-4673 hairpin in . Nucleosome-favouring dinucleotide usage map of human notch-1 intron 4. Transmission electron micrograph of a nucleosome formed by NPS (left). Gel retardation (middle) and restriction enzyme digestion assays (right) provided further confirmation for nucleosome formation by NPS . The temporal profile of enhancer-RNAs (eRNAs) that originate from notch-1 intron-4 (full blots are provided in Supplementary Fig. ). Vertical lines show the location of eRNAs with reference to the dinucleotide usage map. In order to access the eRNA profile, cells were synchronised at G0 and released into G1 by application of a single pulse of FGF-2. Note the temporal stability of 3′-eRNA from a region that corresponds to NPS (see Supplementary Fig. ). This region is positioned at the 3′-terminus of a stable RNA palindrome formed by two Alu elements. Histogram shows cumulative distribution of TCF3/4 and TFAP2A/B/C -motifs in the intron 4 of human notch-1. At the bottom, Levenshtein distance (L.E.D) as a measure of intronic change is aligned to the enhancer map. Sequences that belong to AluJb and AluYa1 insertions in all Simians are in grey. Species-specific transpositional events are marked in LED heat maps.
机译:结构分析显示改善了灵长类谱系中RNA发夹的热力学稳定性,最终导致了miR-4673发夹的结构成熟。人类notch-1内含子的核小体偏爱二核苷酸使用图。NPS形成的核小体的透射电子显微照片(左)。凝胶阻滞(中)和限制酶消化试验(右)为通过NPS形成核小体提供了进一步的确认。源于notch-1 intron-4的增强子RNA(eRNA)的时间变化(完整的印迹在补充图中提供)。垂直线相对于二核苷酸使用图显示了eRNA的位置。为了访问eRNA图谱,将细胞在G0处同步,并通过施加单个FGF-2脉冲释放到G1中。注意来自与NPS相对应的区域的3'-eRNA的时间稳定性(参见补充图)。该区域位于由两个Alu元件形成的稳定的RNA回文序列的3'末端。直方图显示了人notch-1内含子4中TCF3 / 4和TFAP2A / B / C-基序的累积分布。底部的Levenshtein距离(L.E.D)作为内含子变化的量度与增强子图对齐。在所有猿猴中属于AluJb和AluYa1插入的序列均为灰色。特定于物种的转座事件在LED热图中标记。

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