共查询到20条相似文献,搜索用时 8 毫秒
1.
2.
3.
4.
Camilla Pramfalk Tiffany A. Melhuish David Wotton Zhao-Yan Jiang Mats Eriksson Paolo Parini 《Journal of lipid research》2014,55(4):709-717
Acat2 [gene name: sterol O-acyltransferase 2 (SOAT2)] esterifies cholesterol in enterocytes and hepatocytes. This study aims to identify repressor elements in the human SOAT2 promoter and evaluate their in vivo relevance. We identified TG-interacting factor 1 (Tgif1) to function as an important repressor of SOAT2. Tgif1 could also block the induction of the SOAT2 promoter activity by hepatocyte nuclear factor 1α and 4α. Women have ∼30% higher hepatic TGIF1 mRNA compared with men. Depletion of Tgif1 in mice increased the hepatic Soat2 expression and resulted in higher hepatic lipid accumulation and plasma cholesterol levels. Tgif1 is a new player in human cholesterol metabolism. 相似文献
5.
6.
7.
8.
9.
10.
11.
《Developmental cell》2022,57(16):2009-2025.e6
- Download : Download high-res image (119KB)
- Download : Download full-size image
12.
13.
14.
XiangSong Wu Fang Wang HuaiFeng Li YunPing Hu Lin Jiang Fei Zhang MaoLan Li XuAn Wang YunPeng Jin YiJian Zhang Wei Lu WenGuang Wu YiJun Shu Hao Weng Yang Cao RunFa Bao HaiBin Liang Zheng Wang YiChi Zhang Wei Gong Lei Zheng ShuHan Sun YingBin Liu 《EMBO reports》2022,23(9)
Correction to: EMBO Reports (2017) 18: 1837–1853. DOI: 10.15252/embr.201744147 ¦ Published online 8 September 2017The authors contacted the journal after becoming aware of duplications between Figs 3 and 6 and identified additional errors in the process of reanalysing their data. Figure 3B: The authors state that the representative images of the migration and invasion assays of EH‐GB1 cells in the Lv‐Control groups had been incorrectly selected from images belonging to the control groups. The figure is herewith corrected. Figure 6B: The authors state that they had incorrectly displayed representative images for the vector group of SGC‐996, and the vector and PAGBC‐mut (miR‐133b) groups of EH‐GB1. The figure is herewith corrected.In addition, the authors are adding a demarcating line to the PCR product of the 5′‐RACE in Fig EV2B, separating the marker lane, which had been inadvertently omitted. Source data for Fig EV2 were published in the original paper.The source data and replicate data for Figs 3B and 6B are published with this corrigendum.The authors apologize for this oversight and any confusion it may have caused and declare that the conclusions of the study are not affected by these changes. 相似文献
15.
16.
In this work, we conducted functional analysis of Arabidopsis HRS1 gene in order to provide new insights into the mechanisms governing seed germination. Compared with wild type (WT) control, HRS1 knockout mutant (hrs1-1) exhibited significant germination delays on either normal medium or those supplemented with abscisic acid (ABA) or sodium chloride (NaCl), with the magnitude of the delay being substantially larger on the latter media. The hypersensitivity of hrs1-1 germination to ABA and NaCl required ABI3, ABI4 and ABI5, and was aggravated in the double mutant hrs1-1abi1-2 and triple mutant hrs1-1hab1-1abi1-2, indicating that HRS1 acts as a negative regulator of ABA signaling during seed germination. Consistent with this notion, HRS1 expression was found in the embryo axis, and was regulated both temporally and spatially, during seed germination. Further analysis showed that the delay of hrs1-1 germination under normal conditions was associated with reduction in the elongation of the cells located in the lower hypocotyl (LH) and transition zone (TZ) of embryo axis. Interestingly, the germination rate of hrs1-1 was more severely reduced by the inhibitor of cell elongation, and more significantly decreased by the suppressors of plasmalemma H(+)-ATPase activity, than that of WT control. The plasmalemma H(+)-ATPase activity in the germinating seeds of hrs1-1 was substantially lower than that exhibited by WT control, and fusicoccin, an activator of this pump, corrected the transient germination delay of hrs1-1. Together, our data suggest that HRS1 may be needed for suppressing ABA signaling in germinating embryo axis, which promotes the timely germination of Arabidopsis seeds probably by facilitating the proper function of plasmalemma H(+)-ATPase and the efficient elongation of LH and TZ cells. 相似文献
17.
18.
19.
Stavroula Tsaridou Georgia Velimezi Frances Willenbrock Maria Chatzifrangkeskou Waheba Elsayed Andreas Panagopoulos Dimitris Karamitros Vassilis Gorgoulis Zoi Lygerou Vassilis Roukos Eric O'Neill Dafni Eleftheria Pefani 《EMBO reports》2022,23(8)
DNA lesions occur across the genome and constitute a threat to cell viability; however, damage at specific genomic loci has a relatively greater impact on overall genome stability. The ribosomal RNA gene repeats (rDNA) are emerging fragile sites. Recent progress in understanding how the rDNA damage response is organized has highlighted a key role of adaptor proteins. Here, we show that the scaffold tumor suppressor RASSF1A is recruited to rDNA breaks. RASSF1A recruitment to double‐strand breaks is mediated by 53BP1 and depends on RASSF1A phosphorylation at Serine 131 by ATM kinase. Employing targeted rDNA damage, we uncover that RASSF1A recruitment promotes local ATM signaling. RASSF1A silencing, a common epigenetic event during malignant transformation, results in persistent breaks, rDNA copy number alterations and decreased cell viability. Overall, we identify a novel role for RASSF1A at rDNA break sites, provide mechanistic insight into how the DNA damage response is organized in a chromatin context, and provide further evidence for how silencing of the RASSF1A tumor suppressor contributes to genome instability. 相似文献
20.