油葵苗期抗旱相关性状的QTL定位及候选基因筛选

干旱是限制向日葵生长发育的重要因素之一。为探究向日葵苗期抗旱性分子机制,该研究以向日葵K55与K58杂交构建的150个F₇重组自交系群体为材料,对其在正常浇水和干旱胁迫两种水分处理条件下的叶片相对电导率、叶绿素含量、叶面积、叶片相对含水量、根长进行表型测定,利用前期建立的SNP、SSR分子标记遗传连锁图谱,通过复合区间作图法对5个抗旱相关的性状进行QTL定位。结果表明：(1)共定位到向日葵QTL位点11个,其中正常浇水条件下5个,干旱胁迫条件下6个,表型贡献率为0.768%~7.547%,且5号连锁群上定位到的QTL位点最多(3个)。(2)QTL置信区间内共筛选到62个与干旱相关的候选基因,包括位于qLA 8 1上的rna23019、rna23004、rna22661、rna22193、rna23294、rna22783和位于qCC 13 1上的rna40140,这些基因可作为后续基因克隆及功能研究的重点候选基因。该研究结果为向日葵抗旱性研究及其遗传改良奠定了基础。     

四川贡嘎山国家级自然保护区鸟兽多样性

四川贡嘎山国家级自然保护区位于全球生物多样性热点地区之一的横断山区, 是我国生物多样性保护优先区。本文利用红外相机影像和已发表文献对该保护区的大中型兽类和地面活动鸟类进行编目并提出未来监测建议。2011-2018年在97个1 km × 1 km的网格安放红外相机, 累计39,881个相机日, 获得独立有效照片20,932张, 其中野生兽类16,244张, 鸟类2,775张, 牲畜1,737张, 人176张。鉴定出野生兽类30种, 另有文献报道4种和观察3种, 分属于5目15科; 鸟类78种, 分属于9目22科; 牲畜6种。包括12种国家I级和28种国家II级重点保护野生动物; 被CITES附录I收录的有11种, 附录II收录的有12种。被IUCN红色名录评估为濒危(EN)和易危(VU)等级的分别有3种和8种。被《中国脊椎动物红色名录》评估为极危(CR)、濒危和易危等级的分别有5、5和11种。相对多度指数(relative abundance index, RAI)排名前三的兽类是毛冠鹿(Elaphodus cephalophus, 147.39)、水鹿(Rusa unicolor, 66.10)、野猪(Sus scrofa, 36.03); 鸟类是血雉(Ithaginis cruentus, 14.64)、白马鸡(Crossoptilon crossoptilon, 10.43)、大噪鹛(Garrulax maximus, 8.05)。阔叶林、针阔混交林、高山灌丛草甸和高山流石滩是调查薄弱生境, 后期应开展重点调查, 以厘清本区域大中型兽类资源。     

典型黑土区农田土壤线虫群落的纬度分布格局及其驱动机制

东北黑土区是保障我国粮食安全的重要土壤资源, 了解该区域内农田土壤线虫的群落组成及其对环境驱动因子的响应机制, 对于研究黑土区农田土壤生态系统的生物多样性分布格局具有重要意义。2018年9月, 我们在42°50°‒49°08° N的典型黑土区采集了93个农田土壤样品, 利用形态学鉴定技术分析了土壤线虫群落的组成与结构。共鉴定出47个线虫属(相对丰度 > 1%), 其中食细菌线虫中的拟丽突属(Acrobeloides)是典型黑土区农田土壤中的优势属(相对丰度 > 5%)。土壤线虫总丰富度和总多度均随纬度增加而显著增加, 然而类似的变化趋势只出现在食细菌和杂食/捕食线虫中。土壤有机碳是影响土壤线虫丰富度和多度最为重要的环境因子, 其次是月平均温度。典型黑土区农田土壤线虫群落结构以47° N为分界线分为南部和北部两类, 主要归因于线虫群落中植物寄生和杂食/捕食线虫的相对多度在南、北特征属中存在差异。土壤pH值和容重分别是影响南部与北部黑土区线虫群落最重要的环境因子。本研究明确了典型黑土区农田土壤线虫群落的纬度分布格局及其与环境因素的关系, 可为揭示农业活动干扰下土壤生物对环境因子的响应机制提供基础数据和理论参考。     

Identification of SOCS5 Gene in the Chinese Giant Salamander (Andrias davidianus) and Expression Profiles in Response to Citrobacter freundii Challenge

Russian Journal of Bioorganic Chemistry - The full-length cDNA sequences of suppressor of cytokine signaling 5 (SOCS5) from Andrias davidianus gene, named as adSOCS5, was cloned and characterized...     

Pulsed electromagnetic fields regulate osteocyte apoptosis,RANKL/OPG expression,and its control of osteoclastogenesis depending on the presence of primary cilia

Growing evidence has shown that pulsed electromagnetic fields (PEMF) can modulate bone metabolism in vivo and regulate the activities of osteoblasts and osteoclasts in vitro. Osteocytes, accounting for 95% of bone cells, act as the major mechanosensors in bone for transducing external mechanical signals and producing cytokines to regulate osteoblastic and osteoclastic activities. Targeting osteocytic signaling pathways is becoming an emerging therapeutic strategy for bone diseases. We herein systematically investigated the changes of osteocyte behaviors, functions, and its regulation on osteoclastogenesis in response to PEMF. The osteocyte-like MLO-Y4 cells were exposed to 15 Hz PEMF stimulation with different intensities (0, 5, and 30 Gauss [G]) for 2 hr. We found that the cell apoptosis and cytoskeleton organization of osteocytes were regulated by PEMF with an intensity-dependent manner. Moreover, PEMF exposure with 5 G significantly inhibited apoptosis-related gene expression and also suppressed the gene and protein expression of the receptor activator of nuclear factor κB ligand/osteoprotegerin (RANKL/OPG) ratio in MLO-Y4 cells. The formation, maturation, and osteoclastic bone-resorption capability of in vitro osteoclasts were significantly suppressed after treated with the conditioned medium from PEMF-exposed (5 G) osteocytes. Our results also revealed that the inhibition of osteoclastic formation, maturation, and bone-resorption capability induced by the conditioned medium from 5 G PEMF-exposed osteocytes was significantly attenuated after abrogating primary cilia in osteocytes using the polaris siRNA transfection. Together, our findings highlight that PEMF with 5 G can inhibit cellular apoptosis, modulate cytoskeletal distribution, and decrease RANKL/OPG expression in osteocytes, and also inhibit osteocyte-mediated osteoclastogenesis, which requires the existence of primary cilia in osteocytes. This study enriches our basic knowledge for further understanding the biological behaviors of osteocytes and is also helpful for providing a more comprehensive mechanistic understanding of the effect of electromagnetic stimulation on bone and relevant skeletal diseases (e.g., bone fracture and osteoporosis).     

UHRF1 is regulated by miR-124-3p and promotes cell proliferation in intrahepatic cholangiocarcinoma

Ubiquitin-like with PHD and ring finger domains 1 (UHRF1) is abnormally overexpressed in multiple cancers and closely correlated with tumor-promoting effects, such as high proliferation. However, how UHRF1 functions in intrahepatic cholangiocarcinoma (ICC) has not yet been determined. Herein, we found that UHRF1 is overexpressed in ICC tissues. Downregulated UHRF1 attenuated the transition of the G1/S cell cycle and then suppressed cell proliferation in vitro and tumor growth in vivo. Moreover, upstream regulators of the UHRF1 expression were predicted, and we found that direct binding of miR-124-3p inhibited the UHRF1 expression. Elevated miR-124-3p suppressed proliferation and led to the arrest of the cell cycle. Furthermore, the expression of UHRF1 was positively correlated with PCNA. Clinically, we showed that elevated UHRF1 was associated with poor prognosis, and served as an independent prognostic factor in ICC patients. Together, these findings demonstrate that UHRF1, regulated by miR-124-3p, acts as a tumor promoter by promoting cell proliferation in ICC.     

Quercetin relieved diabetic neuropathic pain by inhibiting upregulated P2X4 receptor in dorsal root ganglia

The upregulation of nociceptive ion channels expressed in dorsal root ganglia (DRG) contributes to the development and retaining of diabetic pain symptoms. The flavonoid quercetin (3,3′,4′,5,7-pentahydroxyflavone) is a component extracted from various fruits and vegetables and exerts anti-inflammatory, analgesic, anticarcinogenic, antiulcer, and antihypertensive effects. However, the exact mechanism underlying quercetin's analgesic action remains poorly understood. The aim of this study was to investigate the effects of quercetin on diabetic neuropathic pain related to the P2X₄ receptor in the DRG of type 2 diabetic rat model. Our data showed that both mechanical withdrawal threshold and thermal withdrawal latency in diabetic rats treated with quercetin were higher compared with those in untreated diabetic rats. The expression levels of P2X₄ messenger RNA and protein in the DRG of diabetic rats were increased compared with the control rats, while quercetin treatment significantly inhibited such enhanced P2X₄ expression in diabetic rats. The satellite glial cells (SGCs) enwrap the neuronal soma in the DRG. Quercetin treatment also lowered the elevated coexpression of P2X₄ and glial fibrillary acidic protein (a marker of SGCs) and decreased the upregulation of phosphorylated p38 mitogen-activated protein kinase (p38MAPK) in the DRG of diabetic rats. Quercetin significantly reduced the P2X₄ agonist adenosine triphosphate-activated currents in HEK293 cells transfected with P2X₄ receptors. Thus, our data demonstrate that quercetin may decrease the upregulation of the P2X₄ receptor in DRG SGCs, and consequently inhibit P2X₄ receptor-mediated p38MAPK activation to relieve the mechanical and thermal hyperalgesia in diabetic rats.