水稻糯性相关基因的全基因组关联分析

利用1 090 071个SNP标记, 对419份广西地方稻种资源核心种质的糯性进行全基因组关联分析。结果表明, 运用混合线性模型, 在P<4.72×10^-8 (4.72E-8)水平下, 检测到45个与糯性显著关联的SNP位点, 均位于第6号染色体上。通过筛选显著关联位点上、下游各150 kb区域内的基因, 共找到305个候选基因, 其中包含2个与淀粉合成酶相关的Wx和SSIIa基因; 同时在第6号染色体5.69-5.89 Mb区域发现4个与糯性显著关联的SNP位点, 该区域可能是影响水稻(Oryza sativa)糯性的重要候选区域。     

Characterization of Nuclear Localization Signal in the N Terminus of Integrin-linked Kinase-associated Phosphatase (ILKAP) and Its Essential Role in the Down-regulation of RSK2 Protein Signaling

Integrin-linked kinase-associated phosphatase (ILKAP) is a serine/threonine (S/T) phosphatase that belongs to the protein phosphatase 2C (PP2C) family. Many previous studies have demonstrated that ILKAP plays key roles in the regulation of cell survival and apoptosis. Researchers have thus far considered ILKAP a cytoplasmic protein that negatively regulates integrin signaling by interacting with and phosphorylating integrin-linked kinase 1 (ILK1). In this study, we found that both endogenous and tagged ILKAP mainly localize to the nucleus and that the nuclear transport of ILKAP is nuclear localization signal (NLS) importin-mediated. The ILKAP protein interacts directly with importin α1, α3, and α5. The NLS in ILKAP is located in the N-terminal region between amino acids 71 and 86, and the NLS-deleted ILKAP protein was distributed in the cytoplasm. In addition, we show that Lys-78 and Arg-79 are critical for the binding of ILKAP to importin α. We also found that nuclear ILKAP interacts with ribosomal protein S6 kinase-2 (RSK2) and induces apoptosis by inhibiting RSK2 activity and down-regulating the expression level of the RSK2 downstream substrate cyclin D1. These results indicate that ILKAP is a nuclear protein that regulates cell survival and apoptosis through the regulation of RSK2 signaling.     

Neurogenic and Myogenic Properties of Pan-Colonic Motor Patterns and Their Spatiotemporal Organization in Rats

Background and Aims

Better understanding of intrinsic control mechanisms of colonic motility will lead to better treatment options for colonic dysmotility. The aim was to investigate neurogenic and myogenic control mechanisms underlying pan-colonic motor patterns.

Methods

Analysis of in vitro video recordings of whole rat colon motility was used to explore motor patterns and their spatiotemporal organizations and to identify mechanisms of neurogenic and myogenic control using pharmacological tools.

Results

Study of the pan-colonic spatiotemporal organization of motor patterns revealed: fluid-induced or spontaneous rhythmic propulsive long distance contractions (LDCs, 0.4–1.5/min, involving the whole colon), rhythmic propulsive motor complexes (RPMCs) (0.8–2.5/min, dominant in distal colon), ripples (10–14/min, dominant in proximal colon), segmentation and retrograde contractions (0.1–0.8/min, prominent in distal and mid colon). Spontaneous rhythmic LDCs were the dominant pattern, blocked by tetrodotoxin, lidocaine or blockers of cholinergic, nitrergic or serotonergic pathways. Change from propulsion to segmentation and distal retrograde contractions was most prominent after blocking 5-HT₃ receptors. In the presence of all neural blockers, bethanechol consistently evoked rhythmic LDC-like propulsive contractions in the same frequency range as the LDCs, indicating the existence of myogenic mechanisms of initiation and propulsion.

Conclusions

Neurogenic and myogenic control systems orchestrate distinct and variable motor patterns at different regions of the pan-colon. Cholinergic, nitrergic and serotonergic pathways are essential for rhythmic LDCs to develop. Rhythmic motor patterns in presence of neural blockade indicate the involvement of myogenic control systems and suggest a role for the networks of interstitial cells of Cajal as pacemakers.     

Culture of major pelvic ganglion neurons from adult rat

Successful culturing of neurons from adult animals has been historically difficult for a relatively long time. In this study, we reported the development of a novel method for the isolation and the culture of major pelvic ganglion (MPG) neurons from adult rat. The cultured cells were identified by neuron morphology and staining with neuronal marker (neurofilament-200, NF-200). The results demonstrate that the new protocol we used was reliable in obtaining a relatively high yield of MPG neurons. Furthermore, it improves the speed and simplicity in neuronal isolation. The viability of neurons can be maintained for about 2 weeks, which should be sufficient for investigating physiological and pathological processes occurring in mature major pelvic ganglia. And this may provide a useful assessment to currently available techniques for the culture of adult neurons.     

震旦鸦雀在镶嵌型芦苇收割生境中的巢址选择

大规模的芦苇收割会对在该生境中繁殖的鸟类产生严重影响。为降低芦苇收割对鸟类繁殖的负面影响,许多地区的湿地管理者逐渐采用了镶嵌型的芦苇收割方式。但是,这种新的芦苇管理方式对鸟类繁殖期生境选择的作用机理尚不清楚。震旦鸦雀是一种主要分布在我国东部、完全依赖芦苇生境而生存的珍稀鸟类,已被IUCN定为全球性近危物种。大规模的芦苇收割导致其适宜生境丧失,被认为是该物种面临的一个主要威胁。选择山东黄河三角洲国家级自然保护区为研究地区,采用AIC信息准则法,从巢址微生境、巢域斑块和全模型3个水平上对可能影响震旦鸦雀巢址选择的生境因子进行了逻辑斯蒂回归分析,并重点探讨芦苇镶嵌收割对其巢址选择的影响以及不同水平的相互效应。结果发现,震旦鸦雀的巢址选择受巢址微生境和巢域斑块尺度双重水平的影响,但巢址微生境因子的影响要大于巢域斑块因子。在巢址微生境水平上,影响震旦鸦雀巢址选择的因素有:1.5—2.5 m旧芦苇的密度、2.5 m以上新芦苇的密度、香蒲密度和巢的可见度;在巢域斑块水平上,影响因素包括芦苇生境类型、旧芦苇斑块面积的比例和植被盖度;在综合模型中,影响因素有1.5—2.5 m旧芦苇的密度、2.5 m以上新芦苇的密度、香蒲密度、巢的可见度和植被盖度。综上,震旦鸦雀倾向于在植被盖度较高、具有一定比例(18.3%)旧芦苇面积、1.5—2.5 m旧芦苇密度较高、可见度较低的生境斑块中筑巢。研究中,78.7%(n=141)的震旦鸦雀将巢筑在新旧芦苇混合的微生境中,其中36.9%的巢址附近旧芦苇的比例在一半以上;53.2%(n=111)的巢筑于新、旧两种芦苇茎秆之上,22.3%的巢的支撑芦苇中旧芦苇所占比例在一半以上。研究结果表明,旧芦苇在震旦鸦雀巢址选择和筑巢过程中发挥了重要作用。由于大范围的芦苇收割在微生境水平上可降低1.5—2.5 m旧芦苇的密度,在巢域斑块尺度上可降低旧芦苇斑块面积的比例,因此建议,在震旦鸦雀的繁殖地,未来的芦苇收割应采用镶嵌收割的形式,并至少应保留面积在20%以上的结构较好的旧芦苇斑块,以供震旦鸦雀选择巢址和繁衍后代。     

中国鳞翅目新物种2020年度报告

本文总结了2020年国内外学者发表的中国鳞翅目新分类单元的情况。经过统计, 2020年中国共发表鳞翅目新分类群196个, 其中新属1个, 新种190个, 新亚种5个; 发表国家级新记录71个; 发表新组合55个; 将11个名称处理为9个名称的异名; 新种(亚种)分别隶属于23个科。海南和云南两省发表的新物种数明显高于其他地区, 占全国新物种发表总数的2/5; 新记录种发表最多的地区为云南, 占全国新记录种总数的约1/2。整体来看, 我国南方新物种和新记录种发表数量明显高于北方。     

丛栽茶树树冠小气候及其对新梢生育和生化成分的影响

1 引言 为了获得优质高产的茶叶,需通过修剪养蓬等方法,使茶树形成宽广而整齐的树冠。丛栽茶树的树冠多呈馒头形,由于方位不同,形成了树冠内光、温、湿、风等因子的差异,因而影响了茶树的物候期及生理生化变化。因此,探讨树冠小气候特征及其对茶树新梢生育和生化成分的影响,在理论和生产实践上均有意义。有关这方面研究已有一些报道,但对茶树树冠小气候特征及其茶树新梢生育和品质成分的影响尚未见报     

Protein kinase C Theta inhibits insulin signaling by phosphorylating IRS1 at Ser(1101)

Obesity and stress inhibit insulin action by activating protein kinases that enhance serine phosphorylation of IRS1 and have been thus associated to insulin resistance and the development of type II diabetes. The protein kinase C (PKC) is activated by free-fatty acids, and its activity is higher in muscle from obese diabetic patients. However, a molecular link between PKC and insulin resistance has not been defined yet. Here we show that PKC phosphorylates IRS1 at serine 1101 blocking IRS1 tyrosine phosphorylation and downstream activation of the Akt pathway. Mutation of Ser(1101) to alanine makes IRS1 insensitive to the effect of PKC and restores insulin signaling in culture cells. These results provide a novel mechanism linking the activation of PKC to the inhibition of insulin signaling.     

氧自由基对大鼠心肌细胞核钙转运系统的影响

观察氧自由基对心肌细胞核钙转运系统的影响。方法;大鼠心肌细胞核采用蔗糖密度梯度心分离纯化,用酶学方法测定了ＡＴＰａｓｅ活性,用＾４５Ｃａ＾２＋同位素法测定下摄取。结果;低浓度的Ｈ２Ｏ２短时间作用使核钙泵活性增加３１．６％,高浓度Ｈ２Ｏ２使核钙泵活性降低,呈时间和剂量信赖性。     

Expression of SGTA correlates with neuronal apoptosis and reactive gliosis after spinal cord injury

Small glutamine-rich tetratricopeptide repeat (TPR)-containing protein alpha (SGTA) is a novel TPR-containing protein involved in various biological processes. However, the expression and roles of SGTA in the central nervous system remain unknown. We have produced an acute spinal cord injury (SCI) model in adult rats and found that SGTA protein levels first significantly increase, reach a peak at day 3 and then gradually return to normal level at day 14 after SCI. These changes are striking in neurons, astrocytes and microglia. Additionally, colocalization of SGTA/active caspase-3 has been detected in neurons and colocalization of SGTA/proliferating cell nuclear antigen has been detected in astrocytes and microglial. In vitro, SGTA depletion by short interfering RNA inhibits astrocyte proliferation and decreases cyclinA and cyclinD1 protein levels. SGTA knockdown also reduces neuronal apoptosis. We speculate that SGTA is involved in biochemical and physiological responses after SCI.