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971.
Lu Fu Yao Sun Yongqing Guo Yan Chen Bin Yu Haihong Zhang Jiaxin Wu Xianghui Yu Wei Kong Hui Wu 《Journal of peptide science》2017,23(3):245-251
The abnormal deposition of amyloid‐β (Aβ) peptides in the brain is the main neuropathological hallmark of Alzheimer's disease (AD). Amyloid deposits are formed by a heterogeneous mixture of Aβ peptides, among which the most studied are Aβ40 and Aβ42. Aβ40 is abundantly produced in the human brain, but the level of Aβ42 is remarkably increased in the brain of AD patients. Aside from Aβ40 and Aβ42, recent data have raised the possibility that Aβ43 peptides may be instrumental in AD pathogenesis. Besides its length, whether the Aβ aggregated form accounts for the neurotoxicity is also particularly controversial. Aβ fibrils are generally considered as key pathogenic substances in AD pathogenesis. Nevertheless, recent data implicated soluble Aβ oligomers as the main cause of synaptic dysfunction and memory loss in AD. To further address this uncertainty, we analyzed the neurotoxicity of different Aβ species and Aβ forms at the cellular level. The results showed that Aβ42 could form oligomers significantly faster than Aβ40 and Aβ43 and Aβ42 oligomers showed the greatest level of neurotoxicity. Regardless of the length of Aβ peptides, Aβ oligomers induced significantly higher cytotoxicity compared with the other two Aβ forms. Surprisingly, the neurotoxicity of fibrils in PC12 cells was only marginally but not significantly stronger than monomers, contrary to previous reports. Altogether, our findings demonstrate the high pathogenicity of Aβ42 among the three Aβ species and support the idea that Aβ42 oligomers contribute to the pathological events leading to neurodegeneration in AD. Copyright © 2017 European Peptide Society and John Wiley & Sons, Ltd. 相似文献
972.
Huayan Yin Xuye Du Biao Wang Xin Ma Cunyao Bo Anfei Li Xiaocun Zhang Lingrang Kong 《Molecular breeding : new strategies in plant improvement》2017,37(8):97
High-molecular-weight glutenin subunits (HMW-GS) in wheat grain are the major determinants of dough elasticity and viscosity and thus of bread-making quality. PCR-based molecular markers designed based on DNA polymorphisms were used to analyze HMW-GS genes in wheat. The loop-mediated isothermal amplification (LAMP) assay is a simple and rapid method for specific detection of genomic DNA target sequences. In the present study, we designed a set of LAMP markers by targeting the unique sequences of 1Dx2 and 1Dx5 genes. The primers could effectively distinguish the 1Dx2 and 1Dx5 genes from other genes at the Glu-1 locus. The results were confirmed by agarose gel electrophoresis. For visualization, ethidium bromide was used, and fluorescence only appeared in the positive samples. Under optimal conditions, the detection could be finished in 1 h. Thirty-eight wheat cultivars with known HMW-GS were used to validate LAMP markers for 1Dx2 and 1Dx5 genes. Only DNA samples with target genes could be amplified, and the results could be read easily using this method. The tests using LAMP were easy to perform, rapid, and sensitive. Thus, the current study results have the potential to be a powerful tool for the detection of HMW-GS genes in wheat. 相似文献
973.
Na Li Haiyan Jia Zhongxin Kong Wenbin Tang Yunxiao Ding Junchao Liang Hongqi Ma Zhengqiang Ma 《Molecular breeding : new strategies in plant improvement》2017,37(6):79
Powdery mildew, a wheat (Triticum aestivum L.) foliar disease caused by Blumeria graminis (DC.) E.O. Speer f. sp. tritici, imposes a constant challenge on wheat production in areas with cool or maritime climates. This study was conducted to identify and transfer the resistance gene in the newly identified common wheat accession ‘D29’. Genetic analysis of the F2 population derived from a cross of D29 with the susceptible elite cultivar Y158 suggested a single dominant gene is responsible for the powdery mildew resistance in this germplasm. This gene was mapped to chromosome 2AL in a region flanked by microsatellite markers Xgdm93 and Xhbg327, and co-segregated with sequence-tagged site (STS) markers Xsts_bcd1231 and TaAetPR5. An allelic test indicated that the D29 gene was allelic to the Pm4 locus. To further evaluate the resistance conferred by this gene and develop new germplasms for breeding, this gene, as well as Pm4a and Pm4b, was transferred to Y158 through backcross and marker-assisted selection. In the resistance spectrum analysis, the D29 gene displayed a resistance spectrum distinguishable from the other Pm4 alleles, including Pm4a, Pm4b, and Pm4c, and thus was designated as Pm4e. The identification of new allelic variation at the Pm4 locus is important for understanding the resistance gene evolution and for breeding wheat cultivars with powdery mildew resistance. 相似文献
974.
基于直接接触的微生物胞外电子传递 总被引:1,自引:1,他引:0
微生物电子传递在微生物的代谢繁殖和物质的生物地球化学循环中发挥着关键作用。其中基于直接接触的微生物胞外电子传递(Direct extracellular electron transfer,DEET)已成为微生物学、地球化学和生物物理学等学科共同关注的焦点,并在近几年取得了一系列重要发现和理论突破,包括微生物纳米导线、电缆细菌、微生物种间DEET等。伴随着这些新进展,更多的问题也需要研究者们在进一步的研究中解决,包括DEET的分子机制及其相关功能微生物种群等。不同学科理论和技术的交叉是进一步揭示DEET过程的关键。 相似文献
975.
Lilin Zhu Zhicheng Xiong Wei Yu Xiaolin Tian Yan Kong Cheng Liu Shouyu Wang 《Plasmonics (Norwell, Mass.)》2017,12(1):33-38
A polarization-controlled tunable plasmonic lens which can generate different multi-focal combinations with exciting sources of left and right circular polarizations is proposed in this paper. Both position and intensity of each focal point can be adjusted by modulating the structure of the plasmonic lens. It is believed that the polarization-controlled tunable plasmonic multi-focal lens can be potentially used for optical switches and multi-channel couplers in future logic photonic and plasmonic systems. 相似文献
976.
Perinatal transmission of Human immunodeficiency virus(HIV),also called mother-to-child transmission(MTCT),accounts for 90% of infections in infants worldwide and occurs in 30%-45% of children born to untreated HIV-1 infected mothers.Among HIV-1 infected mothers,some viruses are transmitted from mothers to their infants while others are not.The relationship between virologic properties and the pathogenesis caused by HIV-1 remains unclear.Previous studies have demonstrated that one obvious source of selective pressure in the perinatal transmission of HIV-1 is maternal neutralizing antibodies.Recent studies have shown that viruses which are successfully transmitted to the child have growth advantages over those not transmitted,when those two viruses are grown together.Furthermore,the higher fitness is determined by the gp120 protein of the virus envelope.This suggests that the selective transmission of viruses with higher fitness occurred exclusively,regardless of transmission routes.There are many factors contributing to the selective transmission and HIV replicative fitness is an important one that should not be neglected.This review summarizes current knowledge of the role of HIV replicative fitness in HIV MTCT transmission and the determinants of viral fitness upon MTCT. 相似文献
977.
2009年中国植物科学在水稻和拟南芥研究等方面取得“爆发性”的快速发展。中国科学家在植物科学各领域中取得了大量的原创性研究成果, 尤其是在基于新一代测序技术和计算生物学理论的基因组学、水稻功能基因挖掘、激素受体和信号转导以及转基因作物产业化和生态安全性研究等方面取得一系列重大进展, 受到了国内外广泛关注。该文对2009年中国本土植物生命科学若干领域取得的重要研究进展进行概括性评述, 旨在全面追踪当前中国植物科学领域发展的最新前沿和热点事件, 并展现我国科学家们所取得的杰出成就。 相似文献
978.
Wenqing Zhang Ronghui Zhou Yuting Yang Shuanglin Peng Dexuan Xiao Tingting Kong Xiaoxiao Cai Bofeng Zhu 《Cell proliferation》2021,54(9)
ObjectivesThe nano‐hydroxyapatite (nHAp) is widely used to develop imaging probes and drug carriers due to its excellent bioactivity and biocompatibility. However, traditional methods usually need cumbersome and stringent conditions such as high temperature and post‐modification to prepare the functionalized nHAp, which do not benefit the particles to enter cells due to the increased particle size. Herein, a biomimetic synthesis strategy was explored to achieve the AS1411‐targeted tumour dual‐model bioimaging using DNA aptamer AS1411 as a template. Then, the imaging properties and the biocompatibility of the synthesized AS‐nFAp:Gd/Tb were further investigated.Materials and methodsThe AS‐nFAp:Gd/Tb was prepared under mild conditions through a one‐pot procedure with AS1411 as a template. Besides, the anticancer drug DOX was loaded to AS‐nFAp:Gd/Tb so as to achieve the establishment of a multifunctional nano‐probe that integrated the tumour diagnosis and treatment. The AS‐nFAp:Gd/Tb was characterized by transmission electron microscopy (TEM), energy disperse X‐ray Spectroscopy (EDS) mapping, X‐ray photoelectron spectroscopy (XPS) spectrum, X‐ray diffraction (XRD), fourier‐transformed infrared (FTIR) spectroscopy, capillary electrophoresis analyses, zeta potential and particle sizes. The in vitro magnetic resonance imaging (MRI) and fluorescence imaging were performed on an MRI system and a confocal laser scanning microscope, respectively. The potential of the prepared multifunctional nHAp for a targeted tumour therapy was investigated by a CCK‐8 kit. And the animal experiments were conducted on the basis of the guidelines approved by the Animal Care and Use Committee of Sichuan University, China.ResultsIn the presence of AS1411, the as‐prepared AS‐nFAp:Gd/Tb presented a needle‐like morphology with good monodispersity and improved imaging performance. Furthermore, due to the specific binding between AS1411 and nucleolin up‐expressed in cancer cells, the AS‐nFAp:Gd/Tb possessed excellent AS1411‐targeted fluorescence and MRI imaging properties. Moreover, after loading chemotherapy drug DOX, in vitro and in vivo studies showed that DOX@AS‐nFAp:Gd/Tb could effectively deliver DOX to tumour tissues and exert a highly effective tumour inhibition without systemic toxicity compared with pure DOX.ConclusionsThe results indicated that the prepared multifunctional nHAp synthesized by a novel biomimetic strategy had outstanding capabilities of recognition and treatment for the tumour and had good biocompatibility; hence, it might have a potential clinical application in the future. 相似文献
979.
980.
Li Yu Dachuan Shi Junling Li Yingzhen Kong Yanchong Yu Guohua Chai Ruibo Hu Juan Wang Michael G. Hahn Gongke Zhou 《Plant physiology》2014,164(4):1842-1856
Mannans are hemicellulosic polysaccharides that are considered to have both
structural and storage functions in the plant cell wall. However, it is not yet known
how mannans function in Arabidopsis (Arabidopsis thaliana) seed
mucilage. In this study, CELLULOSE SYNTHASE-LIKE A2
(CSLA2; At5g22740) expression was observed in several seed
tissues, including the epidermal cells of developing seed coats. Disruption of
CSLA2 resulted in thinner adherent mucilage halos, although the
total amount of the adherent mucilage did not change compared with the wild type.
This suggested that the adherent mucilage in the mutant was more compact compared
with that of the wild type. In accordance with the role of CSLA2 in glucomannan
synthesis, csla2-1 mucilage contained 30% less mannosyl and glucosyl
content than did the wild type. No appreciable changes in the composition, structure,
or macromolecular properties were observed for nonmannan polysaccharides in mutant
mucilage. Biochemical analysis revealed that cellulose crystallinity was
substantially reduced in csla2-1 mucilage; this was supported by the
removal of most mucilage cellulose through treatment of csla2-1
seeds with endo-β-glucanase. Mutation in CSLA2 also resulted
in altered spatial distribution of cellulose and an absence of birefringent cellulose
microfibrils within the adherent mucilage. As with the observed changes in
crystalline cellulose, the spatial distribution of pectin was also modified in
csla2-1 mucilage. Taken together, our results demonstrate that
glucomannans synthesized by CSLA2 are involved in modulating the structure of
adherent mucilage, potentially through altering cellulose organization and
crystallization.Mannan polysaccharides are a complex set of hemicellulosic cell wall polymers that are
considered to have both structural and storage functions. Based on the particular chemical
composition of the backbone and the side chains, mannan polysaccharides are classified into
four types: pure mannan, glucomannan, galactomannan, and galactoglucomannan (Moreira and Filho, 2008; Wang et al., 2012; Pauly et al.,
2013). Each of these polysaccharides is composed of a β-1,4-linked
backbone containing Man or a combination of Glc and Man residues. In addition, the mannan
backbone can be substituted with side chains of α-1,6-linked Gal residues. Mannan
polysaccharides have been proposed to cross link with cellulose and other hemicelluloses
via hydrogen bonds (Fry, 1986; Iiyama et al., 1994; Obel et al., 2007; Scheller and
Ulvskov, 2010). Furthermore, it has been reported that heteromannans with
different levels of substitution can interact with cellulose in diverse ways (Whitney et al., 1998). Together, these observations
indicate the complexity of mannan polysaccharides in the context of cell wall
architecture.CELLULOSE SYNTHASE-LIKE A (CSLA) enzymes have been shown to have mannan synthase activity
in vitro. These enzymes polymerize the β-1,4-linked backbone of mannans or
glucomannans, depending on the substrates (GDP-Man and/or GDP-Glc) provided (Richmond and Somerville, 2000; Liepman et al., 2005, 2007;
Pauly et al., 2013). In Arabidopsis
(Arabidopsis thaliana), nine CSLA genes have been
identified; different CSLAs are responsible for the synthesis of different
mannan types (Liepman et al., 2005, 2007). CSLA7 has mannan synthase activity in vitro
(Liepman et al., 2005) and has been shown to
synthesize stem glucomannan in vivo (Goubet et al.,
2009). Disrupting the CSLA7 gene results in defective pollen
growth and embryo lethality phenotypes in Arabidopsis, indicating structural or signaling
functions of mannan polysaccharides during plant embryo development (Goubet et al., 2003). A mutation in CSLA9 results in
the inhibition of Agrobacterium tumefaciens-mediated root transformation
in the rat4 mutant (Zhu et al.,
2003). CSLA2, CSLA3, and CSLA9 are proposed to play nonredundant roles in the
biosynthesis of stem glucomannans, although mutations in CSLA2,
CSLA3, or CSLA9 have no effect on stem development or
strength (Goubet et al., 2009). All of the
Arabidopsis CSLA proteins have been shown to be involved in the biosynthesis of mannan
polysaccharides in the plant cell wall (Liepman et al.,
2005, 2007), although the precise
physiological functions of only CSLA7 and CSLA9 have been conclusively demonstrated.In Arabidopsis, when mature dry seeds are hydrated, gel-like mucilage is extruded to
envelop the entire seed. Ruthenium red staining of Arabidopsis seeds reveals two different
mucilage layers, termed the nonadherent and the adherent mucilage layers (Western et al., 2000; Macquet et al., 2007a). The outer, nonadherent mucilage is loosely
attached and can be easily extracted by shaking seeds in water. Compositional and linkage
analyses suggest that this layer is almost exclusively composed of unbranched
rhamnogalacturonan I (RG-I) (>80% to 90%), with
small amounts of branched RG-I, arabinoxylan, and
high methylesterified homogalacturonan (HG). By
contrast, the inner, adherent mucilage layer is tightly attached to the seed and can only
be removed by strong acid or base treatment, or by enzymatic digestion (Macquet et al., 2007a; Huang et al., 2011; Walker et al.,
2011). As with the nonadherent layer, adherent mucilage is also mainly composed
of unbranched RG-I, but with small numbers of
arabinan and galactan ramifications (Penfield et al.,
2001; Willats et al., 2001; Dean et al., 2007; Macquet et al., 2007a, 2007b; Arsovski et al., 2009; Haughn and Western, 2012). There are also minor amounts of pectic
HG in the adherent mucilage, with high
methylesterified HG in the external domain compared
with the internal domain of the adherent layer (Willats
et al., 2001; Macquet et al., 2007a;
Rautengarten et al., 2008; Sullivan et al., 2011; Saez-Aguayo et al., 2013). In addition, the adherent mucilage
contains cellulose (Blake et al., 2006; Macquet et al., 2007a), which is entangled with RG-I and is thought to anchor the pectin-rich mucilage
onto seeds (Macquet et al., 2007a; Harpaz-Saad et al., 2011, 2012; Mendu et al., 2011;
Sullivan et al., 2011). As such, Arabidopsis
seed mucilage is considered to be a useful model for investigating the biosynthesis of cell
wall polysaccharides and how this process is regulated in vivo (Haughn and Western, 2012).Screening for altered seed coat mucilage has led to the identification of several genes
encoding enzymes that are involved in the biosynthesis or modification of mucilage
components. RHAMNOSE SYNTHASE2/MUCILAGE-MODIFIED4 (MUM4) is responsible for the synthesis
of UDP-l-Rha (Usadel et al., 2004; Western et al., 2004; Oka et al., 2007). The putative GALACTURONSYLTRANSFERASE11 can
potentially synthesize mucilage RG-I or HG pectin from UDP-d-GalUA (Caffall et al., 2009). GALACTURONSYLTRANSFERASE-LIKE5
appears to function in the regulation of the final size of the mucilage RG-I (Kong et al.,
2011, 2013). Mutant seeds defective in
these genes display reduced thickness of the extruded mucilage layer compared with
wild-type Arabidopsis seeds.RG-I deposited in the apoplast of seed coat
epidermal cells appears to be synthesized in a branched form that is subsequently modified
by enzymes in the apoplast. MUM2 encodes a β-galactosidase that
removes Gal residues from RG-I side chains (Dean et al., 2007; Macquet et al., 2007b). β-XYLOSIDASE1 encodes an
α-l-arabinfuranosidase that removes Ara residues from RG-I side chains (Arsovski et al., 2009). Disruptions of these genes lead to defective hydration
properties and affect the extrusion of mucilage. Furthermore, correct methylesterification
of mucilage HG is also required for mucilage
extrusion. HG is secreted into the wall in a high
methylesterified form that can then be enzymatically demethylesterified by pectin
methylesterases (PMEs; Bosch and Hepler, 2005). PECTIN METHYLESTERASE INHIBITOR6 (PMEI6)
inhibits PME activities (Saez-Aguayo et al., 2013). The subtilisin-like Ser protease (SBT1.7)
can activate other PME inhibitors, but not PMEI6
(Rautengarten et al., 2008; Saez-Aguayo et al., 2013). Disruption of either
PMEI6 or SBT1.7 results in the delay of mucilage
release.Although cellulose is present at low levels in adherent mucilage, it plays an important
adhesive role for the attachment of mucilage pectin to the seed coat epidermal cells. The
orientation and amount of pectin associated with the cellulose network is largely
determined by cellulose conformation properties (Macquet
et al., 2007a; Haughn and Western,
2012). Previous studies have demonstrated that CELLULOSE SYNTHASE A5 (CESA5) is
required for the production of seed mucilage cellulose and the adherent mucilage in the
cesa5 mutant can be easily extracted with water (Harpaz-Saad et al., 2011, 2012; Mendu et al., 2011; Sullivan et al., 2011).Despite all of these discoveries, large gaps remain in the current knowledge of the
biosynthesis and functions of mucilage polysaccharides in seed coats. In this study, we
show that CSLA2 is involved in the biosynthesis of mucilage glucomannan. Furthermore, we
show that CSLA2 functions in the maintenance of the normal structure of the adherent
mucilage layer through modifying the mucilage cellulose ultrastructure. 相似文献