贵州下寒武统牛蹄塘生物群中海绵新材料

描述了贵州下寒武统牛蹄塘生物群中海绵化石1新属(Zunyispongiagen.nov.),2新种(Zunyispongiatriangulariagen.etsp.nov.,Choiafanensis.sp.nov.),通过对其形态功能的分析和讨论证实了寒武纪早期海绵动物的骨骼是由细小骨针向粗大骨针演变,骨架结构从不稳定型向稳定型发展。     

New driver for lipid synthesis

Cholesterol regulates activation of sterol regulatory element-binding protein (SREBP) through a classic feedback loop. Walker et al. (2011) extend the regulatory inputs governing SREBP activity to include an independent loop modulated by phosphatidylcholine (PC) and cellular methylation capacity. These findings suggest a link between lipid synthesis and cellular pathways involved in methylation.     

A tale of too many centrosomes

Having the correct number of centrosomes is crucial for proper chromosome segregation during cell division and for the prevention of aneuploidy, a hallmark of many cancer cells. Several recent studies (Basto et al., 2008; Kwon et al., 2008; Yang et al., 2008) reveal the importance of mechanisms that protect against the consequences of harboring too many centrosomes.     

灵芝三萜类化合物抗癌作用机制的研究进展

<正>INTRODUCTION Ganoderma lucidum(Fr.)P.Karst.,a species of higher fungus called"Lingzhi"in Chinaor"Reishi"and"Mannendake"in Japan,has been used in the traditional Chinese medicine(TCM)for prevention and treatment     

中国海相早三叠世弓鲛鱼类(软骨鱼类)的首次报道——华南二叠系一三叠系界线上下鱼类序列研究之一

广西田东县作登下三叠统罗楼组产出弓鲛鱼类作登弓鲛Hybodus zuodengensis(Yang et al.)、乐氏弓鲛H.yohi(Yang et al.)和田东多尖齿鱼(新种)Polyacrodus tiandongensis sp.nov.,其中前二种化石以前曾被作为牙形类报道.这是弓鲛鱼类在中国海相早三叠世的首次报道.另外,本组还产出属种未定的硬骨鱼类化石(Osteichthyes gen.et sp.indet.).建立了我国海相早三叠世第一个鱼类带化石,作登弓鲛-乐氏弓鲛组合带(Hybodus zuodengensisH.yhoi AZ);伴生的有Neospathodushomeri-N.triangularis牙形类带化石,该带化石延续的时限为奥伦尼克阶(Olenekian)司帕斯期(Spathian)早期.     

中国海相早三叠世弓鲛鱼类(软骨鱼类)的首次报道——华南二叠系—三叠系界线上下鱼类序列研究之一

广西田东县作登下三叠统罗楼组产出弓鲛鱼类 :作登弓鲛Hyboduszuodengensis(Yangetal.)、乐氏弓鲛H .yohi (Yangetal.)和田东多尖齿鱼 (新种 )Polyacrodustiandongensissp .nov .,其中前二种化石以前曾被作为牙形类报道。这是弓鲛鱼类在中国海相早三叠世的首次报道。另外 ,本组还产出属种未定的硬骨鱼类化石 (Osteichthyesgen .etsp .indet.)。建立了我国海相早三叠世第一个鱼类带化石 ,作登弓鲛—乐氏弓鲛组合带 (Hyboduszuodengensis H .yohiAZ) ;伴生的有Neospathodushomeri N .triangularis牙形类带化石 ,该带化石延续的时限为奥伦尼克阶 (Olenekian)司帕斯期 (Spathian)早期。     

柴达木盆地西部红柳泉地区晚侏罗世介形类动物群及其古环境意义

在柴达木盆地红柳泉地区红探2井红水沟组中识别出介形类化石3属9种(含2个未定种):Cetacella qaidamensis Li et Yang, 1983、Djungarica tracta Li et Yang, 1983、Djungarica sp.、Alicenula incurva (Bate, 1967)、?A.longicylindrica (Qi, 1985)、A. paramagna (Li et Yang, 1983)、A. maanshanensis (Hou et al., 2002)、A. jinhuaensis (Li,1984)、Alicenula sp.。通过介形类化石生物地层对比,明确红水沟组的沉积时代为晚侏罗世。红水沟组介形类动物群指示晚侏罗世柴达木地区发育淡水湖泊、河流以及季节性的小水塘。     

Roles of Arabidopsis PARC6 in Coordination of the Chloroplast Division Complex and Negative Regulation of FtsZ Assembly

Chloroplast division is driven by the simultaneous constriction of the inner FtsZ ring (Z ring) and the outer DRP5B ring. The assembly and constriction of these rings in Arabidopsis (Arabidopsis thaliana) are coordinated partly through the inner envelope membrane protein ACCUMULATION AND REPLICATION OF CHLOROPLASTS6 (ARC6). Previously, we showed that PARC6 (PARALOG OF ARC6), also in the inner envelope membrane, negatively regulates FtsZ assembly and acts downstream of ARC6 to position the outer envelope membrane protein PLASTID DIVISION1 (PDV1), which functions together with its paralog PDV2 to recruit DYNAMIN-RELATED PROTEIN 5B (DRP5B) from a cytosolic pool to the outer envelope membrane. However, whether PARC6, like ARC6, also functions in coordination of the chloroplast division contractile complexes was unknown. Here, we report a detailed topological analysis of Arabidopsis PARC6, which shows that PARC6 has a single transmembrane domain and a topology resembling that of ARC6. The newly identified stromal region of PARC6 interacts not only with ARC3, a direct inhibitor of Z-ring assembly, but also with the Z-ring protein FtsZ2. Overexpression of PARC6 inhibits FtsZ assembly in Arabidopsis but not in a heterologous yeast system (Schizosaccharomyces pombe), suggesting that the negative regulation of FtsZ assembly by PARC6 is a consequence of its interaction with ARC3. A conserved carboxyl-terminal peptide in FtsZ2 mediates FtsZ2 interaction with both PARC6 and ARC6. Consistent with its role in the positioning of PDV1, the intermembrane space regions of PARC6 and PDV1 interact. These findings provide new insights into the functions of PARC6 and suggest that PARC6 coordinates the inner Z ring and outer DRP5B ring through interaction with FtsZ2 and PDV1 during chloroplast division.Chloroplasts evolved from an ancient cyanobacterium through endosymbiosis (Gould et al., 2008; Keeling, 2013). Like their prokaryotic relatives, chloroplasts replicate by binary fission, which is driven by a dynamic macromolecular complex located at the middle of the organelle (Falconet, 2011; Miyagishima et al., 2011; Osteryoung and Pyke, 2014). The major contractile components of the division complex include the FtsZ ring (Z ring), which assembles on the stromal surface of the inner envelope membrane (IEM; McAndrew et al., 2001; Vitha et al., 2001), and the DYNAMIN-RELATED PROTEIN 5B (DRP5B; also called ACCUMULATION AND REPLICATION OF CHLOROPLASTS5 [ARC5]) ring, which assembles on the cytosolic surface of the outer envelope membrane (OEM; Gao et al., 2003; Miyagishima et al., 2003; Yoshida et al., 2006). In green algae and land plants, the Z ring is composed of the tubulin-like, heteropolymer-forming proteins FtsZ1 and FtsZ2, which are both required for normal Z-ring function (Schmitz et al., 2009; TerBush and Osteryoung, 2012). DRP5B is a member of the dynamin family of membrane fission proteins, which polymerize into collar-like structures to mediate a variety of membrane fission processes in eukaryotes (Morlot and Roux, 2013). The Z ring and DRP5B ring function together to drive the simultaneous constriction of the IEM and OEM during chloroplast division.The assembly and constriction of the inner Z ring and outer DRP5B ring are coordinated across the two membranes by the activities of midplastid-localized envelope membrane proteins whose functions have been studied in Arabidopsis (Arabidopsis thaliana). ARC6 (Pyke et al., 1994) is a bitopic IEM protein of cyanobacterial origin that is conserved throughout green-lineage chloroplasts (Koksharova and Wolk, 2002; Vitha et al., 2003; Osteryoung and Pyke, 2014). Its N-terminal region extends into the stroma, where it interacts directly and specifically with FtsZ2 (Maple et al., 2005). As FtsZ1 and FtsZ2 are soluble (McAndrew et al., 2001), this interaction probably serves both to tether the Z ring to the IEM and to promote FtsZ polymerization at the division site (Vitha et al., 2003). The C-terminal region of ARC6 protrudes into the intermembrane space (IMS) and interacts with the IMS region of the plant-specific bitopic OEM protein PLASTID DIVISION2 (PDV2). ARC6-PDV2 interaction is required for the localization of PDV2 to the midplastid (Glynn et al., 2008). PDV2 and its paralog PDV1, also in the OEM, in turn recruit DRP5B from a cytosolic pool to the OEM (Miyagishima et al., 2006), probably through direct interaction with their cytosolic regions (Holtsmark et al., 2013). Thus, interactions between FtsZ2 and ARC6 in the stroma, ARC6 and PDV2 in the IMS, and PDV2 (and PDV1) and DRP5B in the cytosol connect and coordinate the FtsZ and DRPB5B rings across the IEM and OEM.Previously, we showed that, despite the fact that an interaction between the IMS regions of ARC6 and PDV1 could not be detected, ARC6 was nevertheless required for the equatorial localization of PDV1 as well as PDV2, suggesting the existence of a factor that acted downstream of ARC6 to position PDV1 (Glynn et al., 2008). This downstream factor was subsequently shown to be the nucleus-encoded chloroplast division protein PARALOG OF ARC6 (PARC6; Glynn et al., 2009), also called CDP1 (Zhang et al., 2009) and ARC6H (Ottesen et al., 2010). parc6 mutants exhibited mislocalization of PDV1 but not PDV2, demonstrating a specific role for PARC6 in PDV1 positioning. PARC6 is restricted to vascular plants, suggesting that it arose by the duplication and divergence of ARC6 following separation of the nonvascular and vascular lineages. As suggested by its name, PARC6 shares significant sequence similarity with ARC6 and is similarly imported to the chloroplast by a cleavable N-terminal transit peptide and localized in the IEM. However, whereas ARC6 has a single transmembrane domain (TMD), PARC6 is predicted to bear two, and while a portion of its N terminus was clearly shown to reside in the stroma, its full topology has not been established (Glynn et al., 2009). Furthermore, genetic analysis suggested that, unlike ARC6, which positively regulates FtsZ assembly (Vitha et al., 2003), PARC6 functions partly as a negative regulator of FtsZ assembly. Interaction assays provided evidence that this negative regulation may be mediated by interaction of the N terminus of PARC6 with the stromal division protein ARC3 (Pyke et al., 1994; Shimada et al., 2004; Maple et al., 2007), a Z-ring positioning factor recently shown to inhibit Z-ring assembly and/or promote FtsZ filament and Z-ring destabilization (TerBush and Osteryoung, 2012; Zhang et al., 2013; Johnson et al., 2015). Although the interaction of PARC6 with FtsZ was not detected previously, the significance of this finding has remained uncertain in the absence of definitive data on PARC6 topology (Glynn et al., 2009).Here, we report a detailed topological analysis of Arabidopsis PARC6, investigate its interactions with other division factors, and assess the effect of PARC6 on chloroplast FtsZ assembly. Our findings provide evidence that the negative effect of PARC6 on Z-ring assembly results from its interaction with ARC3 and reveal a role for PARC6 in coordinating the inner Z ring and outer DRP5B ring partially analogous to the role of ARC6.     

Revision on Cephalostachyum Munro (Poaceae: Bambusoideae) in China

Species of Cephalostachyum Munro (Poaceae: Bambusoideae) from China are distributed in Yunnan and Tibet, mainly in Yunnan. In this paper, we discussed species of Cephalostachyum and compiled a key to species from China, based on recent studies on micromorphological characters of leaf epidermis and molecular phylogenetics of paleotropical woody bamboos. There is a total of seven species of Cephalostachyum distributed in China, all in Yunnan: Cchinense (Rendle) DZ. Li et HQ. Yang, Cfuchsianum Gamble et Hook. f., Cmannii (Gamble) Stapleton et DZ. Li, Cpallidum Munro, Cpingbianense (Hsueh et YM. Yang ex Yi et al.) DZ. Li et HQ. Yang, Csanguineum (WP. Zhang) DZ. Li et HQ. Yang and Cscandens Bor. Leptocanna Chia et HL. Fung and Cvirulentum YM Yang et F. Du are synonyms of Cephalostachyum Munro and Cfuchsianum Gamble et Hook. f. respectively. On the other hand, Cpergracile Munro and Cvirgatum (Munro) Kurz are morphologically closer to Schizostachyum Nees than to Cephalostachyum, and they should be treated as members of Schizostachyum. This paper is of significance to a worldwide revision of Cephalostachyum.     

Releasing the brake on presynaptic development: Cdc20-APC triggers NeuroD2 degradation to drive presynaptic differentiation

Comment on: Yang Y, et al. Science 2009; 326:575-8.     

甘肃西部花海子盆地第四纪介形类Subulacypris

本文记述了花海子盆地第四纪介形类动物群中占绝对优势的Subulacypris,共7个种,其中新种4个。依据该属种产出层特性及其在介形类动物群中的分布特征推测,适于这些种的生活环境应属严寒气候条件下的冰水河流,化石壳体微量元素分析结果提供的环境信息与这一推测相吻合。     

Transmitter time: synaptic plasticity and metabolic memory in the hypothalamus

Hunger elicits feeding behavior by activating Agouti-related peptide (AgRP) neurons. Two recent studies show how fasting, or the hunger hormone ghrelin, promote excitatory glutamate release onto AgRP neurons (Yang et?al., 2011) and increase postsynaptic glutamate receptor-mediated drive (Liu et?al., 2012).     

Protaitzehoia Yang三叶虫分类位置的再研究-答“也论Protaitzehoia Yang三叶虫的分类位置”．．．

文章从三叶虫的头尾搭配问题的讨论对"也论Protaitzehoia Yang三叶虫的分类位置"一文中置于原太子河虫属的某些尾部的可靠性提出了质疑,认为插图2中的尾(K),由于缺少宽而下凹的尾边缘,应属于Stephanocare Monke,1903一属的尾部;插图2中的尾(L)的归属尚难定论.将原太子河虫属的头盖、活动颊、尾部、唇瓣与Cheilocephalus Berkey,1898属的头盖、活动颊、尾部、唇瓣对比后,认为原太子河虫属应归属Cheilocephalidae Shaw,1956.     

New functions for the Snail family of transcription factors: Two-faced proteins

Comment on: Yang D, et al. Cell Cycle 2010; 9:2789-802.     

A novel neuronal differentiation mechanism in which Slug and Escargot are major players

Comment on: Yang D, et al. Cell Cycle 2010; 9:9:2789-802.     

华南浅海相泥盆系吉维特阶和弗拉阶四射珊瑚组合特征

中泥盆世吉维特晚期(更精确的说是在中吉维特期末)发生的生物更替事件使大量的头贝、全部的泡沫珊瑚亚目以及大多数的绳珊瑚科和内板珊瑚科惨遭灭绝。晚泥盆世弗拉期出现了许多新生分子,诸如Micto-phyllum,Wapitiphyllum,Pseudozaphrentis,Peneckiella等。根据珊瑚的不同组合特征可以鉴别出它们的地质时代。华南自上而下可划分出4个四射珊瑚组合,分别为上泥盆统弗拉阶(Frasnian):4)Disphyllum-Wapitiphyl-lum组合(牙形类gigas或rhenana带和hassi-jamieae带),3)Mictophyllum-Pseudozaphrentis组合(牙形类asymmetricus带);中泥盆统吉维特阶(Givetian):2)Endophyllum-Sunophyllum组合(牙形类varcus带的中部和下部之上段),1)Stringophyllum-Paramixogonaria组合(牙形类hemiansatus带-varcus带最下部)。     

Cytochrome P450 reductase (POR)as a ferroptosis fuel

Oxygen,iron,and polyunsaturated fatty acids (PUFAs;fatty acids containing more than one double bond) are all bene-ficial to our cellular lives.Incorporation of these components into cellular processes,however,comes at a cost:the bis-allylic structure of PUFAs and the enrichment of cellular environments with iron and oxygen render PUFA-containing phospholipids (PUFA-PLs) particularly susceptible to per-oxidation (Yang and Stockwell,2016).Accumulation of lethal amounts of lipid peroxides in cell membranes leads to a form of cell death known as ferroptosis (Dixon et al.,2012;Stockwell et al.,2017;Stockwell and Jiang,2020).Conse-quently,cells are equipped with strong antioxidant defense systems that constantly dissipate toxic lipid peroxides gen-erated in cellular membranes,thereby maintaining cell via-bility and homeostasis (Zheng and Conrad,2020).The most powerful anti-ferroptosis defense system is believed to be mediated by glutathione peroxidase 4 (GPX4),a glutathione peroxidase that uses glutathione as its cofactor to reduce lipid hydroperoxides to non-toxic lipid alcohols (Fig.1)(Zheng and Conrad,2020).A variety of ferroptosis inducers(FINs) act to inactivate GPX4 or deplete glutathione,causing an imbalance between the production and detoxification of lipid peroxides that subsequently induces ferroptotic cell death (Yang et al.,2014).Genetic ablation of GPX4 can have the same effect (Friedmann Angeli et al.,2014).