蜜蜂级型分化机理

蜜蜂是整个大自然生态系统中不可或缺的一部分,能有效地为多种植物和农作物授粉。蜜蜂是典型的真社会性昆虫,其生殖劳动分工现象有重要进化意义。而级型分化是导致劳动分工的一个重要因素,蜜蜂级型分化现象的机理研究已成为目前重要的研究热点之一。本文对近年来蜜蜂级型分化机理方面的研究进展进行了综述。国内外很多学者从营养、激素、基因表达、蛋白质和表观遗传等方面对蜜蜂级型分化机理进行了研究。蜂王浆中富含的57 kDa、蜂王幼虫期充足的食物量以及蜂王幼虫期高滴度的保幼激素(JH)和蜕皮激素(MA)等都可促进蜂王卵巢的发育以及诱导蜂王表型产生;而工蜂浆中富含的双香豆酸可诱使工蜂表型的产生。近年研究表明,表皮生长因子受体(Egfr)、胰岛素受体底物基因(Irs)、雷帕霉素基因(Tor)和甲基转移酶3(Dnmt3)等基因均可影响蜂王和工蜂的分化;蛋白质表达谱分析表明,不同时间点的蜂王幼虫和工蜂幼虫表达的差异蛋白质很多;表观遗传分析表明,DNA甲基化、microRNAs以及组蛋白乙酰化均是导致蜂王和工蜂级型分化的因素。此外,发育空间和蜂王浆均可通过调控基因的DNA甲基化水平影响蜜蜂幼虫的级型分化。     

蜜蜂蜂王与工蜂级型分化研究进展

蜜蜂ApismekiferaL .是典型的社会性昆虫 ,蜂王和工蜂都是由受精卵发育而来的二倍体成蜂 ,但是在形态、生理、行为等方面有明显的差异 ,属于不同的级型。蜂王和工蜂的级型分化的关键时期发生在幼虫的 4龄末至 5龄止。分化是由分化基因调控的 ,幼虫期食物的质和量是分化的外部决定因子。JH对两级型中卵巢的分化有非常重要的调控作用。蜜蜂脑或其它组织中可能有分泌调控CA的咽侧体调节激素 ,它们通过对CA中JH的合成和分泌的调控而参与了分化的调控。章鱼胺等生物胺也参与了分化调控过程。     

LncRNA在蜜蜂级型分化中的功能研究

蜜蜂的级型分化被证实是由蜂王浆中的Royalactin决定,工蜂和蜂王幼虫在级型分化时编码基因的表达差异也被广泛研究.我们发现,在蜜蜂幼虫的级型分化过程中,lncRNA也有着显著的表达差异,因此认为,lncRNA也参与了蜜蜂的级型分化过程.进一步的分析显示,lncRNA可能通过影响上下游基因的转录和功能执行的方式,在蜜蜂早期发育的多细胞组织发育、神经系统发育和转录调控的过程中起到重要的调控作用.     

蜜蜂级型分化机理

蜜蜂Apis spp.能有效地为多种植物及农作物授粉, 具有重要的经济和生态价值; 蜜蜂作为高度真社会性昆虫, 已成为社会生物学研究的模式生物。社会性昆虫的生殖劳动分工具有重要的进化意义, 而级型分化是形成生殖劳动分工的基础。近年来, 关于蜜蜂级型分化的研究已取得诸多重要成果, 其机理也得到了较为深入的阐释。营养差异引发蜜蜂幼虫的级型分化。蜂王浆中的主要蛋白组分之一--Royalactin是诱导蜂王发育的关键营养因子, 而脂肪体细胞的表皮生长因子受体介导了Royalactin的这种蜂王诱导作用。DNA甲基化是重要的表观遗传机制之一, 且与个体发育和疾病发生紧密相关, 近来的研究表明DNA甲基化在蜜蜂级型分化过程中发挥重要的调控作用。此外, 越来越多的研究进一步深化了人们对内分泌系统调节级型分化作用的认识。本文从关键营养因子调控、 表观遗传调控和内分泌调节3方面综述蜜蜂级型分化的机理, 并对未来的研究提出可能的方向。     

蜜蜂级型分化相关生理因子研究进展

蜜蜂Apis melliferaL.是典型的社会性昆虫,蜂群内蜂王和工蜂的级型分化现象吸引了众多研究者的高度关注。蜜蜂级型分化是一个极为复杂的生长发育调节过程,许多重要生理因子参与其中,包括保幼激素、蜕皮激素、胰岛素/胰岛素类似物信号通路等。本文概述了蜜蜂级型分化相关生理因子研究进展:保幼激素决定着蜜蜂级型发育的轨迹并能阻止卵巢发育过程中细胞的程序性死亡;蜕皮激素协同保幼激素发挥调节作用;蜜蜂蜂王与工蜂的躯体大小及相关器官大小的级型特异性差异与胰岛素/胰岛素类似物信号通路密切相关。此外,本文还介绍了蜜蜂级型分化模型,该模型系统描述了上述各生理因子对级型分化的综合作用。     

本期重点推介

正蜜蜂Apis spp.是具有级型分化的社会性昆虫。揭示其级型分化及调控机理,对认识社会性昆虫的演化形成机制、不同级型的发育和维持机理以及对其更好地加以应用均有重要的参考价值。已有研究表明,蜂王浆的主要蛋白成分———王浆主蛋白(major royal jelly proteins,MRJPs)在蜜蜂的级型分化中具有重要的功能。mrjp8是mrjps家族中较晚发现的一个成员。为了进一步明确mrjp8基因表达与蜜蜂级型分化的关系,福建农林大学蜂学学院李江红等对西方蜜蜂Apis mellifera不同发育龄期工蜂体内,以及成年工蜂、新出房蜂王和雄蜂不同组织中的mrjp8表达水平进行了检测,发现     

熊蜂级型分化研究进展

熊蜂是众多野生植物及农作物的有效授粉昆虫,具有重要的经济和生态价值。熊蜂复杂的生长发育过程及社会性使其成为社会生物学研究的最佳模式生物之一。社会性昆虫的生殖劳动分工具有重要的进化意义,而级型分化是形成生殖劳动分工的基础。蜜蜂级型分化的研究已取得诸多重要成果,其机理也得到了较为深入的阐释,而熊蜂的社会性研究尚未形成系统,与蜜蜂研究相差甚远。近来的研究表明,饲喂频率或者饲喂总量的差异能够引起熊蜂级型分化的发生。保幼激素和蜕皮激素与熊蜂幼虫的发育紧密联系,在熊蜂级型分化的过程中发挥重要作用。一些参与蜜蜂级型分化的基因,在熊蜂级型间也存在差异表达。此外,群体间的相互作用以及蜂王和工蜂间的竞争也是促进熊蜂级型分化发生的重要因素。本文从营养、激素调控、群体发展及相互作用等方面综述熊蜂级型分化机制,并对未来的研究提出可能方向。     

意蜂SOD和POD同工酶在工蜂、雄蜂和蜂王之间的比较

用聚丙烯酰胺凝胶电泳的方法,以意大利蜜蜂工蜂、雄蜂和蜂王以及两种不同大小幼虫之间的超氧化物歧化酶(SOD)和过氧化物酶(POD)同工酶分别作了比较。结果表明,这2种同工酶在意蜂幼虫阶段与成体阶段均有明显差异;意蜂工蜂、雄蜂和蜂王都有着不同的同工酶谱型。说明意蜂同工酶在种内的表达受到发育程度、进食质量、分化方向等因素的影响。     

蜜蜂群内生殖分工体系的形成及其维持

本文对蜜蜂群内生殖分工体系的形成及其维持机制进行综述。蜜蜂群体具有完善的劳动分工(包括生殖分工)体系,蜂王垄断生殖权力,而工蜂生殖器官发育不完全,在蜂王信息素和幼虫信息素的作用下产卵受到抑制。蜂王的多雄交配机制降低了群内个体间的亲缘关系,但也促进了工蜂间相互监督机制的形成。工蜂间的相互监督,结合蜂王和幼虫信息素对工蜂卵巢发育的影响,解决了蜂王与工蜂、工蜂与工蜂间的生殖利益冲突,保障了蜂群内的生殖分工体系,提高了群体效率,维护了蜂群的真社会性。     

东西方蜜蜂亲缘行为关系研究取得新进展

东方蜜蜂和西方蜜蜂是2个不同的种,二者的亲缘关系很近,但是二者的蜂王和幼虫均具有不同的遗传物质和气味信息素,蜜蜂的气味信息素对蜜蜂的社会行为和行为方式起到非常重要的作用。建立东方蜜蜂和西方蜜蜂的混合饲养蜂群,为研究东方蜜蜂和西方蜜蜂这2个近缘物种间的相互关系提供了一个很好的模式。近日,中国科学院西双版纳热带植物园协同进化组的高级访问学者谭垦教授等,通过测试和分析东方蜜蜂蜂王和西方蜜蜂蜂王的蜂王信息素主要成分的组成和差异,研究蜂王在混合饲养蜂群内对异种工蜂卵巢发育的抑制作用,并探讨了当混合蜂群失去蜂王后,2种工蜂对异种蜜蜂卵和幼虫气味的识别和反应机制。     

Role for dopamine in malonate-induced damage in vivo in striatum and in vitro in mesencephalic cultures

Defects in mitochondrial energy metabolism have been implicated in the pathology of several neurodegenerative disorders. In addition, the reactive metabolites generated from the metabolism and oxidation of the neurotransmitter dopamine (DA) are thought to contribute to the damage to neurons of the basal ganglia. We have previously demonstrated that infusions of the metabolic inhibitor malonate into the striata of mice or rats produce degeneration of DA nerve terminals. In the present studies, we demonstrate that an intrastriatal infusion of malonate induces a substantial increase in DA efflux in awake, behaving mice as measured by in vivo microdialysis. Furthermore, pretreatment of mice with tetrabenazine (TBZ) or the TBZ analogue Ro 4-1284 (Ro-4), compounds that reversibly inhibit the vesicular storage of DA, attenuates the malonate-induced DA efflux as well as the damage to DA nerve terminals. Consistent with these findings, the damage to both DA and GABA neurons in mesencephalic cultures by malonate exposure was attenuated by pretreatment with TBZ or Ro-4. Treatment with these compounds did not affect the formation of free radicals or the inhibition of oxidative phosphorylation resulting from malonate exposure alone. Our data suggest that DA plays an important role in the neurotoxicity produced by malonate. These findings provide direct evidence that inhibition of succinate dehydrogenase causes an increase in extracellular DA levels and indicate that bioenergetic defects may contribute to the pathogenesis of chronic neurodegenerative diseases through a mechanism involving DA.     

Scurvy in capybaras bred in captivity in Argentine

In order to determine if the absence of vitamin C in the diet of capybaras (Hydrochoerus hydrochaeris) causes scurvy, a group of seven young individuals were fed food pellets without ascorbic acid, while another group of eight individuals received the same food with 1 g of ascorbic acid per animal per day. Animals in the first group developed signs of scurvy-like gingivitis, breaking of the incisors and death of one animal. Clinical signs appeared between 25 and 104 days from the beginning of the trial in all individuals. Growth rates of individuals deprived of vitamin C was considerably less than those observed in the control group. Deficiency of ascorbic acid had a severe effect on reproduction of another population of captive capybaras. We found that the decrease in ascorbic acid content in the diet affected pregnancy, especially during the first stages. The results obtained suggest that it is necessary to supply a suitable quantity of vitamin C in the diet of this species in captivity.     

Changes in lactate dehydrogenase activity in chicken tissues in hyperthyreosis in ontogenesis

The lactate dehydrogenase activity in reactions of lactate oxidation and synthesis was studied in subfractions of the chicken brain, heart and liver at the embryonal, early postembryonal and adult stages of development after thyroxine administration. It has been shown that during embryogenesis thyroxine predominantly enhanced the rate of lactate oxidation in the mitochondrial tissues. A marked increase in the lactate synthesis was found in cytoplasm of the adult chicken tissues. Specificity of enzyme activity alterations was detected in the chicken brain during ontogenesis after thyroxine administration.     

SSTR5 ablation in islet results in alterations in glucose homeostasis in mice

Somatostatin (SST) peptide is a potent inhibitor of insulin secretion and its effect is mediated via somatostatin receptor 5 (SSTR5) in the endocrine pancreas. To investigate the consequences of gene ablation of SSTR5 in the mouse pancreas, we have generated a mouse model in which the SSTR5 gene was specifically knocked down in the pancreatic beta cells (betaSSTR5Kd) using the Cre-lox system. Immunohistochemistry analysis showed that SSTR5 gene expression was absent in beta cells at three months of age. At the time of gene ablation, betaSSTR5Kd mice demonstrated glucose intolerance with lack of insulin response and significantly reduced serum insulin levels. Insulin tolerance test demonstrated a significant increase of insulin clearance in vivo at the same age. In vitro studies demonstrated an absence of response to SST-28 stimulation in the betaSSTR5Kd mouse islet, which was associated with a significantly reduced SST expression level in betaSSTR5Kd mice pancreata. In addition, betaSSTR5Kd mice had significantly reduced serum glucose levels and increased serum insulin levels at 12 months of age. Glucose tolerance test at an older age also indicated a persistently higher insulin level in betaSSTR5Kd mice. Further studies of betaSSTR5Kd mice had revealed elevated serum C-peptide levels at both 3 and 12 months of age, suggesting that these mice are capable of producing and releasing insulin to the periphery. These results support the hypothesis that SSTR5 plays a pivotal role in the regulation of insulin secretion in the mouse pancreas.