The Lin28/let-7a/c-Myc pathway plays a role in non-muscle invasive bladder cancer

We investigate the role of the Lin28/let-7a/c-Myc pathway in non-muscle invasive bladder cancer (NMIBC). Using RT-PCR, western blot and immunohistochemistry techniques, the levels of pre-let-7a, let-7a, Lin28 and c-Myc RNA and/or proteins were determined in samples of normal bladder tissue and bladder cancer. Expression of pre-let-7a was found to be negatively correlated with the pathological grade of bladder cancer, while let-7a showed a positive correlation with bladder cancer pathological grade. Expression of Lin28 RNA and protein was not significantly different between normal bladder tissue and low-grade transitional cell carcinoma of bladder (TCC) but the expression levels in high-grade TCC were remarkably increased. Expression of c-Myc RNA and protein was significantly higher in bladder cancer samples in comparison to normal bladder tissue without correlation with cancer differentiation. Expression of all the above RNAs and proteins showed no significant difference in Ta and T1 stages. The Lin28/let-7a/c-Myc pathway plays an important role in NMIBC. In particular, expression levels of let-7a correlate with the degree of cancer differentiation but not cancer stage.     

Characterization and expression of gamma-interferon-inducible lysosomal thiol reductase (GILT) gene in rainbow trout (Oncorhynchus mykiss) with implications for GILT in innate immune response

The interferon-γ-inducible lysosomal thiol reductase (GILT) has been demonstrated to play an important role in the processing and presentation of MHC class II-restricted antigen (Ag) by catalyzing disulfide bond reduction. In this study, a rainbow trout cDNA (designated as rGILT) was cloned and identified from Oncorhynchus mykiss. The open reading frame of rGILT consists of 759 bases encoding a protein of 253 amino acids with an estimated molecular mass of 28.23 kDa and a theoretical isoelectric point of 4.94. The rGILT exhibited a characteristic GILT signature sequence CQHGX₂ECX₂NX₄C and CXXC motif. Phylogenetic analysis suggested that rGILT had been derived from a common ancestor with other GILT proteins. RT-PCR results showed that rGILT and rIFN-γ (rainbow trout IFN-γ) mRNA was expressed in a tissue-specific manner and obviously up-regulated in splenocytes and the cells from head kidney after induction with LPS. Recombinant rGILT fused with His6 tag was efficiently expressed in Escherichia coli BL21 (DE3) and purified by Ni-NTA affinity chromatography. Further study revealed that rGILT was capable of catalyzing the reduction of the interchain disulfide bonds from intact IgG. This study shows that rGILT may be involved in the immune response to bacteria challenge and maintain first line of innate immune defense at basal level in O. mykiss. It also provides the basis for investigating on the role of GILT using O. mykiss as an animal model for related studies.     

Expression, purification, and characterization of recombinant human soluble BAFF secreted from the yeast Pichia pastoris

The B lymphocyte stimulator (BAFF) is a novel member of the tumor necrosis factor (TNF) ligand family which is important in B lymphocyte maturation and survival. Herein, the cDNA coding for the extracellular domain of the BAFF (hsBAFF) has been cloned into the secreting expression organism Pichia pastoris. SDS-PAGE and Western blotting assays of culture broth from a methanol-induced expression strain demonstrated that recombinant hsBAFF, a 20.2 kDa glycosylated protein, was secreted into the culture medium. The recombinant protein was purified to greater than 95% using DEAE-Sepharose ion exchange and Superdex 75 size-exclusion chromatography steps. Finally, 102 mg of the protein was obtained in high purity from 1 L of the supernatant and its identity to hsBAFF was confirmed by NH(2)-terminal amino acid sequence analysis Bioactivity of the recombinant hsBAFF was confirmed by the ability of the protein to stimulate human B lymphocyte proliferation in vitro. Our results suggest that the P. pastoris expression system can be used to produce large quantities of fully functional hsBAFF for both research and industrial purpose.     

Production of glutamine synthetase in <Emphasis Type="Italic">Escherichia coli</Emphasis> using SUMO fusion partner and application to <Emphasis Type="SmallCaps">l</Emphasis>-glutamine synthesis

l-glutamine (Gln) is an important conditionally necessary amino acid in human body and potential demand in food or medicine industry is expected. High efficiency of l-Gln production by coupling genetic engineered bacterial glutamine synthetase (GS) with yeast alcoholic fermentation system has been developed. We report here first the application of small ubiquitin-related modifier (SUMO) fusion technology to the expression and purification of recombinant Bacillus subtilis GS. In order to obtain GS with high Gln-forming activity, safety and low cost for food and pharmaceutics industry, 0.1% (w/v) lactose was selected as inducer. The fusion protein was expressed in totally soluble form in E. coli, and expression was verified by SDS–PAGE and western blot analysis. The fusion protein was purified to 90% purity by nickel nitrilo-triacetic acid (Ni–NTA) resin chromatography with a yield of 625 mg per liter fermentation culture. After the SUMO/GS fusion protein was cleaved by the SUMO protease, the cleaved sample was reapplied to a Ni–NTA column. Finally, about 121 mg recombinant GS was obtained from 1 l fermentation culture with no less than 96% purity. The recombinant purified GS showed great transferase activity (23 U/mg), with 25 U recombinant GS in a 50 ml reaction system, a biosynthesis yield of 27.5 g/l l-Gln was detected by high pressure liquid chromatography (HPLC) or thin-layer chromatography. Thus, the application of SUMO technology to the expression and purification of GS potentially could be employed for the industrial production of l-Gln.     

Rongements sélectifs des os par les porcs-épics et autres rongeurs : cas de la grotte Tianyuan, un site avec des restes humains fossiles récemment découvert près de Zhoukoudian (Choukoutien)

The Tianyuan cave near Zhoukoudian is among the most special localities in North China for its many porcupine gnawing marks on the bones, as is often the case acknowledged only in South China. But porcupines did not gnaw all the bones, that is gnawing is selective. Skulls, mandibles, tooth roots and long bones are frequently gnawed. The short bones are almost free from gnawing. The selection indicates that, for porcupines, bone gnawing is not only a necessity for attrition of incisors, but also a process of extracting nutrients from the marrow. Additionally, the porcupine gnawing marks can also be employed to determine the provenance of the fossils that were discovered by the local people before the systematic excavation. Those bearing porcupine tooth marks only appear in the upper assemblage. The other significance of the gnawing marks is to infer the habitant of the cave. The bones from the human fossil bearing layer have few tooth marks, which may represent a period of human occupation of the cave. In the upper assemblage, the gnawing marks appear frequently, it may indicate that porcupine and other rodents lived in the cave during this time span.     

福建棕榈科原生植物资源分布与保护

棕榈科植物应用广泛,对其展开原生资源调查,有助于对其进行更为合理的保护与利用。该研究经过野外调查、收集整理有关资料,确定福建原生棕榈科资源为8属10种,其中鱼尾葵(Caryota maxima)为福建分布新记录。福建省棕榈科植物呈全省分散分布,南部种类更加丰富,以漳州市为最多(有8种),其次是龙岩、福州(各有4种)。棕榈、毛鳞省藤在福建省各市均有分布,属福建省广分布种;大叶蒲葵、鱼尾葵、刺葵、变色山槟榔、白藤仅见漳州分布,属福建省狭分布种。福建原生棕榈科植物大部分生长在亚热带常绿阔叶林中、林缘、山谷水沟旁等地,人为采伐利用或生境丧失是其导致濒危主要因素,就地保护、迁地保护、加强相关科学研究等是当前主要的保护措施。     

澳古茨藻传粉生物学和繁育系统的初步研究

澳古茨藻（ＮａｊａｓｏｇｕｒａｅｎｓｉｓＭｉｋｉ）是典型的水下水媒传粉植物。雄花在花粉释放前２—４ｈ花梗迅速伸长,突破膜质鞘状外被,并且向外弯曲,至花粉释放盛期几乎是水平状态,有利于释放后的花粉直接进入水流以求传播。花部组成与结构极为简化,花粉中富含淀粉粒,花粉落置柱头前常萌发出长的花粉管,形成宜为柱头捕获的花粉笺,表现出对水下水媒传粉的高度适应。有性繁殖十分发达,自交、异交和混交的结实率都在８５％以上;花粉／胚珠（Ｐ／Ｏ）为２６９０±３００,指示兼性自交的繁育系统。无性繁殖较弱,仅以易长不定根的植株片段形式存在,但仍对该种的扩散具有重要意义。作者对澳古茨藻的花生物学特征、传粉机制以及繁育系统进行了探讨,对澳古茨藻表现出的许多沉水植物所特有的特征特性：花被的简化、花粉外壁的简化作了解释,讨论了繁育系统中自交与异交的关系。     

许家窑遗址马科动物的死亡年龄

普氏野马(Equus przewalskii)和野驴(Equus hemionus)是许家窑遗址动物群中的优势属种。本文基于对这两种动物牙齿材料的测量与分析,确定了遗址中马科动物的死亡年龄,并对上、下文化层的死亡年龄分布进行了研究,以期探知古人类获取肉食资源的方式与特点。通过与马科动物在自然生存状态下以及死于不同原因(如疾病或营养衰竭、食肉动物猎杀、现代人类狩猎等)的年龄结构对比,结果表明:古人类在许家窑文化早期(下文化层)可能通过捡拾自然死亡的动物尸体、与食肉类动物抢夺猎物、主动狩猎等多种方式获取马科动物,而在许家窑文化晚期(上文化层)可能以主动狩猎作为获取马科动物的主要方式。此外,古人类在遗址的早期就可能已经具有捕获整个马科动物居群中任意年龄个体的能力,并能做出最优化判断,有选择地去捕猎脂肪和肉量较高的壮年动物群体。