Neoplastic progression of rat tracheal epithelial cells is associated with a reduction in the number of growth factors required for clonal proliferation in culture

Summary Factors regulating the proliferation of normal, preneoplastic, and neoplastic rat tracheal epithelial (RTE) cells were investigated to identify changes taking place during the progression of RTE cells to neoplasia. Normal RTE cells exhibit clonal proliferation in a serum-free medium containing pituitary extract, serum albumin, cholera toxin, epidermal growth factor, hydrocortisone, and insulin. All combinations of these six factors were examined for their abilities to support clonal proliferation of normal, preneoplastic, and neoplastic RTE cells. In general, preneoplastic RTE cells required fewer factors for proliferation than normal RTE cells, and neoplastic cells required fewer factors than preneoplastic cells. A common pattern of reductions has been identified in the growth factors required for the clonal proliferation of preneoplastic vs. normal RTE cells and for neoplastic vs. preneoplastic and normal RTE cells. Normal RTE cells exhibit clonal proliferation in a serum-free medium supplemented with a minimum of six factors: bovine serum albumin, bovine pituitary extract, cholera toxin, epidermal growth factor, hydrocortisone, and insulin. Preneoplastic RTE cells exhibit clonal proliferation in a serum-free medium supplemented with four factors: bovine serum albumin, bovine pituitary extract, hydrocortisone, and insulin. Finally, neoplastic RTE cells exhibit clonal proliferation in a serum-free medium supplemented with two factors: bovine serum albumin and bovine pituitary extract. These results suggest that the progression of RTE cells to neoplasia is associated with a series of changes in regulatory pathways that control cell proliferation.     

Selected factors limiting the microbial degradation of recalcitrant compounds

Summary The focus of this review is to examine some of the reasons biodegradation may not take place in the environment even though its occurrence in the laboratory has been demonstrated. Some approaches for dealing with chemical persistence will be discussed. In addition, the potential of bioremediation as an in situ clean-up technology will be considered.     

The distribution of coastal fish eDNA sequences in the Anthropocene

Aim

Coastal fishes have a fundamental role in marine ecosystem functioning and contributions to people, but face increasing threats due to climate change, habitat degradation and overexploitation. The extent to which human pressures are impacting coastal fish biodiversity in comparison with geographic and environmental factors at large spatial scale is still under scrutiny. Here, we took advantage of environmental DNA (eDNA) metabarcoding to investigate the relationship between fish biodiversity, including taxonomic and genetic components, and environmental but also socio-economic factors.

Location

Tropical, temperate and polar coastal areas.

Time period

Present day.

Major taxa studied

Marine fishes.

Methods

We analysed fish eDNA in 263 stations (samples) in 68 sites distributed across polar, temperate and tropical regions. We modelled the effect of environmental, geographic and socio-economic factors on α- and β-diversity. We then computed the partial effect of each factor on several fish biodiversity components using taxonomic molecular units (MOTU) and genetic sequences. We also investigated the relationship between fish genetic α- and β-diversity measured from our barcodes, and phylogenetic but also functional diversity.

Results

We show that fish eDNA MOTU and sequence α- and β-diversity have the strongest correlation with environmental factors on coastal ecosystems worldwide. However, our models also reveal a negative correlation between biodiversity and human dependence on marine ecosystems. In areas with high dependence, diversity of all fish, cryptobenthic fish and large fish MOTUs declined steeply. Finally, we show that a sequence diversity index, accounting for genetic distance between pairs of MOTUs, within and between communities, is a reliable proxy of phylogenetic and functional diversity.

Main conclusions

Together, our results demonstrate that short eDNA sequences can be used to assess climate and direct human impacts on marine biodiversity at large scale in the Anthropocene and can further be extended to investigate biodiversity in its phylogenetic and functional dimensions.     

Differential induction of regulatory genes during mesoderm formation in Xenopus laevis embryos

Mesoderm development in Xenopus laevis depends on inductive cell interactions mediated by diffusible molecules. The mesoderm inducer activin is capable of redirecting the development of animal explants both morphologically and biochemically. We have studied the induction of four regulatory genes, Mix. 1, goosecoid (gsc), Xlim-1 and Xbra in such explants by activin, and the influence of other factors on this induction. Activin induction of gsc is strongly enhanced by dorsalization of the embryo by LiCl, while expression of the other genes is only slightly enhanced. The protein synthesis inhibitor cycloheximide (CHX) inhibits the activin-dependent induction of Xbra partially, while induction of Mix. 1 and Xlim- 1 is essentially unaffected. In contrast, gsc shows strong superinduction in the presence of activin and CHX, and can be induced in animal explants by CHX alone. Induction and superinduction by CHX have previously been observed for immediate early genes in a variety of systems, notably for the activation of c-fos expression by serum stimulation, but have not been reported in early amphibian embryos. © 1993Wiley-Liss, Inc.     

尖峰岭热带天然林不同土层细菌群落多样性和组成的海拔变异规律

土壤微生物群落结构沿海拔梯度的变异是微生物生物地理学分异和群落空间分布的重要内容,然而,热带森林土壤微生物多样性及其群落特征的海拔模式尚不明确。研究海南省尖峰岭自然保护区0—20cm和20—40cm土壤细菌多样性和群落组成沿海拔梯度(400—1410m)的变化及其与环境因子的关系。结果表明：在0—20cm土壤微生物生物量碳、生物量氮和生物量磷随海拔升高(峰顶降低)而增加,20—40cm土壤微生物生物量碳、生物量氮和生物量磷随海拔升高呈先升高后降低趋势;整体上,变形菌门、放线菌门、酸杆菌门、拟杆菌门、厚壁菌门在0—20cm中占优势,丰度总和占该层细菌总量的88.17%;变形菌门、放线菌门、酸杆菌门、厚壁菌门、绿弯菌门在20—40cm中占优势,丰度总和占该层细菌总量的90.82%;随海拔增加,0—20cm细菌多样性线性减少,20—40cm细菌多样性变化不显著;沿海拔梯度,0—20cm细菌群落组成可分为低(409—1018m),中(1018—1357m)和高(1410m)三个海拔聚集群落,20—40cm细菌群落组成随海拔无显著性变化;两土层细菌多样性与土壤pH显著正相关,土壤细菌群落组成在0...     

2001—2019年中国自然保护区生态环境质量时空变化特征及其驱动力

自然保护区对维护生物多样性,改善生态环境质量具有重要作用。然而,我国自然保护区生态环境质量变化及其对自然因素与人类活动的响应规律还不清晰,理解这些规律对我国的生态文明建设以及生物多样性的保护具有重要意义。基于2001—2019年中国历史高分辨率生态环境质量数据CHEQ数据集以及自然因素,利用Theil-Sen Median趋势分析、Mann-Kendall检验以及多元回归残差分析等方法,探究了2001—2019年中国自然保护区的生态环境质量时空变化特征及其对自然因素与人类活动驱动因素的响应。结果表明：(1)我国自然保护区的CHEQ指数呈现多阶段波动变化,总体呈小幅度下降趋势,平均趋势率为-0.54×10^-3/a;在空间上,中国自然保护区CHEQ变化趋势值呈“南高北低,东高西低”的分布格局;(2)自然因素与人类活动的共同作用是我国自然保护区生态环境质量恶化的主要原因,且恶化区域主要分布在自然保护区的实验区和缓冲区。其中自然因素对我国自然保护区生态环境质量变化的影响在-3×10^-3/a—0/a之间,人类活动的影响在-1×10^-3     

关帝山云杉次生林树木径向生长的空间关联及其影响因子

以关帝山4 hm²云杉次生林样地为研究对象,按照CTFS(Center for Tropical Forest Science)技术规范对样地树木进行连续定位监测。利用2010至2015年间样地主要树种生长量观测数据,结合地形、土壤等环境因子调查及采样测定数据,分析了树木种群径向生长的空间关联性及其随生境的变化,并探讨了树木种群径向生长的影响因素。结果表明,青杄、华北落叶松、红桦、白桦和辽东栎为云杉次生林主要树种,在样地4个生境型(山脊生境、低海拔缓坡生境、高海拔缓坡生境、低洼地陡坡生境)中均有分布且呈现不同的径级结构。标记相关函数分析显示,同一生境型中,5树种径向生长的空间关联性各异;对于同一树种,径向生长的空间自相关性不仅具有尺度依赖性,同时生境型的不同导致树木径向生长的空间关联性发生变化。线性混合效应模型分析显示,初始胸径对树木径向生长的显著正效应在样地各类生境型的所有种群中普遍存在;生物因子对树木径向生长的显著影响只在特定生境型的青杄种群中被检测到,表明树木径向生长受同种邻体影响,但其影响显著性因树种而异;环境因子中,海拔和凹凸度对树木径向生长呈显著负效应...     

2000—2019年四川省植被恢复成效与影响因素

国家实施天然林资源保护工程与退耕还林等生态建设工程,为构筑长江上游生态屏障、促进长江流域经济可持续发展做出了突出贡献;评估退耕还林等生态工程实施后植被恢复成效及影响因素是促进区域植被恢复优化与生态环境改善的关键一步。基于MODIS MOD13Q1数据,应用Theil Sen斜率与Mann-Kendall趋势检验、“基线”评价方法、时空地理加权回归模型等量化不同时间尺度的植被时空变化、恢复成效和恢复机制。结果表明(1)植被覆盖状况良好,截止2019年底,四川省91%的区域植被出现增长,四川盆地东北部、四川省南部地区以及东南部乌蒙山、川西北高原地区植被覆盖较高;成都市内以及周围市区植被覆盖率较低。(2)植被恢复成效时空差异显著,占全省面积98.68%的区域植被恢复成效明显,高值区面积占比71.47%,集中于除成都平原外的四川省绝大部分区域。(3)气候变化对植被变化的影响以不显著为主,气温、降水对四川省植被恢复影响微弱,海拔和>35°坡度面积比等地理环境因子则以弱抑制作用为主。(4)在相对平稳的气候背景下,人均财政支出、耕地面积与人均GDP所代表的社会经济因素是植被恢复成效改善的重要影...     

Identification of tyrosines 154 and 307 in the extracellular domain and 653 and 766 in the intracellular domain as phosphorylation sites in the heparin-binding fibroblast growth factor receptor tyrosine kinase (flg).

Four tyrosine residues have been identified as phosphorylation sites in the tyrosine kinase isoform of the heparin-binding fibroblast growth factor receptor flg (FGF-R1). Baculoviral-insect cell-derived recombinant FGF-R1 was phosphorylated and fragmented with trypsin while immobilized on heparin-agarose beads. Phosphotyrosine peptides were purified by chromatography on immobilized anti-phosphotyrosine antibody and analyzed by Edman degradation and electrospray tandem mass spectrometry. Tyrosine residue 653, which is in a homologous spatial position to major autophosphorylation sites in the catalytic domain of the src and insulin receptor kinases, is the major intracellular FGF-R1 phosphorylation site. Residue 766 in the COOH-terminus outside the kinase domain is a secondary site. Tyrosine residues 154 and 307, which are in the extracellular domain of transmembrane receptor isoforms and are in an unusual sequence context for tyrosine phosphorylation, were also phosphorylated.