M?ssbauer study of the native, reduced and substrate-reacted Desulfovibrio gigas aldehyde oxido-reductase.

The Desulfovibrio gigas aldehyde-oxido-reductase contains molybdenum and iron-sulfur clusters. M?ssbauer spectroscopy was used to characterize the iron-sulfur clusters. Spectra of the enzyme in its oxidized, partially reduced and benzaldehyde-reacted states were recorded at different temperatures and applied magnetic fields. All the iron atoms in D. gigas aldehyde oxido-reductase are organized as [2Fe-2S] clusters. In the oxidized enzyme, the clusters are diamagnetic and exhibit a single quadrupole doublet with parameters (delta EQ = 0.62 +/- 0.02 mm/s and delta = 0.27 +/- 0.01 mm/s) typical for the [2Fe-2S]2+ state. M?ssbauer spectra of the reduced clusters also show the characteristics of a [2Fe-2S]1+ cluster and can be explained by a spin-coupling model proposed for the [2Fe-2S] cluster where a high-spin ferrous ion (S = 2) is antiferromagnetically coupled to a high-spin ferric ion (S = 5/2) to form a S = 1/2 system. Two ferrous sites with different delta EQ values (3.42 mm/s and 2.93 mm/s at 85 K) are observed for the reduced enzyme, indicating the presence of two types of [2Fe-2S] clusters in the D. gigas enzyme. Taking this observation together with the re-evaluated value of iron content (3.5 +/- 0.1 Fe/molecule), it is concluded that, similar to other Mo-hydroxylases, the D. gigas aldehyde oxido-reductase also contains two spectroscopically distinguishable [2Fe-2S] clusters.     

D type cyclins associate with multiple protein kinases and the DNA replication and repair factor PCNA.

Human cyclin D1 has been associated with a wide variety of proliferative diseases but its biochemical role is unknown. In diploid fibroblasts we find that cyclin D1 is complexed with many other cellular proteins. Among them are protein kinase catalytic subunits CDK2, CDK4 (previously called PSK-J3), and CDK5 (also called PSSALRE). In addition, polypeptides of 21 kd and 36 kd are identified in association with cyclin D1. We show that the 36 kd protein is the proliferating cell nuclear antigen, PCNA. Cyclin D3 also associates with multiple protein kinases, p21 and PCNA. It is proposed that there exists a quaternary complex of D cyclin, CDK, PCNA, and p21 and that many combinatorial variations (cyclin D1, D3, CDK2, 4, and 5) may assemble in vivo. These findings link a human putative G1 cyclin that is associated with oncogenesis with a well-characterized DNA replication and repair factor.     

The differential distribution of vasoactive intestinal polypeptide in the normal human female genital tract

Summary VIP-like immunoreactive material is present in the female reproductive tract, with a distinct pattern of distribution. The highest concentrations of extractable material and immunoreactive nerve fibres were found in the cervix and vagina. In the cervix these fibres were seen below the surface epithelium and around cervical glands as well as in association with blood vessels and smooth muscle bundles. In the vagina the nerve fibres were most abundant in the superficial regions of the lamina propria. Scattered fibres were also present in the rest of the uterus and in the fallopian tubes. Chromatographic evidence indicates that this VIP-like material is of a similar molecular size to that extracted from other organs. Possible roles for VIP in the regulation of myometrial activity and of cervical and vaginal dilation and secretion are proposed.     

Fluorescence-microscopical demonstration of a population of gastro-intestinal nerve fibres with a selective affinity for Quinacrine

Summary A population of nerve fibres in the gastro-intestinal tract of mice showing a high affinity for quinacrine was revealed by fluorescence microscopy. Similar results were obtained in rats and guinea pigs. Whole-mounts of sheets of the smooth muscle layer following incubation in 10^-6-10^-7 M quinacrine for 15–60 min revealed fine fluorescent varicose nerve fibers in the myenteric plexus of Auerbach both around nerve cell bodies and in the interconnecting strands. Many fibers were also present between the strands of the plexus, especially running parallel to the circular muscle layer. Such fibers were not seen in similarly quinacrine-incubated irides. A proportion of the cell bodies in Auerbach's plexus also showed quinacrine accumulation. These cells were apparently smaller neurons, sometimes with fluorescent processes. Intraperitoneal injections of quinacrine failed to demonstrate nerve fibers, but some cell bodies in Auerbach's plexus were positive. Subsequent paraformaldehyde treatment for monoamine visualization showed persistent adrenergic nerve terminals in the intestine and iris. These nerves seemed to be fewer and had a more yellow fluorescence than normally. The identity of the quinacrine-positive fibers is discussed with respect to recent suggestions that purinergic, substance P, enkephalin, and somatosin-containing nerves, in addition to adrenergic and cholinergic nerves, are present in the gut wall.Supported by the Swedish Medical Research Council (04X-03185). Magnus Bergvalls Stiftelse and Karolinska Institutets Fonder. For generous gifts of Mepacrine we thank Winthrop, Skärholmen, Stockholm, Sweden. The skilful technical assistance of Miss Gerd Boetius and Miss Maud Eriksson is gratefully acknowledged     

基于MaxEnt模型的甘肃安西极旱荒漠国家级自然保护区北山羊生境评估

明晰甘肃安西极旱荒漠国家级自然保护区珍稀濒危物种北山羊的分布格局,并阐释气候变化和人类活动对北山羊的影响,对今后北山羊生境管理和物种保护具有重要意义。基于北山羊实测分布点记录和环境变量数据,结合MaxEnt模型和ArcGIS空间分析功能,利用CMIP6的8个气候模式均值预测中度发展路径（SSP2-4.5）下,基准期（1970-2000年）和未来气候（2041-2060年、2081-2100年）变化情景下,甘肃安西极旱荒漠国家级自然保护区北山羊的潜在适生区分布范围及变化,并综合贡献率和置换重要性值对北山羊生境选择关键环境因子进行了分析。研究结果表明：（1） MaxEnt模型的预测精度较高,三种气候条件下ROC曲线下面积（AUC,Area Under Curve）>0.97,且真实技巧统计（TSS,True Skill Statistic）>0.90,模拟结果可靠。（2）影响北山羊生境选择的主要环境因子为气候条件（降水量季节性变异系数和等温性）、海拔和人为干扰（距泉和居名点距离）。水是保护区北山羊生存的最基本要素,气候条件共同控制北山羊生境条件。此外,北山羊习性决定其生境宜选择高海拔和远离人类活动影响地区。（3）基准期保护区北山羊主要分布在北片和南片高海拔山区,面积365.77 km²（占整个保护区的4.31%）,北山羊适生区面积北片>南片、中高等适生区主要位于保护区北片。（4） CMIP6未来气候变化情景下,随着保护区生态环境改善和濒危物种保护措施的实施,北山羊潜在适生区面积呈增加趋势,但是受北山羊近亲繁殖的影响,整体上北山羊数量和适生区面积增加并不显著且有向南部及高海拔地区转移趋势。     

淮河流域暖季极端高温干旱复合事件的演变特征及其与气候和植被的关系

使用淮河流域1981年至2020年的149个气象站点的气温和相对湿度数据,分析了流域暖季极端高温干旱复合事件(Compound Drought and Heat Events,CDHEs)的时空演变特征,并通过趋势分析和相关分析法探讨了CDHEs与气候和植被的关系。结果表明:①CDHEs的发生日数在年代际尺度上呈现明显的增加趋势,并且范围扩大,频发区逐渐向淮河流域中西部移动;②在年际尺度上,CDHEs随时间序列呈显著的波动上升趋势,空间分布上以西北部为中心向四周递减。连续CDHEs事件呈年际变化,最大2至4天的连续事件存在波动,2019年达到高峰,并且在流域内零散或成片出现;③在月际尺度上,CDHEs的发生日数在6月最多,其次是5月、7月、9月和8月。淮河流域入汛前的旱情和入汛后的旱涝急转都容易导致CDHEs发生,而且随着月际变化向南移动;④CDHEs对水热条件和大气环流具有特别的敏感性。在850hPa反气旋和500hPa显著高压异常的控制下,高温、低湿、高蒸发和降水少的气候背景有利于淮河地区CDHEs的形成,尤其是在淮河中西部地区。因此,CDHEs的发生与气候变化密切相关;⑤CDHEs与植被生长也存在显著关系。CDHEs与GPP呈显著的负相关,而与NDVI呈显著的正相关,显著地区的土地类型以耕地和城乡、工矿、居民用地为主。GPP和NDVI的不同步可能是因为多种因素的非线性相互作用,而不仅仅是单一因素的影响。此外,对于GPP和NDVI来说,土壤含水量至关重要。总之,本文对淮河流域CDHEs的时空分布特征进行了深入研究,并探讨了其与气候和植被的关系。研究结果可以为该地区的气象灾害防御和生态环境保护提供科学依据和参考。     

DAZL regulates proliferation of human primordial germ cells by direct binding to precursor miRNAs and enhances DICER processing activity

Understanding the molecular and cellular mechanisms of human primordial germ cells (hPGCs) is essential in studying infertility and germ cell tumorigenesis. Many RNA-binding proteins (RBPs) and non-coding RNAs are specifically expressed and functional during hPGC developments. However, the roles and regulatory mechanisms of these RBPs and non-coding RNAs, such as microRNAs (miRNAs), in hPGCs remain elusive. In this study, we reported a new regulatory function of DAZL, a germ cell-specific RBP, in miRNA biogenesis and cell proliferation. First, DAZL co-localized with miRNA let-7a in human PGCs and up-regulated the levels of >100 mature miRNAs, including eight out of nine let-7 family, miR21, miR22, miR125, miR10 and miR199. Purified DAZL directly bound to the loops of precursor miRNAs with sequence specificity of GUU. The binding of DAZL to the precursor miRNA increased the maturation of miRNA by enhancing the cleavage activity of DICER. Furthermore, cell proliferation assay and cell cycle analysis confirmed that DAZL inhibited the proliferation of in vitro PGCs by promoting the maturation of these miRNAs. Evidently, the mature miRNAs up-regulated by DAZL silenced cell proliferation regulators including TRIM71. Moreover, DAZL inhibited germline tumor cell proliferation and teratoma formation. These results demonstrate that DAZL regulates hPGC proliferation by enhancing miRNA processing.