北京地区蒿柳的开花物候期及单花序开放过程中花粉活力和柱头可授性变化

Flowering phenology and flowering dynamics of female and male inflorescences of Salix viminalis Linn. in Beijing were observed in 2015 and 2016, and changes in pollen activity and stigma receptivity were also investigated. The results show that early flowering stage of S. viminalis in Beijing is happened in early?March, flowering period is 11-18 d, and flowering pattern is the first opening type of male flower. Flowering period of single inflorescence in male and female plants is 10-15 d and 8-10 d, respectively, which can be divided into five stages:emerging color stage, initial flowering stage, half flowering stage, full flowering stage and withered stage. Flowering date of male plant is earlier about 3-4 d than that of female plant. However, the difference of full flowering stage between male and female plants is only 1 d. Pollen germination rate and stigma receptivity show a trend of firstly increasing then decreasing during blossom process. Pollen germination rate reaches the highest of 72% at full flowering stage, and stigma receptivity is more than 90% at half and full flowering stages. Therefore, it is suggested that pollen collection and pollination in mid?March can improve success rate of cross breeding of S. viminalis.     

Dynamics of soil organic carbon storage following restoration of grassland on Yunwu Mountain

Grassland recovery and reconstruction are critical to ecological restoration in the Chinese Loess Plateau (CLP). Investigating changes in soil organic carbon density (SOCD), soil organic carbon (SOC) storage, and the rate of SOC sequestration is very important to assess the effect of ecological recovery and estimate the capacity of soil carbon sequestration. Here, we present the data of SOCD, SOC storage, and SOC sequestration rate from grasslands conversion from farmlands in the CLP. Our results indicate that: (1) The average SOCD (0–100 cm) in sites continued cultivation (CC), cultivation abandonment at 1999 (AC-99) and cultivation abandonment at 1989 (AC-89) is 6.00, 21.64 and 22.23 kg m^?2, respectively. SOCD in sites AC-99 and AC-89 is significantly higher than that in site CC and the average SOCD of China (10.53 kg m^?2), which indicates that vegetation restoration is benefit to increase soil carbon storage as well as preserve soil and water in this area. (2) The SOC storage (0–100 cm) in sites CC, AC-99 and AC-89 is 60.02, 216.35 and 222.32 kg m^?2, respectively. Results of ANOVA indicate that SOC storage of AC-99 is significantly higher than that of CC, while SOC storage of AC-89 is significantly higher than that of AC-99 at the depth of 0–50 cm (P < 0.001). It suggests that the capability of soil carbon sequestration increases after vegetation restoration, which is mainly due to the increase of plant roots. (3) The rate of SOC sequestration varies at different depths, which is high at the depth of 0–50 cm while low at the depth of 50–100 cm. This is probably due to the accumulation of plant root in the surface layer, which is the main controlling factor of SOC in this area. Our results indicate that the SOCD and SOC storage increase with vegetation restoration in our study site significantly.     

Dynamics of soil organic carbon storage following restoration of grassland on Yunwu Mountain

Grassland recovery and reconstruction are critical to ecological restoration in the Chinese Loess Plateau (CLP). Investigating changes in soil organic carbon density (SOCD), soil organic carbon (SOC) storage, and the rate of SOC sequestration is very important to assess the effect of ecological recovery and estimate the capacity of soil carbon sequestration. Here, we present the data of SOCD, SOC storage, and SOC sequestration rate from grasslands conversion from farmlands in the CLP. Our results indicate that: (1) The average SOCD (0–100 cm) in sites continued cultivation (CC), cultivation abandonment at 1999 (AC-99) and cultivation abandonment at 1989 (AC-89) is 6.00, 21.64 and 22.23 kg m^?2, respectively. SOCD in sites AC-99 and AC-89 is significantly higher than that in site CC and the average SOCD of China (10.53 kg m^?2), which indicates that vegetation restoration is benefit to increase soil carbon storage as well as preserve soil and water in this area. (2) The SOC storage (0–100 cm) in sites CC, AC-99 and AC-89 is 60.02, 216.35 and 222.32 kg m^?2, respectively. Results of ANOVA indicate that SOC storage of AC-99 is significantly higher than that of CC, while SOC storage of AC-89 is significantly higher than that of AC-99 at the depth of 0–50 cm (P < 0.001). It suggests that the capability of soil carbon sequestration increases after vegetation restoration, which is mainly due to the increase of plant roots. (3) The rate of SOC sequestration varies at different depths, which is high at the depth of 0–50 cm while low at the depth of 50–100 cm. This is probably due to the accumulation of plant root in the surface layer, which is the main controlling factor of SOC in this area. Our results indicate that the SOCD and SOC storage increase with vegetation restoration in our study site significantly.     

A Nficrocalorimetry and Spectroscopy Study on the Interaction of BSA with 2,2′-Bipyridine Octylglycinato Palladium（Ⅱ） Nitrate

The interaction of bovine serum albumin (BSA) with a new palladium(Ⅱ) complex [ Pd(bpy) (Oct-Gly)] NO3 (bpy, 2,2′-bipyridine; Oct-Gly, octyl-glycine) was studied by isothermal titration UV-visible spectrophotometry and microcalorimetry in 30 mmol/L Tris buffer, pH 7.0. There is a set of 18 binding sites for this complex on BSA at 300 and 310 K with positive cooperativity in the binding process. The Hill coefficients at 300 and 310 K are 2.2 and 2.4, respectively. The binding of this palladium complex on BSA is endothermic with mean association binding constant of 21.0 and 16.4(mmol/L)^-1 at 300 and 310 K, respectively. The complex can denature the protein as surfactants. The stability of BSA in the interaction study with the complex is 84 and 58 kJ/mol at 300 and 310 K, respectively. Also, the enthalpy of BSA denaturation due to the interaction with the complex is 842 kJ/mol.     

A Stable Upstream Stem-loop Structure Enhances Selection of the First 5′-ORF-AUG as a Main Start Codon for Translation Initiation of Human ACAT1 mRNA

Human ACAT1 cDNA K1 was first cloned and functionally expressed in 1993. There are two adjacent in-frame AUG codons, AUG1397-1399 and AUG1415-1417, at 5′-terminus of the open reading frame (ORF,nt 1397-3049) of human ACAT1 mRNA corresponding to cDNA K1. In current work, these two adjacent in-frame AUGs at 5′-terminus of the predicted ORF (5′-ORF-AUGs) as start codons for translation initiation of human ACAT1 mRNA were characterized in detail. Codon mutations indicated that both of these two adjacent 5′-ORF-AUGs can be selected as start codons but the first 5′-ORF-AUG1397-1399 is a main start codon consistent with that of the predicted ORF of human ACAT1 mRNA. Further deletion and mutation analyses demonstrated that a stable upstream stem-loop structure enhanced the selection of the first 5′-ORF-AUG1397-1399 as a main start codon, in addition to upstream nucleotide A in the -3 position, which is a key site of Kozak sequence. In addition, result of ACAT1 enzymatic activity assay showed no obvious difference between these two ACAT1 proteins respectively initiated from the two adjacent 5′-ORF-AUGs. This work showed that astable upstream stem-loop structure could modulate the start codon selection during translation initiation of mRNAs that contain adjacent multi-5′-ORF-AUGs.     

C-Terminus-Mediated Voltage Gating of Arabidopsis Guard Cell Anion Channel QUAC1

Anion transporters in plants play a fundamental role in volume regulation and signaling. Currently, two plasma membrane-located anion channel familiesmSLAC/SLAH and ALMTmare known. Among the ALMT family, the root-expressed ALuminium-activated Malate Transporter 1 was identified by comparison of aluminum-tolerant and Al3＋-sensitive wheat cultivars and was subsequently shown to mediate voltage-independent malate currents. In con- trast, ALMT12/QUAC1 （QUickly activating Anion Channel1） is expressed in guard cells transporting malate in an Al3＋- insensitive and highly voltage-dependent manner. So far, no information is available about the structure and mechanism of voltage-dependent gating with the QUAC1 channel protein. Here, we analyzed gating of QUACl-type currents in the plasma membrane of guard cells and QUACl-expressing oocytes revealing similar voltage dependencies and activation- deactivation kinetics. In the heterologous expression system, QUAC1 was electrophysiologically characterized at increas- ing extra- and intracellular malate concentrations. Thereby, malate additively stimulated the voltage-dependent QUAC1 activity. In search of structural determinants of the gating process, we could not identify transmembrane domains com- mon for voltage-sensitive channels. However, site-directed mutations and deletions at the C-terminus of QUAC1 resulted in altered voltage-dependent channel activity. Interestingly, the replacement of a single glutamate residue, which is con- served in ALMT channels from different clades, by an alanine disrupted QUAC1 activity. Together with C- and N-terminal tagging, these results indicate that the cytosolic C-terminus is involved in the voltage-dependent gating mechanism of QUAC1.     

羟基脲诱导前后HEL细胞内GATA转录因子与人β—类珠蛋白基因调控元件 …

HEL cells, a human erythroleukemia cell line, expressing mainly the gamma-globin genes, small amount of epsilon-globin gene, but not beta-globin gene. Our previous studies demonstrated that beta-globin gene could be expressed in HEL cells induced by hydroxyurea. However, the molecular mechenism is still unknown. Here the binding patterns of GATA factors (GATA-1 and GATA-2) to the regulatory elements of human beta-globin gene were examined with the nuclear extracts from hydroxyurea-induced and uninduced HEL cells. Our results showed in EMSA assay that GATA factors could bind to the core sequence of HS2(-10681 to -10971 bp), the 3' flanking sequence of HS2 core(-10323 to -10680 bp) and the promoter of human beta-globin gene(+20 to -112 bp). However, the binding patterns between hydroxyurea-induced and uninduced HEL cells were different. Furthermore, by using Western-blot analysis, our data showed that the amount of GATA-2 was decreased in hydroxyurea-induced HEL cells. In contrast to GATA-2, the amount of GATA-1 was increased in hydroxyurea-induced HEL cells. These results showed that the different members of GATA family might play different roles during the differentiation of erythrocytes. GATA-1 may stimulate the differentiation of HEL cells, while GATA-2 can probably inhibit the differentiation of HEL cells.     

羟基脲对人红白血病细胞株中球蛋白基因表达和细胞分化的影响

人红白血病细胞株（ＨＥＬ细胞）中珠蛋白基因表达具有自己的特点。即只表达胚胎型的γ－珠蛋白基因而不表达成人型的β－珠蛋白基因。羟基脲是一种抑制ＤＮＡ的小分子有机化合物。它在临床上被用来治疗地中海盆血和镰刀型贫血。我们的实验结果表明：胡羟基脲浓度增加ＨＥＬ细胞增殖速度减慢。用常规ＲＴ－ＰＣＲ方法和定量ＰＣＲ分析证明,用羟基脲诱导ＨＥＬ细胞后,β－珠蛋白基因表达增加,α－珠蛋白基因表达减少,而γ－珠蛋白     

CACCC and GATA-1 sequences make the constitutively expressed alpha-globin gene erythroid-responsive in mouse erythroleukemia cells.

Although the human alpha-globin and beta-globin genes are co-regulated in adult life, they achieve the same end by very different mechanisms. For example, a transfected beta-globin gene is expressed in an inducible manner in mouse erythroleukemia (MEL) cells while a transfected alpha-globin gene is constitutively expressed at a high level in induced and uninduced MEL cells. Interestingly, when the alpha-globin gene is transferred into MEL cells as part of human chromosome 16, it is appropriately expressed in an inducible manner. We explored the basis for the lack of erythroid-responsiveness of the proximal regulatory elements of the human alpha-globin gene. Since the alpha-globin gene is the only functional human globin gene that lacks CACCC and GATA-1 motifs, we asked whether their addition to the alpha-globin promoter would make the gene erythroid-responsive in MEL cells. The addition of each of these binding sites to the alpha-globin promoter separately did not result in inducibility in MEL cells. However, when both sites were added together, the alpha-globin gene became inducible in MEL cells. This suggests that erythroid non-responsiveness of the alpha-globin gene results from the lack of erythroid binding sites and is not necessarily a function of the constitutively active, GC rich promoter.