The aim of this study was to explore the effects and mechanisms of different starvation treatments on the compensatory growth of Acipenser dabryanus. A total of 120 fish (60·532 (sem 0·284) g) were randomly assigned to four groups (fasting 0, 3, 7 or 14 d and then refed for 14 d). During fasting, middle body weight decreased significantly with prolonged starvation. The whole-body and muscle composition, serum biochemical indexes, visceral indexes and digestive enzyme activities had been effected with varying degrees of changes. The growth hormone (GH) level in serum was significantly increased in 14D; however, insulin-like growth factor-1 (IGF-1) showed the opposite trend. The neuropeptide Y (npy) mRNA level in brain was significantly improved in 7D; peptide YY (pyy) mRNA level in intestine was significantly decreased during fasting. After refeeding, the final body weight, percentage weight gain, specific growth rate, feed intake, feed efficiency and protein efficiency ratio showed no difference between 0D and 3D. The changes of whole-body and muscle composition, serum biochemical indexes, visceral indexes and digestive enzyme activities had taken place in varying degrees. GH levels in 3D and 7D were significantly higher than those in the 0D; the IGF-1 content decreased significantly during refeeding. There was no significant difference in npy and pyy mRNA levels. These results indicated that short-term fasting followed by refeeding resulted in full compensation and the physiological and biochemical effects on A. dabryanus were the lowest after 3 d of starvation and 14 d of refeeding. Additionally, compensation in A. dabryanus may be mediated by appetite genes and GH, and the degree of compensation is also affected by the duration of starvation.

Low-protein diet plus ketoacids (LPD+KA) has been reported to decrease proteinuria in patients with chronic kidney diseases (CKD). However, the mechanisms have not been clarified. As over-activation of intrarenal renin–angiotensin system (RAS) has been shown to play a key role in the progression of CKD, the current study was performed to investigate the direct effects of LPD+KA on intrarenal RAS, independently of renal haemodynamics. In this study, 3/4 subtotal renal ablated rats were fed 18 % normal-protein diet (Nx-NPD), 6 % low-protein diet (Nx-LPD) or 5 % low-protein diet plus 1 % ketoacids (Nx-LPD+KA) for 12 weeks. Sham-operated rats fed NPD served as controls. The level of proteinuria and expression of renin, angiotensin II (AngII) and its type 1 receptors (AT1R) in the renal cortex were markedly higher in Nx-NPD group than in the sham group. LPD+KA significantly decreased the proteinuria and inhibited intrarenal RAS activation. To exclude renal haemodynamic impact on intrarenal RAS, the serum samples derived from the different groups were added to the culture medium of mesangial cells. It showed that the serum from Nx-NPD directly induced higher expression of AngII, AT1R, fibronectin and transforming growth factor-β1 in the mesangial cells than in the control group. Nx-LPD+KA serum significantly inhibited these abnormalities. Then, proteomics and biochemical detection suggested that the mechanisms underlying these beneficial effects of LPD+KA might be amelioration of the nutritional metabolic disorders and oxidative stress. In conclusion, LPD+KA could directly inhibit the intrarenal RAS activation, independently of renal haemodynamics, thus attenuating the proteinuria in CKD rats.

It has been postulated that aging is the consequence of an accelerated accumulation of somatic DNA mutations and that subsequent errors in the primary structure of proteins ultimately reach levels sufficient to affect organismal functions. The technical limitations of detecting somatic changes and the lack of insight about the minimum level of erroneous proteins to cause an error catastrophe hampered any firm conclusions on these theories. In this study, we sequenced the whole genome of DNA in whole blood of two pairs of monozygotic (MZ) twins, 40 and 100 years old, by two independent next-generation sequencing (NGS) platforms (Illumina and Complete Genomics). Potentially discordant single-base substitutions supported by both platforms were validated extensively by Sanger, Roche 454, and Ion Torrent sequencing. We demonstrate that the genomes of the two twin pairs are germ-line identical between co-twins, and that the genomes of the 100-year-old MZ twins are discerned by eight confirmed somatic single-base substitutions, five of which are within introns. Putative somatic variation between the 40-year-old twins was not confirmed in the validation phase. We conclude from this systematic effort that by using two independent NGS platforms, somatic single nucleotide substitutions can be detected, and that a century of life did not result in a large number of detectable somatic mutations in blood. The low number of somatic variants observed by using two NGS platforms might provide a framework for detecting disease-related somatic variants in phenotypically discordant MZ twins.

Energetic electron beam generation from a thin foil target by the ponderomotive force of an ultra-intense circularly polarized laser pulse is investigated. Two-dimensional particle-in-cell (PIC) simulations show that laser pulses with intensity of 1022–1023 Wcm−2 generate about 1–10 GeV electron beams, in agreement with the prediction of one-dimensional theory. When the laser intensity is at 1024–1025 Wcm−2, the beam energy obtained from PIC simulations is lower than the values predicted by the theory. The radiation damping effect is considered, which is found to become important for the laser intensity higher than 1025 Wcm−2. The effect of laser focus positions is also discussed.

It is well known that c-Jun N-terminal kinase (JNK) plays pivotal roles in various mitotic events, but its function in mammalian oocyte meiosis remains unknown. In this study, we found that no specific JNK2 signal was detected in germinal vesicle stage. JNK2 was associated with the spindles especially the spindle poles and cytoplasmic microtubule organizing centers at prometaphase I, metaphase I, and metaphase II stages. JNK2 became diffusely distributed and associated with the midbody at telophase I stage. Injection of myc-tagged JNK2α1 mRNA into oocytes also revealed its localization on spindle poles. The association of JNK2 with spindle poles was further confirmed by colocalization with the centrosomal proteins, γ-tubulin and Plk1. Nocodazole treatment showed that JNK2 may interact with Plk1 to regulate the spindle assembly. Then we investigated the possible function of JNK2 by JNK2 antibody microinjection and JNK specific inhibitor SP600125 treatment. These two manipulations caused abnormal spindle formation and decreased the rate of first polar body (PB1) extrusion. In addition, inhibition of JNK2 resulted in impaired localization of Plk1. Taken together, our results suggest that JNK2 plays an important role in spindle assembly and PB1 extrusion during mouse oocyte meiotic maturation.

Composite Sensitive High Resolution Ion Microprobe (SHRIMP) U–Pb zircon and 40Ar–39Ar step-heating biotite-hornblende ages are used to provide constraints on the timing and origin of the felsic gneissic rocks in the Baiyunshan Mountains region and to elucidate their tectonothermal history. SHRIMP dating and CL imaging of zircons give magmatic zircon crystallization ages between Late Ordovician and Early Silurian (c. 453.5 Ma, 446 Ma, and 439 Ma) for three representative felsic gneisses, suggesting that most of the Baiyunshan gneiss cannot represent basement rocks of the Cathaysia Block as previously thought. Including the present age information, a synthesis of available age data for regional Wuyun (Wuyi-Yunkai) events reflects the emergence of orogen-wide magmatism that could be syn-orogenic and have occurred mainly between 460 and 420 Ma in the South China Block. Inherited zircons are abundant, with ages clustering at late Mesoproterozoic (1189–1017 Ma) and middle Mesoproterozoic (772 Ma), which reveals that the Baiyunshan orthogneiss samples a crustal basement containing significant igneous or recycled components related to the Rodinia amalgamation and break-up. A SHRIMP date of 212 ± 12 Ma from a white rim of zircon provides evidence for metamorphic overprinting of an Indosinian tectonothermal event on the Baiyunshan gneiss. Incremental heating experiments with six biotite samples and one hornblende sample from a variety of metamorphic rocks yielded two distinct 40Ar–39Ar age groups: 150–155 and 94–98 Ma. The older ages are similar to zircon U–Pb dates for widespread granitic intrusions in central Guangdong. We attribute them to Late Jurassic magmatism-induced thermal resetting of the biotite K–Ar system. On the other hand, the younger age group is interpreted to record either cooling through the biotite closure temperature of ~300–350 °C or a second resetting of biotite Ar isotopes at c. 94–98 Ma due to contemporaneous magmatic activity. Our present age data suggest that the Maofengshan orthogneiss was exhumed to 8 to 10 km crustal levels at c. 150 Ma, whereas the eastward components of gneissic rock masses appear to have passed upward through the same crustal depth synchronously or later (by c. 94 Ma). Exhumation of middle crustal-level rocks in the study area since c. 155 Ma is roughly coeval with exhumation of gneissic rocks from elsewhere in the Wuyun Orogen, suggesting a large-scale mechanism for the exhumation pulse related to the Yanshanian extensional tectonic regime.

Primers bearing restriction enzyme sites for EcoR I and Hind III were designed according to the known partial cDNA sequence for gibberellin-induced cysteine-rich protein and were then used to amplify the full-length open reading frame (ORF) and signal peptide-truncated fragment of the gcgasa gene. Two fragments with lengths 319 and 238 bp were obtained and were further cloned into plasmid pET-32(a). Following transformation into Escherichia coli BL21(DE3), the fusion proteins were observed to appear at ~26.0 and 25.2 kDa after induction from 1 mmol/l isopropyl-beta-D-thiogalactopyronoside (IPTG). The results of sodium dodecyl sulphate polyacrylamide gel electrophoresis (SDS-PAGE) and transmission electron microscopy (TEM) of an ultra-thin section revealed that the presence of signal peptide gave rise to the formation of an inclusion body located in the periplasmic space; however, the absence of signal peptide greatly enhanced the solubility of the target protein. The expressed soluble protein was further purified by Ni2+-NTA affinity chromatography and gel filtration methods.