Monitoring of Ubiquitin-proteasome Activity in Living Cells Using a Degron (dgn)-destabilized Green Fluorescent Protein (GFP)-based Reporter Protein

Proteasome is the main intracellular organelle involved in the proteolytic degradation of abnormal, misfolded, damaged or oxidized proteins ^{1, 2}. Maintenance of proteasome activity was implicated in many key cellular processes, like cell''s stress response ³, cell cycle regulation and cellular differentiation ⁴ or in immune system response ⁵. The dysfunction of the ubiquitin-proteasome system has been related to the development of tumors and neurodegenerative diseases ^{4, 6}. Additionally, a decrease in proteasome activity was found as a feature of cellular senescence and organismal aging ^{7, 8, 9, 10}. Here, we present a method to measure ubiquitin-proteasome activity in living cells using a GFP-dgn fusion protein. To be able to monitor ubiquitin-proteasome activity in living primary cells, complementary DNA constructs coding for a green fluorescent protein (GFP)–dgn fusion protein (GFP–dgn, unstable) and a variant carrying a frameshift mutation (GFP–dgnFS, stable ¹¹) are inserted in lentiviral expression vectors. We prefer this technique over traditional transfection techniques because it guarantees a very high transfection efficiency independent of the cell type or the age of the donor. The difference between fluorescence displayed by the GFP–dgnFS (stable) protein and the destabilized protein (GFP-dgn) in the absence or presence of proteasome inhibitor can be used to estimate ubiquitin-proteasome activity in each particular cell strain. These differences can be monitored by epifluorescence microscopy or can be measured by flow cytometry.     

Polymorphism and heterogeneity of transferrins in some species of the fish family Cyprinidae

In fish of the family Cyprinidae extensive polymorphism and heterogeneity of serum transferrins were found. Ten variants of transferrins were detected in barbel, 9 in dace and bleak, 7 in chub and bream, 6 in rudd, 5 in roach, white bream, silver carp, big head and crucian carp, 3 in tench, and 2 variants in nase, ide and goldfish. All the variants observed bound radioactive iron. The phenotype patterns indicated a simple genetic determination, by a set of codominant alleles at one locus, and this even in tetraploid species. Transferrins of some species were partly isolated. The transferrins of all 22 species analysed were heterogeneous and homozygous pheno-types had 1 to 6 zones of various intensities, binding ⁵⁹Fe. In barbel both single-zone and two-zone variants were present and transferrins of roach had variable heterogeneity. Sialic acid was found only in transferrins of silver carp, big head and in the two-zone variants of barbel. The occurrence of phenotypes with single and double zones of transferrins in barbel indicates the possibility of genetic determination of the inability of single-zone variants to bind sialic acid.     

二倍体马铃薯耐盐品种鉴定的生理指标测定

以不同耐盐性的二倍体马铃薯富利亚（Solanum phureja, PHU） 和窄刀薯假stenotomum,STN）杂种（PHU．STN）无性系为材料,在离体条件下用0（对照）、10、20、30mmol·L^-1NaCl进行胁迫处理,测定试管苗叶的电导率、丙二醛和脯氨酸含量,结果表明,随着盐浓度的升高,这3个生理指标的相对值均逐渐升高,耐盐性不同的二倍体马铃薯差异极显著。表明电导率、丙二醛和脯氨酸含量可以作为二倍体马铃薯耐盐性鉴定的生理指标。     

Mitochondrial cytochrome b Sequence Variation and Phylogenetics of the Highly Specialized Schizothoracine Fishes (Teleostei: Cyprinidae) in the Qinghai-Tibet Plateau

The complete 1140 bp mitochondrial cytochrome b sequences were obtained from 39 individuals representing five species of all four genera of highly specialized schizothoracine fishes distributed in the Qinghai-Tibet plateau. Sequence variation of the cytochrome b gene was surveyed among the 39 individuals as well as three primitive schizothoracines and one outgroup. Phylogenetic analysis suggested that the group assignment based on 1140 bp of the cytochrome b sequence is obviously different from previous assignments, and the highly specialized schizothoracine fishes (Schizopygopsis pylzovi, Gymnocypris przewalskii, G. eckloni, Chuanchia labiosa, and Platypharodon extremus) form a monophyletic group that is sister to the clade formed by the primitive schizothoracine fishes (Schizothorax prenanti, S. pseudaksaiensis, and S. argentatus). The haplotypes of Schizopygopsis pylzovi and G. przewalskii were paraphyletic based on cytochrome b data, which most likely reflected incomplete sorting of mitochondrial DNA lineages. The diploid chromosome numbers of Schizothoracinae were considered in phylogenetic analysis and provided a clear pattern of relationships. Molecular dating estimated for highly specialized schizothoracine fishes suggested that the highly specialized schizothoracine fishes diverged in the late Miocene Pliocene to Pleistocene (4.5 × 10⁴–4.05 × 10⁶ years BP). The relationship between the cladogenesis of highly specialized schizothoracine fishes and geographical events of the Qinghai-Tibet plateau is discussed.