SO2的衍生物对泥鳅的急性毒性和染色体损伤研究

SO2是形成酸雨的主要成分之一,SO2对生物的危害主要是通过其进人生物体内产生的代谢产物——亚硫酸钠与亚硫酸氢钠对组织、细胞和生物大分子的作用而实现的。前人的研究结果发现：亚硫酸氢钠能够诱发人外周血淋巴细胞和小鼠骨髓嗜多染红细胞微核的产生。鱼类对化学物质的反应与哺乳动物有很多相似之处,而鱼类中泥鳅具有较高敏感性,它们较之蝌蚪及其他鱼类,具有取材容易.     

锦鸡儿属3种植物的核型研究

以锦鸡儿属中间锦鸡儿、柠条锦鸡儿、狭叶锦鸡儿为材料,用光学显微镜观察了3种锦鸡儿的染色体,按全国第一次植物染色体学术讨论会建议的标准进行了核型分析。结果表明,3种锦鸡儿的体细胞染色体数目2n=16,核型公式分别为:中间锦鸡儿2n=2x=16=10m 6sm、柠条锦鸡儿2n=2x=16=12m 4sm、狭叶锦鸡儿2n=2x=16=14m 2sm,中间锦鸡儿和柠条锦鸡儿的核型属于2A型,狭叶锦鸡儿的核型属于2B型。狭叶锦鸡儿二倍体染色体核型为首次报道。     

Caenorhabditis elegans p97/CDC-48 is crucial for progression of meiosis I

p97/VCP/Cdc48p belongs to the AAA (ATPases associated with diverse cellular activities) family and has been indicated to be required for mitotic M-phase. We previously reported that simultaneous depletion of two p97 homologues, CDC-48.1 and CDC-48.2, in Caenorhabditis elegans caused the complete embryonic lethality, and that a large number of vacuole-like structures were observed in the dead embryos. However, cellular functions of p97 in embryogenesis have not been revealed. In this study, we analyzed effects of p97 depletion on meiotic progression. Simultaneous depletion of both p97 resulted in the formation of aberrant multinucleate cells and sometimes ectopic furrows in embryos. Importantly, meiotic chromosomes were not divided at meiotic metaphase I in p97-depleted embryos, although spindle formation and disassembly occurred. Furthermore, we found that chromosome condensation was significantly reduced in p97-depleted oocytes. Taken these results altogether, we propose that C. elegans p97 plays an important role in the progression of meiosis.     

Molecular systematics and biogeography of Resedaceae based on ITS and trnL-F sequences

The Resedaceae, containing 6 genera and ca. 85 species, are widely distributed in the Old World, with a major center of species diversity in the Mediterranean basin. Phylogenetic analyses of ITS and plastid trnL-trnF sequences of 66 species from all genera of the Resedaceae reveal (1) monophyly of the family, in congruence with preliminary phylogenetic studies; (2) molecular support for the traditional morphological subdivision of the Resedaceae into three tribes according to ovary and placentation types, and carpel number; (3) two monophyletic genera (Caylusea, Sesamoides), and one natural group (core Reseda), which includes the remaining four genera of the family (Ochradenus, Oligomeris, Randonia, Reseda); (4) a monophyletic origin for four of the six taxonomic sections recognized within Reseda (Leucoreseda, Luteola, Glaucoreseda, Phyteuma). Our results lead us to interpret an increment of the basic chromosome number in the family from x=5 to x=6 in at least two independent instances, and a broad representation of polyploids in multiple lineages across phylogenies, including association between octoploids and alien invasion in many parts of the world. Species diversity, endemism number, phylogenetic relationships and sequence divergence in Resedaceae suggest two major centers of differentiation, one in the western Mediterranean, and the other in the eastern Mediterranean and SW Asia. Two independent colonization events to the Canary Islands from Africa are indicated for the two Canarian Reseda endemics.     

Production of mouse fetuses using spermatozoa exposed temporarily to high temperature or continuously to room temperature after freeze-drying in Na+-free/K+-rich EGTA buffer

Present study aimed to determine to what extent freeze-dried spermatozoa were able to withstand high-temperature conditions: transient increase in storage temperature and long-term exposure to room temperature. Mouse spermatozoa were freeze-dried in EGTA/Tris-HCl buffered solution alkalinized using KOH (K-ETBS, pH 7.7), and then stored for up to 7 months at 4 °C or 25 °C. After 2 months’ storage, some of the 4°C-stored spermatozoa were exposed to 40 °C for 1 week or 1 month, then again stored at 4 °C for the remaining storage period. Following storage, rehydrated spermatozoa were injected into mouse oocytes. The resulting zygotes were assessed for chromosome damage, in vitro development up to the blastocyst stage, and post-implantation development to normal fetuses on day 18 of gestation. In storage at 4 °C, one-week exposure to 40 °C had no adverse effect on the chromosome integrity and developmental competence compared to non-exposure to 40 °C (continuous storage at 4 °C). In contrast, one-month exposure to 40 °C caused an increasing level of chromosome damage (36%, P < 0.05) and reduced frequencies of blastocysts (54%, P < 0.05) and normal fetuses (36%, P < 0.05) compared to the frequencies obtained by continuous storage at 4 °C (15%, 82% and 52%, respectively). Storage at 25 °C resulted in accumulation of chromosome damage (27%, P < 0.05), leading to decreased blastocyst formation (63%, P < 0.05). But, the frequency of normal fetus (44%) was not significantly different from that obtained by continuous storage at 4 °C. Consequently, mouse spermatozoa freeze-dried in K-ETBS withstood temporary exposure to 40 °C for 1 week. Chromosome damage accumulated in spermatozoa during storage at 25 °C.     

Disruption of a Conserved CAP-D3 Threonine Alters Condensin Loading on Mitotic Chromosomes Leading to Chromosome Hypercondensation

The condensin complex plays a key role in organizing mitotic chromosomes. In vertebrates, there are two condensin complexes that have independent and cooperative roles in folding mitotic chromosomes. In this study, we dissect the role of a putative Cdk1 site on the condensin II subunit CAP-D3 in chicken DT40 cells. This conserved site has been shown to activate condensin II during prophase in human cells, and facilitate further phosphorylation by polo-like kinase I. We examined the functional significance of this phosphorylation mark by mutating the orthologous site of CAP-D3 (CAP-D3^T1403A) in chicken DT40 cells. We show that this mutation is a gain of function mutant in chicken cells; it disrupts prophase, results in a dramatic shortening of the mitotic chromosome axis, and leads to abnormal INCENP localization. Our results imply phosphorylation of CAP-D3 acts to limit condensin II binding onto mitotic chromosomes. We present the first in vivo example that alters the ratio of condensin I:II on mitotic chromosomes. Our results demonstrate this ratio is a critical determinant in shaping mitotic chromosomes.     

Molecular cytogenetic insights into the evolution of the epiphytic genus Lepismium (Cactaceae) and related genera

Changes in chromosome structure and number play an important role in plant evolution. This was investigated in the Neotropical epiphytic cacti: all Lepismium spp. and some related Rhipsalis spp. Both genera have species with disjunct distributions between the paranas of south‐eastern Brazil and north‐eastern Argentina and the yungas forests of the eastern Andes. Karyotypes, fluorescent banding and fluorescence in situ hybridization (FISH) studies using rDNA probes were performed. A time‐calibrated phylogenetic tree was generated to place the karyological information and biogeographical history in an explicit evolutionary context. All species were 2n = 22 and showed symmetrical karyotypes comprising only metacentric chromosomes of similar sizes. The heterochromatin bands were always associated with chromosome satellites coinciding with the location and number of the 18S–5.8S–26S rDNA loci. The 5S rDNA loci had more heterogeneous profiles with one or two loci per haploid genome. Phylogenetic analysis suggested an ancient duplication event of the 5S rDNA loci and more recent post‐speciation translocation and deletion events. These genome restructurings are estimated to have occurred approximately 13.98 Mya in the middle Miocene, after Lepismium and Rhipsalis diverged. The ancestor of Lepismium may have had a similar karyotype to L. lumbricoides and the Rhipsalis spp. (i.e. one 5S locus on chromosome 2). Both genera hypothetically originated in the yungas (north‐eastern Argentina and southern Bolivia), but diversification of the Lepismium crown group probably originated from populations with duplicated 5S loci in the parana forests of south‐eastern Brazil (8.70 Mya in the late Miocene). Two migration events between the yungas and parana forests were suggested to explain the extant distribution of Lepismium spp. These results make Lepismium a model system for the study of the complex chromosomal evolution in plants. © 2015 The Linnean Society of London, Botanical Journal of the Linnean Society, 2015, 177 , 263–277.     

The intriguing complexities of mammalian gene regulation: How to link enhancers to regulated genes. Are we there yet?

The information encoded in genomes supports the differentiation and function of the more than 200 unique cell types, which exist in various mammalian species. The major mechanism driving cellular differentiation and specification is differential gene expression regulation. Cis-acting enhancers and silencers appear to have key roles in regulating the expression of mammalian genes. However, these cis-acting elements are often located very far away from the regulated gene. Therefore, it is hard to find all of them and link them to the regulated gene. An intriguing and unresolved issue of the field is to identify all of the enhancers of a particular gene and link these short regulatory sequences to the genes they regulate and thus, reliably identify gene regulatory enhancer networks. Recent advances in molecular biological methods coupled with Next-Generation Sequencing (NGS) technologies have opened up new possibilities in this area of genomics. In this review we summarize the technological advances, bioinformatics challenges and the potential molecular mechanisms allowing the construction of enhancer networks operating in specific cell types and/or activated by various signals.