Early Intervention of Gastrodin Improved Motor Learning in Diabetic Rats Through Ameliorating Vascular Dysfunction

Neurochemical Research - The mechanism of cognitive dysfunction in diabetes is still unclear. Recently, studies have shown that the cerebellum is involved in cognition. Furthermore,...     

生菜遗传转化体系的建立及转基因研究

以散叶生菜大速生(Lactuca sativavar.capatataL.)为试材,以MS为基本培养基,采用不同激素配比,确定生菜高效诱芽培养基为MS 1.5mg/L6-BA 0.2mg/LIAA;抗生素敏感性试验表明,筛选培养基中适宜的潮霉素选择压为20mg/L,抑菌剂羧苄青霉素的适宜质量浓度为300mg/L;通过根癌农杆菌介导的叶盘法将携带O型和A型口蹄疫抗原决定簇融合基因O21-O14-A21-HBcAg转入大速生散叶生菜,对部分抗性植株进行PCR和PCR-Southern杂交检测,证实目的基因已经成功整合到生菜基因组中。RT-PCR检测初步表明,O21-O14-A21-HBcAg基因可以在生菜中正常转录表达。     

Aggregation of pre-implantation embryos improves establishment of parthenogenetic stem cells and expression of imprinted genes

Parthenogenetic embryonic stem cells (PgES) might advance cell replacement therapies and provide a valuable in vitro model system to study the genomic imprinting. However, the differential potential of PgES cells was limited. It could result from relative low heterology of PgES cells compared with ES cells from fertilization (fES), which produce different expression of most imprinted genes. Here, we described the establishment of PgES cells by aggregating parthenogenetic embryos at the 8-cell stage (aPgES cells), which may increase heterozygy. We found that derivation of aPgES cells in association with an increased number of inner cell mass cells by aggregating was more efficient than that of PgES cells from a single parthenogenetic blastocyst. The aPgES cells have normal karyotype, stain positive for alkaline phosphatase, express high levels of ES cell markers and can differentiate into teratomas composed of the three germ layers. Moreover, compared with PgES cells, the more highly upregulated paternally expressed imprinted genes were observed in aPgES cells, the same change was not shown in aPg blastocysts. This suggested that the aggregation induced effect could modify the expression of paternally expressed imprinted genes. Our studies showed that aPgES cells, the expression of imprinted genes in which more closely resemble fES cells than PgES cells, would contribute to all organs and avoiding immuno-rejection, which may provide invaluable material for regeneration medicine.     

POPX2 phosphatase regulates cell polarity and centrosome placement

Proper centrosome positioning is critical for many cellular functions, such as cell migration and maintenance of polarity. During wound healing, fibroblasts orient their centrosomes such that they face the wound edge. The centrosome orientation determines the direction of cells’ migration so that they can close the wound effectively. In this study, we investigated the regulation of centrosome polarization and have identified the phosphatase POPX2 as an important regulator of centrosome orientation. We found that POPX2 inhibits centrosome centration, but not rearward nuclear movement, by regulating multiple proteins that function in centrosome positioning. High POPX2 levels result in reduced motility of the kinesin-2 motor, which, in turn, inhibits the transport of N-cadherin to the cell periphery and cell junctions. Loss of N-cadherin localization to the cell membrane affects the localization of focal adhesions and perturbs CDC42-Par6/PKCζ signaling. In addition, overexpression of POPX2 also results in a loss of Par3 localization to the cell periphery and reduced levels of LIC2 (dynein light intermediate chain 2), leading to defects in microtubule tethering and dynamics at cell-cell contacts. Therefore, POPX2 functions as a regulator of signaling pathways to modulate the positioning of centrosome in fibroblast during wound healing.     

内蒙古中东部草原区克氏针茅形态特征和RAPD遗传分化的相关性研究

以分布在内蒙古锡林郭勒盟东部草甸草原、中部典型草原和中西部荒漠化草原的4个克氏针茅种群为研究对象,采用形态学标记和RAPD分子标记相结合的方法进行遗传分化研究。结果表明：（1）无论是用形态学数据所得欧氏遗传距离矩阵还是用RAPD所得无偏差的Nei’s遗传距离矩阵,与种群分布的地理距离之间均不存在显著的相关关系,说明克氏针茅种群遗传分化受自然选择的影响。（2）种群之间存在显著的形态分化和遗传分化（p<0.05）。（3）对形态学数据所得欧氏遗传距离矩阵和RAPD所得Nei’s无偏差遗传距离矩阵进行Mantel检验所得结果不显著,表明对克氏针茅形态分化和遗传分化起主要作用的选择力是不完全相同的。     

rRNA genes are not fully activated in mouse somatic cell nuclear transfer embryos

The well known and most important function of nucleoli is ribosome biogenesis. However, the nucleolus showed delayed development and malfunction in somatic cell nuclear transfer (NT) embryos. Previous studies indicated that nearly half rRNA genes (rDNA) in somatic cells were inactive and not transcribed. We compared the rDNA methylation level, active nucleolar organizer region (NORs) numbers, nucleolar proteins (upstream binding factor (UBF), nucleophosmin (B23)) distribution, and nucleolar-related gene expression in three different donor cells and NT embryos. The results showed embryonic stem cells (ESCs) had the most active NORs and lowest rDNA methylation level (7.66 and 6.76%), whereas mouse embryonic fibroblasts (MEFs) were the opposite (4.70 and 22.57%). After the donor cells were injected into enucleated MII oocytes, cumulus cells and MEFs nuclei lost B23 and UBF signals in 20 min, whereas in ESC-NT embryos, B23 and UBF signals could still be detected at 60 min post-NT. The embryos derived from ESCs, cumulus cells, and MEFs showed the same trend in active NORs numbers (7.19 versus 6.68 versus 5.77, p < 0.05) and rDNA methylation levels (6.36 versus 9.67% versus 15.52%) at the 4-cell stage as that in donor cells. However, the MEF-NT embryos displayed low rRNA synthesis/processing potential at morula stage and had an obvious decrease in blastocyst developmental rate. The results presented clear evidences that the rDNA reprogramming efficiency in NT embryos was determined by the rDNA activity in donor cells from which they derived.     

内蒙古锡林郭勒高原大针茅种群分株构件数量性状的地理变异研究

采用单因素方差分析、变异组分分析和分形几何学的原理和方法,对内蒙古锡林郭勒盟不同气候条件下的三个大针茅种群分株构件数量性状进行了研究,并结合它们所在生境特点对所得结果进行了分析。结果显示：（1）整个生长季内,不同种群大针茅营养枝高度的生长模式不同;营养枝高度和生殖枝高度在种群间差异显著,且多数变异存在于种群之间;（2）在不同生长期内,大针茅种群地上部干重与植株高度之间存在显著的分形关系;在无强度干扰的情况下,大针茅种群营养枝分形维数的大小与大针茅营养枝地上部干重的累积程度是一致的;但在长期严重干旱条件下,分形维数值表现为快速增加;（3）整个生长季内,同一生境条件下大针茅种群营养枝地上部干重与植株高度之间也存在显著的分形关系,且不同样地间分形维数值差异显著。不同生境条件下大针茅种群分株构件数量性状的差异是对所在生境长期适应、自然选择的结果。     

Cre/loxP介导的伤寒杆菌染色体上插入基因的切除

来源于P1噬菌体的位点专一性重组系统loxP/Cre,已成为一种新的DNA操作的有用工具,在体内外都获得了成功的应用.为了将四环素诱导表达系统引入减毒伤寒杆菌CVD908株中,tetR-loxP-neo串联基因已通过同源重组被定位插入在CVD908株的△aroC位点中.构建一Cre酶表达受启动子P_LtetO-1控制的自杀质粒pJG9/Cre,以切除CVD908株△aroC中同向loxP序列之间的neo基因.质粒pJG9/Cre电转化入菌中,加入去水四环素诱导Cre酶表达,通过重组切除neo基因,再通过自杀质粒上SacB基因的启动,使质粒清除出菌细胞.抗生素鉴定和PCR扩增都证明,CVD908株△aroC位点中的neo基因被成功切除.