Nucleotide sequence of the gene coding for the major protein of hepatitis B virus surface antigen.

DNA extracted from hepatitis B virus Dane particles has been cloned in bacteria using a plasmid vector. A full-length clone has been examined by restriction endonuclease analysis, and the nucleotide sequence of an 892-base pair fragment from cloned hepatitis B viral DNA encoding the surface antigen gene is reported. The amino acid sequence deduced from the DNA indicates that the surface antigens is a protein consisting of 226 amino acids and with a molecular weight of 25,398. The portion of the gene coding for this protein apparently contains no intervening sequences.     

Three naturally occurring Penstemon hybrids

Three wild Penstemon hybrids are documented herein: Penstemon clevelandii × spectabilis, P. centranthifolius × spectabilis , and P. centranthifolius × eatonii . Each putative hybrid was compared to its respective parental species using manifold floral and vegetative characters for which the parents differed. For each hybrid hypothesis, characters were counted as being intermediate or not intermediate. There were significantly more intermediate characters in all 3 cases (one-sided sign tests, P Penstemon species evidently do hybridize naturally, and for nearly all characters the hybrids are consistent with the view that the parents differ largely by additive genetic effects.     

A model for determination of the expected numbers of chromosome alterations and break points]

The assumption that the expected number of chromosome break points is simple and directly proportional to the length of chromosomes is criticized. Translocations and inversions imply two dependent break points in relation to their distribution on the whole karyotype, that is why, this assumption should be modified. A model is presented which takes the dependence into account and which provides the formulas for the calculations of probabilities of binary rearrangements and of their respectives break points. We apply the model to the human karyotype.     

低成本MEMS磁力计校正方法研究

基于MIMU(magnetic and inertial measurement unit)的人体动作捕捉技术,每个测量单元在使用前,均需要对其磁力计进行校正.然而,一套人体动作捕捉系统具有7至十几个MIMU,因此缩短MIMU中磁力计校正的总时间是亟需解决的关键问题.磁力计校正可采用的旋转形式主要有两种,分别为八字旋转的校正方法和绕着各单轴旋转的校正方法.为了节省磁力计的校正时间并保证磁力计的校正精度,提出了一种优化的校正方法.即采用最小二乘法的椭球拟合方法,根据求得的椭球模型原点和半径均方根误差,确定最佳的旋转形式和旋转次数,以较快、较准确地校正磁力计.实验结果表明,绕各单轴各旋转1次的校正方法效果最佳.     

Differential effect of silybin on the Fe2+-ADP and t-butyl hydroperoxide-induced microsomal lipid peroxidation

We have observed a differential effect of silybin dihemisuccinate on rat liver microsomal oxygen consumption and on lipid peroxidation induced by NADPH-Fe2+-ADP and t-butyl hydroperoxide. These results are ascribed to the antioxidant properties of the flavonoid. The differences observed in the effect of the catalysts may be a consequence of the different capacity of silybin to act as a scavenger of free radicals formed by NADPH-Fe2+-ADP or t-butyl hydroperoxide.     

Endotoxin-induced acceleration of ovum transport in rabbits.

Salmonella enteritidis-Boivin endotoxin (1--20 microgram/kg) induced accelerated oviductal ovum transport in rabbits in a dose-related manner. Indomethacin prevented this effect. Levels of prostaglandin E and F in uterine vein blood increased following endotoxin injection.     

Effect of mecloqualone on the oxygen and glucose uptake by brain tissue in vitro

Resumen La mecloqualona inhibe in vitro, la respiración de cortes y homogenizados de cerebro, incrementando el consumo de glucosa; este último efecto no se produce cuando al medio de incubación se añaden 100 mM de potasio.     

Differential effect of silybin on the Fe2+-ADP and t-butyl hydroperoxide-induced microsomal lipid peroxidation

Summary We have observed a differential effect of silybin dihemisuccinate on rat liver microsonal oxygen consumption and on lipid peroxidation induced by NADPH-Fe²⁺-ADP and t-butyl hydroperoxide. These results are ascribed to the antioxidant properties of the flavonoid. The differences observed in the effect of the catalysts may be a consequence of the different capacity of silybin to act as a scavenger of free radicals formed by NADPH-Fe²⁺-ADP or t-butyl hydroperoxide.This research was supported in part by grant B-2019-8412 from Dirección de Investigación y Bibliotecas, Universidad de Chile.     

Generation of functional multipotent adult stem cells from GPR125+ germline progenitors

Adult mammalian testis is a source of pluripotent stem cells. However, the lack of specific surface markers has hampered identification and tracking of the unrecognized subset of germ cells that gives rise to multipotent cells. Although embryonic-like cells can be derived from adult testis cultures after only several weeks in vitro, it is not known whether adult self-renewing spermatogonia in long-term culture can generate such stem cells as well. Here, we show that highly proliferative adult spermatogonial progenitor cells (SPCs) can be efficiently obtained by cultivation on mitotically inactivated testicular feeders containing CD34+ stromal cells. SPCs exhibit testicular repopulating activity in vivo and maintain the ability in long-term culture to give rise to multipotent adult spermatogonial-derived stem cells (MASCs). Furthermore, both SPCs and MASCs express GPR125, an orphan adhesion-type G-protein-coupled receptor. In knock-in mice bearing a GPR125-beta-galactosidase (LacZ) fusion protein under control of the native Gpr125 promoter (GPR125-LacZ), expression in the testis was detected exclusively in spermatogonia and not in differentiated germ cells. Primary GPR125-LacZ SPC lines retained GPR125 expression, underwent clonal expansion, maintained the phenotype of germline stem cells, and reconstituted spermatogenesis in busulphan-treated mice. Long-term cultures of GPR125+ SPCs (GSPCs) also converted into GPR125+ MASC colonies. GPR125+ MASCs generated derivatives of the three germ layers and contributed to chimaeric embryos, with concomitant downregulation of GPR125 during differentiation into GPR125- cells. MASCs also differentiated into contractile cardiac tissue in vitro and formed functional blood vessels in vivo. Molecular bookmarking by GPR125 in the adult mouse and, ultimately, in the human testis could enrich for a population of SPCs for derivation of GPR125+ MASCs, which may be employed for genetic manipulation, tissue regeneration and revascularization of ischaemic organs.