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Gene Present (gene + present)
Selected AbstractsHuman liver stem cell-derived microvesicles accelerate hepatic regeneration in hepatectomized ratsJOURNAL OF CELLULAR AND MOLECULAR MEDICINE, Issue 6b 2010M. B. Herrera Abstract Several studies indicate that adult stem cells may improve the recovery from acute tissue injury. It has been suggested that they may contribute to tissue regeneration by the release of paracrine factors promoting proliferation of tissue resident cells. However, the factors involved remain unknown. In the present study we found that microvesicles (MVs) derived from human liver stem cells (HLSC) induced in vitro proliferation and apoptosis resistance of human and rat hepatocytes. These effects required internalization of MVs in the hepatocytes by an ,4 -integrin-dependent mechanism. However, MVs pre-treated with RNase, even if internalized, were unable to induce hepatocyte proliferation and apoptosis resistance, suggesting an RNA-dependent effect. Microarray analysis and quantitative RT-PCR demonstrated that MVs were shuttling a specific subset of cellular mRNA, such as mRNA associated in the control of transcription, translation, proliferation and apoptosis. When administered in vivo, MVs accelerated the morphological and functional recovery of liver in a model of 70% hepatectomy in rats. This effect was associated with increase in hepatocyte proliferation and was abolished by RNase pre-treatment of MVs. Using human AGO2, as a reporter gene present in MVs, we found the expression of human AGO2 mRNA and protein in the liver of hepatectomized rats treated with MVs. These data suggested a translation of the MV shuttled mRNA into hepatocytes of treated rats. In conclusion, these results suggest that MVs derived from HLSC may activate a proliferative program in remnant hepatocytes after hepatectomy by a horizontal transfer of specific mRNA subsets. [source] Double Oestrogen Receptor , and , Knockout Mice Reveal Differences in Neural Oestrogen-Mediated Progestin Receptor Induction and Female Sexual BehaviourJOURNAL OF NEUROENDOCRINOLOGY, Issue 10 2003A. E. Kudwa Abstract To test the hypothesis that oestrogen receptor , (ER,) and ER, act together to mediate the actions of oestrogen in the ventromedial hypothalamus (VMH), we used mice with single or double knockout mutations of the ER, and ER, genes. Ovariectomized mice were implanted with 17,-oestradiol and killed 5 days later. Oestradiol treatment promoted progestin receptor (PR)-immunoreactivity (-ir) in the VMH of all genotypes, but was maximal in brains of wild-type and ER,KO females. Analysis of specific VMH subregions revealed that PR-ir induction was limited to the caudal VMH in ER,KO and ER,,KO mice. In the rostral VMH, oestradiol only induced PR-ir in wild-type and ER,KO mice, and the number of PR-ir neurones in this region was greater in ER,KO than wild-type females. Next, we tested the ability of a dopamine agonist and progesterone to facilitate sexual behaviour in females lacking functional ER,, ER,, or both receptors. Ovariectomized mice were implanted with oestradiol, and tested for sexual behaviour three times after administration of the dopamine agonist, apomorphine, followed by two tests concurrent with progesterone treatment and a final test with just apomorphine treatment. ER,KO and ER,,KO females failed to display lordosis under any testing conditions, while ER,KO females exhibited lordosis behaviour equal to that of wild-type females. Our data show that a subpopulation of PR-ir neurones is induced by oestradiol in the caudal VMH of female mice lacking both ER, and ER, genes. We hypothesize that this action of oestradiol is either mediated by a novel ER or by the mutant portion of the AF2 subregion of the ER, gene present in ER,KO brain. However, despite the presence of PR in VMH, females lacking a functional ER, gene do not display sexual behaviour, via either ligand-dependent or -independent activation. [source] Development and primary genetic analysis of a fertility temperature-sensitive polima cytoplasmic male sterility restorer in Brassica napusPLANT BREEDING, Issue 3 2007Z. X. Fan Abstract Over the past decade, the polima cytoplasmic male sterility (pol CMS) three-line and two-line systems have been developed for the production of hybrid seed in Brassica napus oilseed rape in China. The discovery of the novel pol CMS restorer line FL-204 is described here. It restores male fertility of hybrid plants in the pol CMS system, but hybrid seed production can only be carried out under autumn sowing in Wuhan in south China under moderate temperatures at flowering. The restorer cannot be used as a male for hybrid seed production in northwestern China (Gansu) under spring sowing conditions, because there it is more or less male sterile due to high temperatures at flowering. Because of this behaviour, it is referred to as a fertility temperature-sensitive restorer (FTSR) in this paper. F2, BC1 as well as double haploid populations were constructed to determine the inheritance of fertility restoration of FL-204 in the autumn at Wuhan and under spring sowing conditions at Gansu, respectively. Deviations from Mendelian genetics were observed. It was hypothesized that the change of fertility was the result of the interaction between nuclear genes [restoring gene (Rf) and temperature-sensitive genes (ts)] and the cytoplasm. The Rf gene in FL-204 was incapable of restoring male fertility of pol CMS lines under spring sowing conditions at Gansu where it is inactivated by the recessive ts gene present in FL-204. However, the ts gene(s) could be non-functional under moderate temperature conditions at flowering at Wuhan which allows full expression of male fertility in FL-204. The recessive ts gene(s) can only be expressed in plants containing the pol sterile cytoplasm. A method for the utilization of the FTSR pol CMS restorer FL-204 for the production of hybrid seed in B. napus oilseed rape is proposed. [source] Combination of resistance tests and molecular tests to postulate the yellow rust resistance gene Yr17 in bread wheat linesPLANT BREEDING, Issue 6 2000O. Robert Abstract Yellow rust caused by Puccinia striiformis is a wheat disease of worldwide importance. The Yr17 resistance gene introgressed from Aegilops ventricosa was effective, in France, against all yellow rust isolates until 1998. The SC-Y15 marker is one of three molecular markers closely linked to Yr17. In this paper, results obtained are compared with the molecular marker SC-Y15 and with resistance tests performed at the seedling and adult plant stages on 31 lines from five populations derived from recurrent selection programmes. The resistance tests showed that Yr17 controlled the resistance in seven lines, but that others had additional resistance at the adult stage (18 lines). The molecular test corresponded well with the resistance test in most lines (98% of 156 plants tested), including individual plants that were resistant or susceptible in heterogeneous lines. It also indicated the presence of Yr17 in lines in which it could not be identified by the resistance test because of the presence of other genes. Three of the 156 plants tested appeared to have the gene Yr17 according to the resistance tests, but lacked the molecular marker. These could have resulted from breakage of the linkage, the number being consistent with the estimate of linkage already published. This indicated the need for a resistance test, at least in later stages of breeding programmes, if it is considered essential to have the Yr17 gene present. The use of the selected lines in breeding programmes is also discussed. [source] | ||||||||||