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1.
The identification and metabolism of GA9 and its metabolites in seed coats and shoots of pea,line G2 总被引:1,自引:0,他引:1
[3H]gibberellin A9 was applied to shoots or seed parts of G2 pea to produce radiolabeled metabolites. These were used as markers during purification for the recovery of endogenous GA9 and its naturally occurring metabolites. GA9 and its metabolites were purified by HPLC, derivatized and examined by GC-MS. Endogenous GA9, GA20, GA29 and GA51 were identified in pea shoots and seed coats. GA51-catabolite and GA29-catabolite were also detected in seed coats. GA70 was detected in seed coats following the application of 1 g of GA9. Applied [3H]GA9 was metabolized through both the 13-hydroxylation and 2-hydroxylation pathways. Labeled metabolites were tentatively identified on the basis of co-chromatography on HPLC with endogenous compounds identified by GC-MS. In shoots [3H]GA51 and [3H]GA51-catabolite were the predominant metabolites after 6 hrs, but by 24 hrs there was little of these metabolites remaining, while [3H]GA29-catabolite and an unidentified metabolite predominated. In seed coats [3H]GA51 was the initial product, later followed by [3H]GA51-catabolite and an unidentified metabolite (different from that in shoots), with lesser amounts of [3H]GA20, [3H]GA29 and [3H]GA29-catabolite. [3H]GA70 was a very minor product in both cases. [3H]GA9 was not metabolized by pea cotyledons.Edited by T.J. Gianfagna.Author for correspondence 相似文献
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汉防己甲素(汉甲)及克矽平(Polyvinylpyridine-N-Oxide,PVNO)是目前较为有效的抑制矽肺纤维化的药物。本文研究了其对胶原mRNA水平的影响.斑点杂交实验表明大鼠接尘60天和120天后α1(Ⅰ)及α1(Ⅲ)mRNA水平明显上升,经汉甲或克矽平治疗1个月或3个月后,胶原mRNA水平明显下降。原位杂交结果表明胶原mR-NA银颗粒与细胞性结节和增厚的肺泡壁的成纤维细胞分布重合。汉甲或克矽平治疗后银颗粒数下降。提示汉甲及克矽平对矽肺进程中的胶原基因表达增强有抑制作用。 相似文献
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外源钙调蛋白对植物细胞分裂增殖作用的研究 总被引:1,自引:0,他引:1
外源钙调蛋白(Calmodulin,CaM)对胡萝卜悬浮细胞增殖具明显促进作用,不同浓度CaM的促进程度不同,7ug/ml时促进作用最大。CaM抑制剂TFP(Trifluoper-azine)则明显抑制该悬浮细胞的增殖,TFP浓度越高则抑制作用越强。另外,外源CaM可以加快珍珠梅花粉第二次有丝分裂,改变生殖细胞有丝分裂各期花粉管的比例,说明外源CaM对植物体细胞和性细胞的增殖和分裂均有促进作用。 相似文献
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Zn是植物必需的微量元素,同时也是近年来造成环境污染的重金属元素之一.为了从基因表达水平揭示小麦Zn胁迫响应的分子机制,本研究利用抑制差减杂交(suppression subtractive hybridization,SSH)技术构建了Zn胁迫(0.5 mmol/L,1 mmol/L)下小麦的正反向SSH文库.从正反向文库中随机挑选阳性单克隆,并利用通用引物T7/Sp6对其进行验证. 结果显示,正反库中分别获得307和821个EST序列,其片段长度在200~1 000 bp之间,它们反映了Zn胁迫下特异响应的基因.利用BLASTn和BLASTx将这些EST序列进行比对分析,在正、反库中分别筛选出221和641个uniESTs,其中751个uniESTs被注释(包括正库中193个和反库中558个).这些序列的功能主要涉及信号转导、抗氧化防御、转录与翻译、物质运输、核糖体结构、能量代谢,以及一些功能未知的基因. 相似文献
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Protection of mice with a divalent tuberculosis DNA vaccine encoding antigens Ag85B and MPT64 总被引:5,自引:0,他引:5
Tuberculosis (TB) remains to be a major challenge tothe public health in the world. It is estimated that, through-out the world, 15 individuals are affected by TB and 6 ofthem die from it every minute [1]. Drug resistance andcoinfection with HIV, which ut… 相似文献
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Isolation and analyses of genes preferentially expressed during early cotton fiber development by subtractive PCR and cDNA array 总被引:29,自引:0,他引:29
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Ji SJ Lu YC Feng JX Wei G Li J Shi YH Fu Q Liu D Luo JC Zhu YX 《Nucleic acids research》2003,31(10):2534-2543
Cotton fibers are differentiated epidermal cells originating from the outer integuments of the ovule. To identify genes involved in cotton fiber elongation, we performed subtractive PCR using cDNA prepared from 10 days post anthesis (d.p.a.) wild-type cotton fiber as tester and cDNA from a fuzzless-lintless (fl) mutant as driver. We recovered 280 independent cDNA fragments including most of the previously published cotton fiber-related genes. cDNA macroarrays showed that 172 genes were significantly up-regulated in elongating cotton fibers as confirmed by in situ hybridization in representative cases. Twenty-nine cDNAs, including a putative vacuolar (H+)-ATPase catalytic subunit, a kinesin-like calmodulin binding protein, several arabinogalactan proteins and key enzymes involved in long chain fatty acid biosynthesis, accumulated to greater than 50-fold in 10 d.p.a. fiber cells when compared to that in 0 d.p.a. ovules. Various upstream pathways, such as auxin signal transduction, the MAPK pathway and profilin- and expansin-induced cell wall loosening, were also activated during the fast fiber elongation period. This report constitutes the first systematic analysis of genes involved in cotton fiber development. Our results suggest that a concerted mechanism involving multiple cellular pathways is responsible for cotton fiber elongation. 相似文献
7.
He ZB Cao YQ Yin YP Wang ZK Chen B Peng GX Xia YX 《Development, growth & differentiation》2006,48(7):439-445
In long germ embryos, all body segments are specified simultaneously during the blastoderm stage. In contrast, in short germ embryos, only the anterior segments are specified during the blastoderm stage, leaving the rest of the body plan to be specified later. The striking embryological differences between short and long germ segmentation imply fundamental differences in patterning at the molecular level. To gain insights into the segmentation mechanisms of short germ insects, we have investigated the role of the homologue of the Drosophila gap gene hunchback (hb) in a short germ insect Locusta migratoria manilensi by paternal RNA interference (RNAi). Phenotypes resulting from hb knockdown were categorized into three classes based on severity. In the most extreme case, embryos developed the most anterior structures only, including the labrum, antennae and eyes. The following conclusions were drawn: (i) L. migratoria manilensis hb (Lmm'hb) controls germ band morphogenesis and segmentation in the anterior region; (ii) Lmm'hb may function as a gap gene in a wide domain including the entire gnathum and thorax; and (iii) Lmm'hb is required for proper growth of the posterior germ band. These findings suggest a more extensive role for L. migratoria manilensis hunchback in anterior patterning than those described in Drosophila. 相似文献
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Senescence, a sequence of biochemical and physiological events, constitutes the final stage of development In higher plants and is modulated by a variety of environmental factors and intemal factors. PPF1 possesses an important biological function in plant development by controlling the Ca2 storage capacity within chloroplasts. Here we show that the expression of PPF1 might play a pivotal role in negatively regulating plant senescence as revealed by the regulation of overexpression and suppression of PPF1 on plant development. Moreover, TFL1, a key regulator in the floral repression pathway, was screened out as one of the downstream targets for PPF1 in the senescence-signaling pathway. Investigation of the senescence-related phenotypes in PPF1(-) tfl1-1 and PPF1( ) tfl1-1 double mutants confirmed and further highlighted the relation of PPF1 with TFL1 in tranegenic plants. The activation of TFL1 expression by PPF1 defines an important pathway possibly essential for the negative regulation of plant senescence in transgenic Arabidopsis. 相似文献
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