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1.
Marina Cinco 《FEMS microbiology letters》1992,92(1):15-18
This investigation was undertaken to select antigenic variants of a Borrelia burgdorferi strain in vitro. The original strain BITS was cultivated in BSK medium supplemented with increasing concentrations of homologous hyperimmune serum raised in rabbits. After a few serial passages starting from a subinhibitory serum dilution of 1:800 in BSK up to 1:200, a variant named BITSv was obtained; it grew abundantly like the control culture in the presence of hyperimmune serum. Analysis of the antigenic pattern of the original and derived variants by Western blotting revealed that BITSv, compared to the original strain BITS, had lost the reactivity with the immune serum at the level of the oligosaccharide moiety. These experiments, designed to mimic the possible action of antibodies that arise during a Borrelia infection, suggest that lipopolysaccharides are surface located and that they play a role in the integrity of the outer membrane during the multiplication of Borrelia burgdorferi. 相似文献
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3.
J. Ruiz-Herrera J. P. Martinez M. Casanova M. L. Gil R. Sentandreu 《Archives of microbiology》1987,149(2):156-162
Cells from the slime variant of Neurospora crassa were broken in isotonic conditions by use of triethanolamine buffer plus EDTA. After removal of large membranous structures by low-speed centrifugation, chitosomes and secretory vesicles were separated by means of gel filtration, precipitation of membranous contaminants with Concanavalin A, and centrifugation in sucrose or glycerol gradients. Polypeptidic composition of fractions enriched in secretory vesicles or chitosomes was found to be distinct. By these criteria we concluded that chitosomes and secretory vesicles represent different populations of microvesicles. Both microvesicular populations appeared free of endoplasmic reticulum and vacuolar contaminants as demonstrated by determination of appropriate enzymatic markers.Abbreviations ER
Endoplasmic reticulum
- UDP-GlcNAc
uridine-5-diphosphate N-acetyl glucosamine
- GlcNAc
N-acetyl glucosamine
- SDS
sodium dodecyl sulfate
- PMSF
phenyl methyl sulfonyl fluoride
- EDTA
ethylene diamino tetraacetic acid
Investigador Nacional de Mexico. On leave from the Centro de Investigacion y Estudios Avanzados (IPN), and the Universidad de Guanajuato, Gto., Mexico 相似文献
4.
A human histone H2B.1 variant gene, located on chromosome 1, utilizes alternative 3' end processing.
D Collart P L Romain K Huebner S Pockwinse S Pilapil L A Cannizzaro J B Lian C M Croce J L Stein G S Stein 《Journal of cellular biochemistry》1992,50(4):374-385
A variant human H2B histone gene (GL105), previously shown to encode a 2300 nt replication independent mRNA, has been cloned. We demonstrate this gene expresses alternative mRNAs regulated differentially during the HeLa S3 cell cycle. The H2B-Gl105 gene encodes both a 500 nt cell cycle dependent mRNA and a 2300 nt constitutively expressed mRNA. The 3' end of the cell cycle regulated mRNA terminates immediately following the region of hyphenated dyad symmetry typical of most histone mRNAs, whereas the constitutively expressed mRNA has a 1798 nt non-translated trailer that contains the same region of hyphenated dyad symmetry but is polyadenylated. The cap site for the H2B-GL105 mRNAs is located 42 nt upstream of the protein coding region. The H2B-GL105 histone gene was localized to chromosome region 1q21-1q23 by chromosomal in situ hybridization and by analysis of rodent-human somatic cell hybrids using an H2B-GL105 specific probe. The H2B-GL105 gene is paired with a functional H2A histone gene and this H2A/H2B gene pair is separated by a bidirectionally transcribed intergenic promoter region containing consensus TATA and CCAAT boxes and an OTF-1 element. These results demonstrate that cell cycle regulated and constitutively expressed histone mRNAs can be encoded by the same gene, and indicate that alternative 3' end processing may be an important mechanism for regulation of histone mRNA. Such control further increases the versatility by which cells can modulate the synthesis of replication-dependent as well as variant histone proteins during the cell cycle and at the onset of differentiation. 相似文献
5.
O-Methylthreonine (OMT) inhibits the growth of plated Rosa cells (ID506·10-6M). Isoleucine is able to reverse efficiently and specifically this OMT toxicity. From OMT-resistant colonies occurring at a frequency of 1.58·10-7 variants per cell plated at 10-4M OMT, the variant strains OMTR-1 and OMTR-2 were isolated, cloned via protoplasts and characterized. Both variants were ten times more resistant to OMT than the wildtype and were cross-resistant to another isoleucine analog, dl-4-thiaisoleucine. The resistant variants retained their resistance after storage for three years in liquid nitrogen. Both resistant strains were stable for several months when subcultured in the absence of OMT although it was shown in a reconstitution experiment that wildtype cells overgrow OMTR-2 variant cells if co-cultivated for many passages in drug-free medium. One case of instability was observed upon long-term subculturing in drug-free medium: the strain OMTR-1D* partially lost phenotypic properties. Resistance to OMT was followed qualitatively by a new method based on inhibition-zone formation in cell suspensions plated in agar medium. The OMT-resistant variants showed a reduction in sensitivity of the enzyme l-threonine deaminase to feedback inhibition by isoleucine, a decreased stability of l-threonine deaminase when stored at-18°C or incubated at +55°C and a two- to threefold increase of the free isoleucine pool within the cells. The genetical events and the biochemical mechanisms which might lead to the observed stable and biochemically defined character are discussed with particular reference to the high ploidy level of the Rosa cell line.Abbreviations OMT
l-O-methylthreonine
- TD
l-threonine deaminase 相似文献
6.
长非编码RNA(long non-coding RNAs, lncRNAs)在肿瘤发生、发展进程中承担重要角色,是近年来的研究热点之一。大量研究表明,浆细胞瘤变异易位基因1(plasmacytoma variant translocation 1, PVT1)可通过多种分子机制参与调控消化系统肿瘤的增殖凋亡、迁移侵袭、细胞自噬、血管生成、多药耐药及肿瘤代谢等过程,从而发挥致癌作用。本文主要就PVT1在消化系统肿瘤中的表达水平变化,及其与临床病理特征和预后的关系,以及PVT1对消化系统肿瘤的致癌作用机制和多药耐药机制等研究进展作一综述。 相似文献
7.
Dominique Le Grand Michel Solsona Renate Rosengarten francois Poumarat 《FEMS microbiology letters》1996,144(2-3):267-275
Abstract The variability of predominant Mycoplasma bovis surface antigens in the presence of specific immune pressure was analyzed in an in vitro assay to determine if M. bovis could escape immune destruction. We have shown that serum antibodies from immunized or experimentally infected calves and monoclonal antibodies which specifically react with previously characterized or as yet undefined major M. bovis membrane surface proteins cause repression of expression or shortening of the target protein, or induce switching to expression of an antigenically distinct variant protein. We have further demonstrated that removal of the inducing antibody results in reversion to the original phenotype. These results suggest that the level of expression and the length of M. bovis surface antigens in the host is modulated by cognate antibodies. According to the surface antigenic variation systems, random selection of preexisting variants resistant to antibody-mediated inhibition or direct regulation of gene expression may be means by which this organism evades host immune defences. 相似文献
8.
游离氨基酸组分分析表明,水稻培养细胞中谷氨酸和丙氨酸含量很高,占氨基酸总量的40%。高脯氨酸愈伤组织变异体总游离氨基酸含量比原型高45.5%,其中脯氨酸增加最多,其次是雨氨酸和谷氨酸。当NaCl100mmol/L处理时变异体和原型的总氨基酸都增加,而变异体的增量约为原型增量的3倍。蛋白水解氨基酸组分中变异体和原型各氨基酸的相对含量无大差异。蛋白质双向电泳表明,高脯氨酸变异体的蛋白组分发生变化,明显比原型多4个蛋白点。在NaCl100mmol/L处理下原型亦产生53.3kD蛋白,变异体中该蛋白的含量变得更多。盐胁迫下变异体和原型的蛋白质组分变化的差异十分显著,主要表现在蛋白质等电点的变化不同。 相似文献
9.
芦苇耐盐变异植株及其细胞学鉴定 总被引:5,自引:0,他引:5
用甲基磺酸乙酯(EMS)处理芦苇(Phragm itescom m unis Trin.)胚性愈伤组织。从处理后的愈伤组织诱导获得芦苇耐盐变异植株R5002-12。变异植株能在含有1% NaCl的MS培养基上生长。细胞学检查变异植株是混倍体,染色体数目变异范围在100至33 之间。分蘖植株具有相似的形态学及染色体变异特性 相似文献