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遗传学的发展与遗传学教学改革诌议 总被引:11,自引:4,他引:11
本文概述了遗传学的最近发展及其对遗传学教学提出的新问题。针对面临的问题,从遗传学教学的目标、要求及几大分支的内容处理等方面的改革提出了作者的观点,根据教学与市场的关系提出教学改革的初步意见。Abstract:New questions are now put forward to genetics teaching by the advance of genetics recently,and summarized in this discussion. According to relation between market requirement and education,the author suggested tentative proposal of reforming genetics teaching and improving contents of main parts in genetics. 相似文献
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本文指出了“遗传与变异”一章的具体内容、语言结构、英文名词、插图表格等方面存在的问题,并提出了相应的修改建议。作者认为:内容具有科学性、语言通顺流畅、英文名词翻译准确、图表应用规范是对教材的基本要求。Abstract:Some problems of “heredity and variation”in the book Medical Biology are presented in this article.These problems involve in contents,languages,English vocabularies,illustrations and tables,therefore some revisions are suggested.The author feel that it is a general demand that contents are scientific;languages are fluent;English vocabularies are correct; illustrations and tables are standardized. 相似文献
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运用广义和狭义的定义模式,对Morgan定律中的几个基本概念做了新的注释,深入地分析了经典三点测交的使用条件,并找出了粗糙脉孢菌的经典三点测交中不相邻两点间的交换值(FC)与其重组值(FR)差的出处。Abstract:Using the model of broad and narrow way,the paper introduces a new approach in the explaining of a few basic concepts in the Morgan Law.The paper introduces a thorough inquiry into the applying condition of the three-factor crosses,and finds the source of the difference between the crossover frequency (FC) and recombination frequency (FR) of the non-adjacent factors in the three-factor crosses in Neurospora crassa. 相似文献
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本文介绍了一组新编的人群嗅阈测量实验。该实验既兼顾了培养学生进行人类群体遗传调查的基本方法与技能和调查当地人群的嗅觉相关基因频率与分布两方面,又兼顾了课堂实验与课外研究两方面,是实验教学改革中比较成功的一种类型。Abstract:This paper presents a group of new experiments on human olfactory threshold measurement.It is a successful educational reform in teaching of genetic experiment.It considered not only training students' skills in the research on population genetics and investigating local population's olfactory allelic frequency,but also class experiments and research out of the class. 相似文献
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哮喘的分子遗传学研究进展 总被引:2,自引:1,他引:2
哮喘病和易感症的遣传学病因是复杂的,现可通过候选基因和易感位点筛选技术来进行研究。本文综述了哮喘易感基因的研究进展,同时讨论了哮喘遗传学研究对哮喘临床的应用前景。Abstract:The genetics of asthma and atopy is complex,but can be approached by studies of both candidate genes and mapping of susceptibility loci.The progress in susceptibility genes for asthma and atopy is reviewed.New therapeutic approaches to asthma which are based on the study on asthma genetics for future are summarized. 相似文献
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两个基因座位的遗传平衡原理 总被引:1,自引:0,他引:1
由于许多教科书中关于连锁平衡的介绍,多是引用结论或是推导不太严谨,使学生在学习群体遗传学时对理解连锁平衡的原理感到困难。本文从遗传平衡的基本条件出发,通过较严谨的数学推导,介绍了两个基因座的连锁平衡条件、平衡过程等原理,供教师和学生在群体遗传学教学中参考。Abstract: Because linkage equilibrium is introduced by directly quoting the conclusions or imprecise mathematical reasoning in most of textbooks, many students are puzzled with the problem of linkage equilibrium when they learn population genetics. Based on the radical conditions of genetic equilibrium, the principle of linkage equilibrium condition and process, for two gene loci is introduced by precise mathematical reasoning. The article may provide reference to teachers and students in the teaching and learning of population genetics. 相似文献
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三氧化二砷(As2O3)对蚕豆根尖毒性效应的细胞遗传学研究 总被引:15,自引:1,他引:15
本文以蚕豆根尖为材料,研究不同浓度As2O3在不同的处理时间内对蚕豆胚根根尖的细胞遗传学毒性效应。结果表明:不同浓度的As2O3在不同处理时间内均能诱发较高的微核率和染色体畸变率,并能有效地积累中期分裂相,阻止其进入后期与末期。结论是As2O3对蚕豆根尖细胞具有明显的细胞遗传学毒性效应,并具有积累有丝分裂中期细胞的效应。Abstract:The cytogenetic toxic effects of different concentration of As2O3 within different time on the cell of Vicia Faba root tip were studied.The results indicate that the different concentrations of As2O3 can induce high frequency of micronucleus and chromosome aberration.Besides,it can accumulate the metaphases in mitosis efficiently and prevent the cells from continuing their cell cycle.It shows that As2O3 has marked cytogenetic toxic effect on the root tip cells of Vicia Faba,and effect of accumulating the metaphases in mitosis. 相似文献
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不定胚再生植株的染色体数目变异 总被引:13,自引:0,他引:13
本实验以甜瓜“小麦瓜”和“青皮绿肉”品种为试材,经不定胚诱导再生植株。分别调查了不同继代培养时间后形成再生植株的染色体数目,并将之与对照染色体数目相比较,发现通过诱导不定胚所得到的再生植株中存在着一定的变异,而且经过不同继代培养时间后,所得到的不定胚再生植株的变异程度不同,随着时间的增加,染色体数目的变异率从3.3%增加到30%,变异幅度也从2n=23~24增加到2n=13~48。从而得出结论:不定胚再生植株染色体数目变异程度随着培养时间的增加而增加;培养时间在1~2个月内所得到的不定胚再生植株的变异较少。此外,不定胚再生植株的染色体数目变异程度也因品种而异。Abstract:Chromosomal number of different of somatic embryos regenerated plants were investigated in melon variety “xiaomaigua” and “Qingpilurou”.Certain variations of chromosomal number were found among the regenerated plants compared with normal sample,and range of variation covered from 2n=23~24 to 2n=13~48 with the increase of generation,the rate from 3.3% to 30%.The results indicated that degree of variation in chromosomal number of somatic embryos regenerated melon plants increased with the time of culture,and those cultured in one to two months had the least variation.It was also found that degree of chromosomal number variations varied with melon varieties. 相似文献
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小麦体细胞无性系Glu-1基因突变体的遗传分析 总被引:4,自引:0,他引:4
对 Glu-1基因的Glu-Al和Glu-Bl位点都发生突变的1个小麦体细胞无性系后代的高分子量谷蛋白亚基组成进行的分析结果,进一步证实了体细胞无性系发生了基因突变, 且发现同源染色体的等位基因易发生相同突变,突变体多是纯合基因型。认为这是体细胞无性系变异稳定快的遗传根源。Abstract:Evidence for specific gene mutation has been obtained in our previous research by analyzing high-molecular-weight glutenin subunits(HMW-GS)controlled by Glu-1 gene in wheat somaclons.On the basis of the result,the present study detected in the offspring of a HMW-GS somaclone the mutants at both Glu-A1 and Glu-B1 loci.The occurrence of gene mutation in wheat somaclones was further proved.The results showed that a allele on homologous chromosomes often mutated identically.Genotype of this kind mutation migh be pure.Thie is considered to be genetic reason for quickly stabilizing of somaclonal variation. 相似文献
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染色体结构变异,会扰乱机体的固有平衡系统,影响生殖和发育。在本科遗传学教学中,如何进一步诠释导致机体平衡系统紊乱的机理,是教师常面临的教学难题。一些嵌合基因(chimeric gene)是染色体结构变异的产物,具有特异的生物功能,可能是致使固有平衡系统紊乱的原因之一,但很少见到在课堂或教科书中讲述与嵌合基因相关的内容。本文结合近年本团队对嵌合基因的研究成果及遗传学教学实践,以一个司法案例创设情境,引入嵌合基因实例,以激发学生的学习兴趣;进而通过对嵌合基因通性的梳理,辅助学生总结知识点,发展思维融汇力,从而拓展染色体畸变的教学,以期使学生对基因的变异及其功能有更深入的理解,提高遗传学教学效果。 相似文献
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对中国云南西部和西北部分布的腋花扭柄花Streptopus simplex的4个居群进行了细胞学研究。生长在云南西北香格里拉县(原中甸县)碧塔海和小中甸冷杉林中的腋花扭柄花两个居群的体细胞染色体数目为2n=2x=18,而生长在高黎贡山的福贡县片马和贡山县的灌丛中的植物体细胞染色体数目则为2n=2x=14。2n=14为腋花扭柄花一个新的染色体数目,x=7为扭柄花属一个新的染色体基数。香格里拉碧塔海和小中甸两个居群的核型公式分别为2n=4m+8sm+4st和2n=8m+2sm+6st,染色体逐渐变小;贡山和福贡片马两个居群的核型公式分别为2n=14=4m+10sm和2n=14=7m+7sm,其中第一对中部着丝粒的染色体显著大于其余染色体。由于x=8是扭柄花属最常见的染色体基数,因此可认为x=8是腋花扭柄花的染色体原始基数,x=7的数目是衍生的;x=7居群染色体的一条大染色体可能是由x=8的染色体的两条st型染色体的着丝粒发生了罗伯逊易位而来。 相似文献
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Irenice Gomes de Oliveira Ana Paula Moraes Erton Mendona de Almeida Felipe Nollet Medeiros de Assis Juliano S. Cabral Fabio de Barros Leonardo P. Felix 《Botanical journal of the Linnean Society. Linnean Society of London》2015,178(1):102-120
In this study, we analysed chromosome number variation and chromomycin A3/4′,6‐diamidino‐2‐phenylindole (CMA/DAPI) banding patterns in 48 species belonging to 12 genera of subtribe Pleurothallidinae (Orchidaceae) in order to understand the chromosome evolution based on recent phylogenetic hypotheses and taxonomic treatments. All species had small chromosomes, with numbers ranging from 2n = 20 in two Specklinia spp. to 2n = 80 in an unidentified Octomeria sp. In Acianthera, the most highly represented genus in this study, a great diversity of chromosome number and pattern of fluorescent bands was observed, showing heterochromatin accumulation in Acianthera section Sicariae subsection Pectinatae. Interspecific ascending and, mainly, descending dysploidy were the main mechanisms of chromosome number evolution in subtribe Pleurothallidinae. For Pleurothallidinae, x = 20 is suggested as the basic chromosome number, the same suggested for the related subtribe Laeliinae and for the whole tribe Epidendreae. The Brazilian species of the mega‐genus Stelis had chromosomes with small amounts of heterochromatin and chromosome numbers based on x2 = 16. These are generally divergent from those reported for Andean and Meso‐American species, but in agreement with the monophyletic hypothesis proposed for Stelis spp. with a Brazilian Atlantic distribution. © 2015 The Linnean Society of London, Botanical Journal of the Linnean Society, 2015, 178 , 102–120. 相似文献
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Rhubarb (Rheum rhaponticum L.) is a tetraploid (2n = 44) vegetable crop growing in Europe and North America. The results observed 44 chromosomes for both cultivars Timperly Early and PC49, but showing significant differences in DNA contents between them. Abnormal chromosome numbers (2n = 22 and 32) and chromosomal fragments were observed only in micropropagated plants of rhubarb PC49, suggesting somaclonal variation. The results provide further information on understanding morphological variation and increased disease susceptibility of micropropagated rhubarb PC49 in our previous investigation. 相似文献
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Luca Comai Kirk R Amundson Benny Ordoez Xin Zhao Guilherme Tomaz Braz Jiming Jiang Isabelle M Henry 《Genetics》2021,219(3)
Large-scale structural variations, such as chromosomal translocations, can have profound effects on fitness and phenotype, but are difficult to identify and characterize. Here, we describe a simple and effective method aimed at identifying translocations using only the dosage of sequence reads mapped on the reference genome. We binned reads on genomic segments sized according to sequencing coverage and identified instances when copy number segregated in populations. For each dosage-polymorphic 1 Mb bin, we tested independence, effectively an apparent linkage disequilibrium (LD), with other variable bins. In nine potato (Solanum tuberosum) dihaploid families translocations affecting pericentromeric regions were common and in two cases were due to genomic misassembly. In two populations, we found evidence for translocation affecting euchromatic arms. In cv. PI 310467, a nonreciprocal translocation between chromosomes (chr.) 7 and 8 resulted in a 5–3 copy number change affecting several Mb at the respective chromosome tips. In cv. “Alca Tarma,” the terminal arm of chr. 4 translocated to the tip of chr. 1. Using oligonucleotide-based fluorescent in situ hybridization painting probes (oligo-FISH), we tested and confirmed the predicted arrangement in PI 310467. In 192 natural accessions of Arabidopsis thaliana, dosage haplotypes tended to vary continuously and resulted in higher noise, while apparent LD between pericentromeric regions suggested the effect of repeats. This method, LD-CNV, should be useful in species where translocations are suspected because it tests linkage without the need for genotyping. 相似文献
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Wang Zhong-ren 《植物学报(英文版)》1986,28(5)
A morphological and cytological study of a population of Ophioglossum petiolatum Hook. from the vicinity of Kunming, Yunnan Province was carried out. The fronds of this species are very variabte in. either size or figure. The outlines of laminae of different plants vary from narrowly lanceolate to ovate or broadly ovate (length: breadth can be from 6:1 to 1:1). The apices of laminae range from taper-pointed to acute or blunt, and the bases of laminae from attenuate to cuneate or nearly truncate. In most cases, the spore mother cells of the species have 480 bivalents at pro-meta- phase I of meiosis. The spores produced after normal meiosis are seemingly available. It shows that the species is an octoploid and probably sexual In few plants, many univalents at metaphase I of meiosis have also been seen, but we have failed to count their exact chromosome numbers. However, it reveals that there is a second cytotype in the population. From the fact that O. petiolatum has the great morphological variability and approximately constant chromosome number in a single population, the ecological conditions may not be the main reason of morphological variations of the Species. The high level of polyploidy and probable inbreeding system, the subterranean gametophytes must be hard to outcross, may give it a great ability of genetic lead which increases the genetic heterogeneity. and morphological varibility of populations. The voucher specimens are deposited inthe Herbarium of our Institute (PE). I am grateful to Prof. W. M. Chu of Yunnan University for his helpful suggestion and discuss. 相似文献
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Joseph D. DiBattista 《Conservation Genetics》2008,9(1):141-156
Genetic variation is considered critical for allowing natural populations to adapt to their changing environment, and yet the effects of human disturbance on genetic variation in the wild are poorly understood. Different types of human disturbances may genetically impact natural populations in a predictable manner and so the aim of this study was to provide an overview of these changes using a quantitative literature review approach. I examined both allozyme and microsatellite estimates of genetic variation from peer-reviewed journals, using the mean number of alleles per locus and expected heterozygosity as standardized metrics. Populations within each study were categorized according to the type of human disturbance experienced (“hunting/harvest”, “habitat fragmentation”, or “pollution”), and taxon-specific, as well as time- and context-dependent disturbance effects were considered. I found that human disturbances are associated with weak, but consistent changes in neutral genetic variation within natural populations. The direction of change was dependent on the type of human disturbance experienced, with some forms of anthropogenic challenges consistently decreasing genetic variation from background patterns (e.g., habitat fragmentation), whereas others had no effect (e.g., hunting/harvest) or even slightly increased genetic variation (e.g., pollution). These same measures appeared sensitive to both the time of origin and duration of the disturbance as well. This suggests that the presence or absence, strength, type, as well as the spatial and temporal scale of human disturbance experienced may warrant careful consideration when conservation management plans are formulated for natural populations, with particular attention paid to the effects of habitat fragmentation. 相似文献
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