表达序列标签（ESTs）及其应用

表达序列标签(ESTs)是指从(ESTcDNA文库中随机挑取克隆并对其3’或5’端进行单轮自动测序所获得的短cDNA库列，一般长度为300～500bp。要有效获取ESTs，必须对cDNA文库进行预处理，处理方法有衰减杂交法、均一化法和差异显示法。在dbEST中收录了大量各种生物的ESTs。ESTs广泛应用于鉴定基因、发现新基因、电子克隆、构建遗传学图谱、制备DNA芯片、分子标记、研究基因的差异表达及检验病原微生物等方面。     

AFLP标记在大白菜遗传育种中的应用

AFLP标记是一种新的DNA分子标记技术。对AFLP标记的基本原理、技术流程和关键技术做了简要介绍,从亲缘关系与遗传多样性分析、遗传图谱的构建、特定性状的连锁标记、品种纯度鉴定与QTL分析等方面概述了AFLP标记在大白菜遗传育种中的应用进展,并对其应用前景进行了展望。     

牛遗传图谱的研究进展

20世纪90年代以来,牛遗传图谱发展非常迅速。到目前为止,已经公布了几个版本的遗传图谱。在图谱上DNA标记不断增加,标记间隔越来越小,但是目前图谱还是存在着标记密度不均匀等问题。随着牛基因组计划的完成,基因组学和QTL定位的发展,尤其是表达序列标签（EST）在图谱构建中的应用,牛的遗传图谱将更加完善,为重要经济性状的基因定位和基因克隆奠定了基础。     

黄鳍棘鲷标志放流群体的规格适宜性评价

合理选取标志放流鱼的规格是成功监测放流鱼类动态及评估增殖效果的关键步骤。本研究以黄鳍棘鲷为对象,通过2个实验评价标志鱼的适宜规格。实验1对比了4种体长的黄鳍棘鲷(平均体长5、7、11和14 cm)作T型标志后其生长、存活和标志保留情况,并利用逻辑斯蒂回归模型分别分析标志鱼存活率和标志保留率的规格特异性;实验2模拟了不同混合比例下2种体长黄鳍棘鲷标志鱼与不标志鱼的捕捞情况,并利用重抽样方法对捕捞结果作计算机重抽样,分析2种鱼能否充分混合以及标志鱼的规格、比例对捕捞结果的影响。结果显示:(1)7、11和14 cm标志组的特定生长率与对照组无显著差异;(2)标志鱼的存活率随体长的增加而增加(5 cm标志组的鱼在标志后7 d内全部死亡,7、11和14 cm标志组的存活率分别为77.5%、92.5%和100.0%)。标志鱼的存活率与初始体长的逻辑斯蒂回归关系式为P=exp(0.099X-6.900)/[1+exp(0.099X-6.900)];(3)各组的标志保留率较高(7、11和14 cm标志组的标志保留率分别为97.5%、100.0%和100.0%),但与体长无明显关系;(4)模拟捕捞结果与计算机重抽样结果无显著差异,二者均不受鱼体规格的影响,但受标志鱼比例的影响极显著,标志鱼比例越高,其捕获率也越高。综上,建议今后采用T型标志方法开展增殖放流品种(如黄鳍棘鲷)的相关研究时,应综合考虑成本和可接受的误差范围以选择符合研究目的的标志鱼规格,若需标志鱼的存活率高于50.0%,则体长至少为7 cm,高于75.0%则体长至少为8 cm,高于95.0%则体长至少为10 cm。此外,在成本允许的条件下,建议尽可能增加放流鱼类中标志鱼的比例以提高增殖效果评估的代表性,而具体适宜的比例值得深入研究。     

SRAP分子标记在棉花遗传育种中的应用

SRAP(Sequence-related Amplified Polymorphism)是1项基于PCR技术的新型分子标记技术,具有操作简便、稳定、高效、高共显性、便于测序目标片断等特点。介绍了SRAP分子标记技术的原理和特点,并综述其在棉花遗传连锁图谱的构建、遗传多样性分析、基因定位等方面的研究进展和应用前景。     

农学专升本《遗传学》课程教学改革探究

基于专科和本科培养目标的不同,针对专升本农学专业遗传学教学现状及存在的相关问题进行分析,提出了围绕遗传学课程体系,统筹兼顾,优化教学内容,改革教学方法,加强实验教学等方面,提高学生学习兴趣,增强知识综合应用能力,以适应现代本科教育的需要。     

Genetics of neotropical fish: from chromosomes to populations

The Neotropical freshwater fish fauna is very rich—according to the most recent catalogue 71 families and 4,475 species have been described. However, only a small amount of general information is available on the composition of Neotropical marine fishes. In Brazil, 1,298 marine species have been recorded. General analysis of available cytogenetic and population genetic data clearly indicates research has been mainly concentrated on freshwater fishes. Thus, today, cytogenetic information is available for 475 species of Characiformes, 318 species of Siluriformes, 48 species of Gymnotiformes, 199 freshwater species that do not belong to the superorder Ostariophysi, and only 109 species of marine fishes. For the species studied, only about 6% have sex chromosomes and about 5% have supernumerary or B chromosomes. A review of the cytogenetic studies shows that these data have provided valuable information about the relationships between fish groups, the occurrence of cryptic species and species complexes, the mechanism of sex determination and sex chromosome evolution, the distribution of nucleolus organizer regions, the existence supernumerary chromosomes, and the relationship between polyploidy and evolution. In relation to populations in Neotropical marine waters, the studies have shown the presence of cryptic species, which has important implications for fishery management. Different levels of genetic structuring can be found among Neotropical freshwater migratory fish species. This raises important implications for fish population genetic diversity and consequently its sustainable utilization in inland fisheries and aquaculture, specifically for conservation of ichthyo-diversity and survival.     

香菇遗传研究和菌种选育的现状及发展

本文通过回顾香菇菌种选育的四个历史阶段,阐述了在原生质体技术基础上发展起来的育种技术,全面分析了国内外遗传研究和菌种选育的现状,指出我国香菇生产中存在的主要问题是菌种退化、菌种混乱和菌种选育滞后,剖析了解决菌种问题的技术方法,提出了香菇遗传研究和菌种选育的方向。     

杨树抗黑斑病相关基因表达谱分析

利用黑斑病的高抗无性系美洲黑杨I-69及黑斑病的高感无性系欧美杨I-45为材料建立的2个cDNA文库,随机挑取cDNA克隆进行5'端EST序列测序,共获得有效序列20 023条.序列经聚类分析和拼接后,共获得10 816个Unigene,其中包括3 734个Contig,7 082个独立的Singleton.被注释的8 853个具有同源性匹配序列基因中,按照GO的分子功能、生物过程和细胞组分3个不同分类角度进行分类.在具有功能注释的8 853个Unigene中,选出330个与完成全基因组测序的毛果杨序列进行BLAST分析,结果发现有177个抗病相关候选基因出现在282个Unigene中,其中135个分布于杨树的18个不同连锁群上,其他42个基因位于还没定位的scaffolds上.所测定的这些EST序列为后期在基因组水平上研究杨树黑斑病的水平抗性遗传机制及进一步的相关基因发现奠定基础.

Abstract：

In an attempt to elucidate the molecular mechanism for resistance of black spot disease in poplar,gene expression profiles in leaves of Populus deltoides'Lus'(I-69/55)and P.euramericana'I-45/51',which were inoculated with the pathogen Marssonina brunnea f.sp.brunnea,were analyzed based on expressed sequence tags (ESTs).A total of 20 023 valid ESTs from the 5'terminal ends derived from corresponding cDNA libraries of the two poplar species were sequenced.Cluster analysis of the 20 023 sequences yielded 10 816 tentative unigenes,including 3 734 contigs and 7 082 singletons.All tentative unigenes were classified by Gene Ontology functional categories.To find resistance-associated candidate genes and locate them on poplar genome,330 unigenes was chosen from 8 853 annotated tentative unigenes,and their BLAST alignment was conducted with Populus trichocarpa assembly,1 77 related candidate resistant genes were found,and they presented in 282 unigenes.Among these genes,there were 1 35 genes located on 18 different linkage groups of poplar genome,and 42 genes located on the different scaffolds.This study supplied a resource of candidate genes for further exploring the genetic mechanism for the host horizontal resistance to the pathogen Marssonina brunnea at the whole genome range,and provided important information for further gene discovery.