苹果遗传转化的研究进展

苹果的遗传转化技术通过分子手段改良苹果,有助于缩短其育种周期。最近十年,在该领域的研究取得很大进展,涉及到一些重要的苹果基因型及有用的外源基因。迄今,苹果的遗传转化主要采用农杆菌介导法,侵染与转化材料的再生是影响其转化效率的关键过程,了解其影响因素,寻找有利因素以提高转化效率是目前苹果遗传转化研究的重点。     

nptⅡ基因真菌表达载体的构建及在苹果炭疽叶枯病菌遗传转化中的应用

本研究旨在构建1个适用于苹果炭疽叶枯病菌(Glomerella cingulata)的遗传转化载体,为系统研究该病原菌基因的功能提供便利。通过基因工程及分子生物学技术,将三磷酸甘油醛脱氢酶(GAPDH)基因启动子Pgap和新霉素磷酸转移酶基因(nptⅡ)连结于质粒p Cambia0380中。构建的载体p Gapneo R1导入根癌农杆菌LBA4404后,通过农杆菌介导的转化技术(ATMT),成功将nptⅡ基因盒整合到苹果炭疽叶枯病菌基因组中。Southern blot分析结果表明,随机挑取的转化子T-DNA均以单拷贝插入到苹果炭疽叶枯病菌基因组中,表明该载体适合于苹果炭疽叶枯病菌的遗传转化。此外,该载体也可用于构建苹果炭疽叶枯病菌的目标基因的回补载体、超表达载体和荧光融合蛋白表达载体。     

花生遗传转化的主要方法和研究进展

花生遗传转化研究对于花生品种改良、新品种繁育具有重要意义。农杆菌介导的遗传转化法和基因枪法是花生遗传转化的主要方法。随着对花生研究的深入开展,花生的遗传转化技术也越来越成熟。介绍了农杆菌介导的遗传转化法和基因枪法在花生遗传转化研究中的应用现状及存在的问题。     

根癌农杆菌介导真菌遗传转化的研究及应用

根癌农杆菌介导转化法（Agrobacterium tumefaciens-mediated transformation,ATMT）具有转化效率高、遗传稳定、适用范围广等诸多优点,已成为真菌遗传转化研究中的强有力手段,在真菌基因资源开发、真菌性疾病研究和外源蛋白表达研究中发挥巨大作用。本文概述了根癌农杆菌转化法在真菌转化中的研究进展、技术优缺点、转化机制、实验方法和应用现状,着重介绍影响其转化效率的因素并对优化方法进行探讨,展望了该技术在真菌基因资源发掘、基因编辑等方面的应用前景,为今后真菌的遗传转化研究提供参考。     

植物的遗传转化及其应用(英文)

近年来,植物遗传转化研究有了长足的发展。已经达到能够通过简单的遗传控制手段研究具有新表现型的植物,甚至达到进入商业化的程度。这些手段包括植物生物学的主要研究技术以及植物组织培养和树种改良的一些实用方法。尽管采用农瘤杆菌和鸟枪法等技术的植物遗传转化系统已经得到了广泛的应用,但是在如何开发具有能够得到控制表达的转基因高产植物方面,在如何使所得到的转基因植物远离遗传危害等方面,目前的转化系统遇到了极大的技术挑战。已经提出了各种各样的方法用于将新基因稳定地导入120多种不同植物的核基因组。本文将讨论这些遗传转化系统所需的生物学要求和实际应用方面的需求、基因转化和转基因表达的研究策略、遗传转化植物的鉴定以及转基因植物与大众的认可。本文将分为七个部分加以讨论:一、导言;二 、基因转化到细胞里的方法;三、植物遗传转化策略;四、植物遗传转化的鉴定;五、植物遗传转化的实际应用;六、转基因植物与环境;七、未来植物遗传转化的需求与发展方向。     

叶绿体遗传转化的研究

叶绿体的遗传转化是近几年发展起来的新领域。本文主要介绍了叶绿体遗传转化的特点、基本原理和外源基因转化叶绿体的方法与技术;综述了国外在此方面的研究进展及最新成就,以及叶绿体遗传转化体系在基础研究和生物技术领域中的应用。     

苹果遗传转化的研究进展

苹果的遗传转化技术通过分子手段改良苹果,有助于缩短其育种周期.最近十年,在该领域的研究取得很大进展,涉及到一些重要的苹果基因型及有用的外源基因.迄今,苹果的遗传转化主要采用农杆菌介导法,侵染与转化材料的再生是影响其转化效率的关键过程,了解其影响因素,寻找有利因素以提高转化效率是目前苹果遗传转化研究的重点。 Abstract:Techniques of apple genetic transformation can improve apple trees and shorten the breeding cycle by molecular methods.In the last years,great progress has been made in this field,which involves a number of important apple genotypes developed.So far,apple genetic ransformation mainly adopts Agrobacterium-mediated technique,involving infection and transgenic tissue regeneration,which are important steps to affect the transformation efficiency.The initial work to the date is to know and to search for the factors which can increase the efficiency.     

转基因植物中外源基因的遗传学行为

１９８４年,首次利用农杆菌Ｔｉ质粒将外源基因导人烟草获得成功［１」,随后,转基因禾本科作物在水稻上也获得了成功［２,３］。随着各种遗传转化技术的创立与改进,近十几年来,在许多作物上都获得了转基因植株。植物遗传转化技术在基础研究和应用研究中的价值得到了很大体现。尤其是在应用研究上,植物遗传转化技术与常规的育种技术相比,它以超越种间隔离的特点吸引了广大的分子育种家投入到这方面的研究。迄今为止,许多有应用前景的基因已导入到双子叶植物和单子叶植物,并有少量转基因植物已释放到大田应用［４,５］。我们实验室…     

影响籼稻基因枪法遗传转化效果的几个因素的研究(简报)

基因枪转化技术在水稻的遗传转化上已被广泛地应用并获得显著的成效。与原生质体转化法相比较,基因枪法具有不受或少受基因型限制的优点且提高了转化效率,但对籼稻,仍有不少问题需要解决,转化系统尚须进一步完善。因此有必要对影响转化频率的因素进行深入的研究。我们在以barnase基因对籼稻的遗传转化以诱发工程雄性不育的研究中,特别注     

苹果主栽品种高效遗传转化系统的建立及其影响因子的研究

研究影响农杆菌介导的苹果主栽品种遗传转化的若干因子效应,建立起新乔纳金苹果简单、高效的遗传转化系统。外源基因向新乔纳金苹果细胞转移的效率明显高于皇家嗄拉和富士苹果。菌株ＥＨＡ１０５介导基因转移的能力比菌株ＬＢＡ４４０４明显高。用乙酰丁香酮、磷酸饥饿、低ｐＨ值等ｖｉｒ基因诱导因子处理菌株ＥＨＡ１０５的细胞,未能提高转化效率。叶片在菌液中的浸泡时间不仅影响基因转移效率,而且影响头孢霉素对外植体上农杆菌生长的抑制效果。共培养时,叶片远轴面与培养基接触比近轴面与培养基接触的转化效率高。     

Mapping of the apple scab-resistance gene Vb.

Apple scab, caused by the fungus Venturia inaequalis, is the major production constraint in temperate zones with humid springs. Normally, its control relies on frequent and regular fungicide applications. Because this control strategy has come under increasing criticism, major efforts are being directed toward the breeding of scab-resistant apple cultivars. Modern apple breeding programs include the use of molecular markers, making it possible to combine several different scab-resistance genes in 1 apple cultivar (pyramiding) and to speed up the breeding process. The apple scab-resistance gene Vb is derived from the Siberian crab apple 'Hansen's baccata #2', and is 1 of the 6 "historical" major apple scab-resistance genes (Vf, Va, Vr, Vbj, Vm, and Vb). Molecular markers have been published for all these genes, except Vr. In testcross experiments conducted in the 1960s, it was reported that Vb segregated independently from 3 other major resistance genes, including Vf. Recently, however, Vb and Vf have both been mapped on linkage group 1, a result that contrasts with the findings from former testcross experiments. In this study, simple sequence repeat (SSR) markers were used to identify the precise position of Vb in a cross of 'Golden Delicious' (vbvb) and 'Hansen's baccata #2' (Vbvb). A genome scanning approach, a fast method already used to map apple scab-resistance genes Vr2 and Vm, was used, and the Vb locus was identified on linkage group 12, between the SSR markers Hi02d05 and Hi07f01. This finding confirms the independent segregation of Vb from Vf. With the identification of SSR markers linked to Vb, another major apple scab-resistance gene has become available; breeders can use it to develop durable resistant cultivars with several different resistance genes.     

影响苹果离体叶片早期转化效率因素的研究

利用gus为报告基因,通过统计gus基因瞬时表达的GUS 位点数和形成的愈伤组织,快速检测外源基因是否导入植物细胞及转化效率,以及对苹果转化早期阶段的影响因素。结果表明,A281对苹果叶片的浸染率比LBA4404浸染率要高,转化效率要好;叶片近轴面接触培养基转化效率较好,显著高于远轴面;整叶划痕为最佳切割方式,有利于提高苹果叶片转化率;苹果基因型、菌液浓度和共培养天数对不同基因型苹果的转化效率影响很大。     

Polyphenol gene expression and changes in anthocyanins and polyphenols in the skin of ‘Braeburn’ apples after the autumn application of prohexadione-calcium

Prohexadione-calcium (Pro-Ca) transient inhibits 2-Oxoglutarate-dependent dioxygenases and causes significant changes in the flavonoid spectrum of apple. In the present study the influence of two autumn preharvest applications of Pro-Ca on the polyphenol metabolism in apple peel during the advanced maturation was investigated. Pro-Ca was sprayed in two doses, approximately five and 3 weeks before the technological maturity. Changes in the concentrations of hydroxycinnamic acids, dihydrochalcones, flavonols, flavanols and anthocyanins as well as their related gene expression and enzyme activities in the apple peel were monitored six times during the advanced maturation until the technological maturity of the fruits. To evaluate its influence on red coloration differences in the chromatic values a*, h° and L* between the treated and untreated apples were monitored. The parameters showed a temporary effect of Pro-Ca on the intensity of red coloration, which was not detected anymore at the technological maturity of apples. The application of Pro-Ca decreased the flavanone 3-hydroxylase activity and slightly inhibited activities of all the enzymes analyzed. Concomitantly, the concentrations of anthocyanins in the peel of the treated apples decreased, whereas the concentrations of hydroxycinnamic acids, dihydrochalcones and flavan 3-ols increased. Flavonol concentrations, however, remained unchanged. The expression of ANS, ANR, FGT and MYB10 was downregulated after the Pro-Ca treatment. The results indicate that the autumn application of Pro-Ca modulates the biosynthetic pathway resulting in distinct changes in the flavonoid composition in the apple peel of ‘Braeburn’ apples. However, the changes are temporary and are generally suspended during apple storage.     

Overexpression of MsDREB6.2 results in cytokinin‐deficient developmental phenotypes and enhances drought tolerance in transgenic apple plants

Dehydration‐responsive element binding factors (DREBs) play important roles in plant growth, development, and stress signaling pathways in model plants. However, little is known about the function of DREBs in apple (Malus × domestica), a widely cultivated crop that is frequently threatened by drought. We isolated a DREB gene from Malus sieversii (Ledeb.) Roem., MsDREB6.2, and investigated its functions using overexpression analysis and c himeric re pressor gene‐s ilencing t echnology (CRES‐T). We identified possible target genes of the protein encoded by MsDREB6.2 using electrophoretic mobility shift assays (EMSAs) and chromatin immunoprecipitation (ChIP). Overexpression of MsDREB6.2 increased the expression of a key cytokinin (CK) catabolism gene, MdCKX4a, which led to a significant reduction in endogenous CK levels, and caused a decrease in shoot:root ratio in transgenic apple plants. Overexpression of MsDREB6.2 resulted in a decrease in stomatal aperture and density and an increase in root hydraulic conductance (L₀), and thereby enhanced drought tolerance in transgenic plants. Furthermore, manipulating the level of MsDREB6.2 expression altered the expression of two aquaporin (AQP) genes. The effect of the two AQP genes on L₀ was further characterized using the AQP inhibitor HgCl₂. Based on these observations, we conclude that MsDREB6.2 enhances drought tolerance and that its function may be due, at least in part, to its influence on stomatal opening, root growth, and AQP expression. These results may have applications in apple rootstock breeding programs aimed at developing drought‐resistant apple varieties.     

入侵动物福寿螺内生纤维素酶特性及应用研究进展

纤维素酶高效降解纤维素生产单糖,在纺织、造纸、食品、饲料等行业有重要应用价值.近年来,动物源的纤维素酶展现出优良的降解能力,其应用受到广泛关注.软体动物福寿螺是入侵我国华南地区的恶性外来物种,已经对水稻生产和湿地生物多样性造成了严重危害.福寿螺对多种植物的强消化能力与其体内的内生纤维素酶有密切关系.本文聚焦于福寿螺组织...     

The development of a cisgenic apple plant

Cisgenesis represents a step toward a new generation of GM crops. The lack of selectable genes (e.g. antibiotic or herbicide resistance) in the final product and the fact that the inserted gene(s) derive from organisms sexually compatible with the target crop should rise less environmental concerns and increase consumer's acceptance. Here we report the generation of a cisgenic apple plant by inserting the endogenous apple scab resistance gene HcrVf2 under the control of its own regulatory sequences into the scab susceptible apple cultivar Gala. A previously developed method based on Agrobacterium-mediated transformation combined with a positive and negative selection system and a chemically inducible recombination machinery allowed the generation of apple cv. Gala carrying the scab resistance gene HcrVf2 under its native regulatory sequences and no foreign genes. Three cisgenic lines were chosen for detailed investigation and were shown to carry a single T-DNA insertion and express the target gene HcrVf2. This is the first report of the generation of a true cisgenic plant.     

Apple gene function and gene family database: an integrated bioinformatics database for apple research

The apple (Malus domestica) is one of the most economically important fruit crops in the world, due its importance to human nutrition and health. To analyze the function and evolution of different apple genes, we developed apple gene function and gene family database (AppleGFDB) for collecting, storing, arranging, and integrating functional genomics information of the apple. The AppleGFDB provides several layers of information about the apple genes, including nucleotide and protein sequences, chromosomal locations, gene structures, and any publications related to these annotations. To further analyze the functional genomics data of apple genes, the AppleGFDB was designed to enable users to easily retrieve information through a suite of interfaces, including gene ontology, protein domain and InterPro. In addition, the database provides tools for analyzing the expression profiles and microRNAs of the apple. Moreover, all of the analyzed and collected data can be downloaded from the database. The database can also be accessed using a convenient web server that supports a full-text search, a BLAST sequence search, and database browsing. Furthermore, to facilitate cooperation among apple researchers, AppleGFDB is presented in a user-interactive platform, which provides users with the opportunity to modify apple gene annotations and submit publication information for related genes. AppleGFDB is available at http://www.applegene.org or http://gfdb.sdau.edu.cn/.     

Development of sequence-characterized amplified regions (SCARs) from amplified fragment length polymorphism (AFLP) markers tightly linked to the Vf gene in apple.

Amplified fragment length polymorphism (AFLP) markers have become widely used in saturating the region of a gene of interest for the ultimate goal of map-based cloning of the gene or for marker-assisted selection. However, conversion of AFLP markers into restriction fragment length polymorphism (RFLP) or polymerase chain reaction (PCR)-based markers will greatly expand their usefulness in genetic applications. Previously, we have identified 15 AFLP markers tightly linked to the Vf gene conferring scab resistance in apple. In this study, we have successfully converted 11 of these AFLPs into sequence-characterized amplified region (SCAR) markers. Of the remaining four nonconverted AFLP markers, one, ET2MC8-1, has been found to be very short (83 base pairs) and is an A/T rich (90%) marker; a second, EA2MG11-1, has shown identical sequences between Malus floribunda 821 (the original source of the Vf gene) and scab-susceptible apple cultivars; while the other two, EA12MG16-1 and ET8MG1-1, have not been cloned. Using the 11 converted SCAR markers along with 5 previously identified SCAR markers, a high-resolution linkage map around the Vf gene has been constructed, and found to be consistent with its corresponding AFLP map. Three converted SCAR markers (ACS-3, -7, and -9) are inseparable from the Vf gene; whereas one (ACS-6) is located left of, and the remaining seven (ACS-1, -2, -4, -5, -8, -10, and -11) are located right of the Vf gene at genetic distances of 0.4 and 0.2 cM, respectively. A reliable and robust procedure for development of SCAR markers from AFLP markers is presented.