西藏与周边地区芥菜型油菜农艺性状比较研究

运用典范相关分析方法,对西藏及周边地区芥菜型油菜的产量性状、主茎性状、分枝性状、角果性状等4组性状间的典范相关关系进行了比较研究.结果表明:(1)所研究的18个性状中,西藏芥菜型油菜的平均数为周边地区芥菜型油菜的1.88倍,总体变异系数比周边省份芥菜型油菜高10.22％;(2)西藏芥菜型油菜单株产量主要取决于每株角果数和千粒重,而周边省份芥菜型油菜单株产量主要取决于每株有效角果数,中国周边国家芥菜型油菜单株产量主要取决于每株有效角果数和千粒重;(3)影响西藏芥菜型油菜产量性状最重要的因素是角果性状,其次是分枝性状和主茎性状,而影响周边省份和中国周边国家芥菜型油菜产量性状最重要的因素则是主茎性状,其次是分枝性状和角果性状.     

西藏野生芥菜型油菜种质资源的聚类分析

以植株高度、基部粗度、分枝部位、分枝总数、每株角果数等14个考种性状为指标,对西藏各地(市)搜集而来的27份野生芥菜型油菜进行了聚类分析。结果表明:1)当阈值为0.94时,将供试材料分为上生分枝型野生芥菜型油菜(G1)、下生分枝型野生芥菜型油菜(G2)和匀生分枝型野生芥菜型油菜(G3)三大类群;可以根据育种目标及当地的生态因子等选择不同的株型,从而达到稳产、丰产的目的;2)当阈值为0.61时,将材料分为SG1、SG2、SG3、SG4、SG5、SG6、SG7等个七亚类群;发现西藏野生芥菜型油菜种质资源在地理分布上的距离并不能确切反映其遗传上的差异,因此提出研究西藏的作物生长环境时,不应以行政区划为研究标准,应参考当地的区域小气候;3)各西藏野生芥菜型油菜种质资源分类群的考种性状差异明显,生物多样性丰富。     

芥菜型多室油菜与甘蓝型油菜的种间远缘杂交

通过对芥菜型多室油菜与甘蓝型油菜种间杂交 以下简写为芥×甘或甘×芥 的结实性、交配性以及不同甘蓝型油菜对交配性的影响等研究发现:芥、甘正反交形成的饱满种子数较少,其形成种子的能力弱,但是芥×甘与甘×芥杂交相比,芥×甘形成饱满种子的能力较强,受精能力以及杂种胚胎的发育能力也强,在授粉后的子房发育上二者无显著差异.所以,芥菜型多室油菜与甘蓝型油菜种间杂交创建新资源时宜采用芥×甘杂交方式;不同甘蓝型油菜品种与芥菜型多室油菜正反交的结角率、受精指数、结籽指数和可交配指数均不相同,但可交配指数的变异系数最大.因此,筛选可交配性强的甘蓝型基因型应着眼于可交配指数高的甘蓝型油菜亲本材料,根据本试验结果,芥菜型多室油菜与甘蓝型油菜93-221-1杂交形成的杂种胚具有较强的可发育性.     

芥菜型油菜种质资源研究进展

本文从收集保存、鉴定、研究、创新和利用5个方面介绍了芥菜型油菜种质资源研究进展。芥菜型油菜起源于亚洲,印度、中国收集的资源最多。芥菜型油菜可以分为中国-东欧类型和中国-印度类型2大类,每一类中均存在较大的遗传变异,许多具有优良性状的种质已经鉴定出来,并对其进行了生理学、遗传学研究。通过远缘杂交、诱变和遗传转化已创造出芥菜型油菜新种质。已鉴定、培育的芥菜型油菜优异种质资源在油菜育种上得到广泛利用。     

甘蓝型油菜和芥菜型油菜种间杂交研究

甘蓝型油菜与芥菜型油菜杂交研究结果表明,杂交结实力与杂交组合方式以及参与杂交的亲本材料有关,以芥菜型油菜作母本的杂交结实力高于以甘蓝型作母本的组合：芥×甘杂交组合的平均结实数／花为 ２．６４ 粒,而甘×芥杂交组合的平均结实数／花为 ０．１０ 粒。芥甘杂种一代形态特征和生育期介于双亲之间,甘芥杂种一代不表现整齐的中间类型,株间差异明显;总体来看,芥甘杂种一代与双亲回交的结实力（０．４０,０．２１）低于甘芥杂种一代与双亲回交的结实力（３．３０,１．７４）,无论是芥甘杂种一代还是甘芥杂种一代,用甘蓝型油菜作父本回交的结实力高于用芥菜型油菜作父本回交的结实力,但也有个别回交组合出现例外,不表现上述规律。 Ｂ Ｃ１ 代种子当年播种出苗率低（１８．５％ ）,群体株间性状差异明显,生育期极不一致。芥甘杂种一代与甘蓝型油菜亲本第二次回交,其平均结实数／花较回交一代提高 １．０８ 粒, Ｂ Ｃ２ 代种子当年播种出苗率仍较低,但较对应的 Ｂ Ｃ１ 代稍有提高,群体中出现趋回交父本性状但雄性育性彻底退化的植株。芥甘杂种一代自由授粉所得 Ｆ２ 群体是一个变异极为丰富的遗传群体。     

芥菜型油菜和白菜型油菜种间杂种遗传分析

种间杂交是一种拓宽栽培作物遗传基础和转移优良性状的重要手段,已经广泛地用于作物品质的改良。本研究通过芥菜型油菜（Brassica juncea L.）和白菜型油菜（Brassica rapa L.）种间杂交,将芥菜型油菜的有利性状转移到白菜型油菜中,创造新型白菜型油菜,以改良白菜型油菜的农艺性状、提高抗逆性和拓宽其遗传基础。研究结果表明：以芥菜型油菜作母本、白菜型油菜作父本的杂交组合较易获得杂交种子,杂种F1植株营养生长具有较明显的杂种优势,但花粉完全不育;以白菜型油菜回交获得的BC1植株间表型差异明显,平均花粉可染率为34.8%,介于 0~84%之间,群体自交不亲和;BC1F1和BC2群体变异广泛,出现自交亲和植株和黄籽植株,平均花粉可染率分别为79.7%和79.1%。     

芥菜型油菜和芥蓝种间杂种的获得及其性状表现

种间杂交是拓宽遗传种质资源,创制新物种、新材料的重要手段。利用芥菜型油菜和芥蓝种间杂交人工创制其种间杂种,并对其形态学、细胞学特点进行分析。结果表明:不同的杂交组合30 d后的子房残留数和获得幼胚数差异明显,杂交组合是影响种间杂交结子(幼胚)的重要因素;通过形态学鉴定出真杂种36份,均表现为较强的营养体杂种优势。真杂种减数分裂均为异常,在减数分裂后期具有不同程度的染色体丢失现象;无性系染色体数目部分为27条,部分为27~34条。真杂种花粉育性可染率在0~47.87%,自交结实率介于0~3.65%之间。     

我国芥菜型油菜品种遗传多样性初探

用ＲＡＰＤ技术对包括春、冬芥菜型采及国外品种在内的３６个芥菜型油菜品种的遗传多样性进行了分析。在扩增得到的１２８条ＤＮＡ带中,多态性ＤＮＡ片段达８８．２８％。分析表明：春 油菜间遗传差异较大,国内冬性芥菜型油菜地方种多样性水平较高,２５份冬性品种分属Ⅰ、Ⅱ和Ⅲ类群,而春性芥菜型 采地方种均归于Ⅳ类;印度的ＲＬＭ１９８与四川的珙县金黄油菜、澳大利亚品种与我国春油菜品种亲缘关系密切。     

西藏野生芥菜型油菜构件种群相互关系及其与气候因素的灰色关联度分析

以生物构件理论为基础,运用灰色关联分析技术对西藏野生芥菜型油菜种群构件结构与环境因子的关系进行了研究。结果表明:1)每株角果数、每角果粒数和粒重是产量构成的重要指标,随着每株角果数、每角果粒数和粒重的增大,西藏野生芥菜型油菜的产量明显增加,它们之间的构件因子关联度较大;2)主茎系统是西藏野生芥菜型油菜植株的基础,其间的关联性显示了西藏野生芥菜型油菜植株构件组成的整合作用;3)一级分枝长度、一级分枝角果数、二级分枝数、一级分枝粗度之间有较大的关联度,但与一级分枝发生高度关联度相对较小;4)研究的7个环境因子与西藏野生芥菜型油菜种群的生长关系均较密切,且温度是影响西藏野生芥菜型油菜分布和生命活动相对重要的环境因子,而降水为次要因子。     

芥菜型和甘蓝型油菜及其杂种后代种子硫甙组成差异的研究

用高效液相色谱技术分析了芥菜型油菜（Ｂｒａｓｓｉｃａ ｊｕｎｃｅａ）和甘蓝型油菜（Ｂｒａｓｓｉｃａ ｎａｐｕｓ）种间杂种后代及共亲本的硫甙组成。结果表明,与亲本农艺性状相似的后代,那么其硫甙组成与亲本亦相似。各后代中硫甙组成与亲本相比,虽发生了不同管理的变化,但都有倾向母体的趋势。芥菜型油菜烯丙基硫甙含量,２－羟基－３－丁烯基硫甙含量低,而甘蓝型油菜２－羟基３－丁烯基硫甙含量高,烯丙基硫甙含量最低     

Loss of C-genome-specific markers during transgene introgression from Brassica napus to wild Brassica juncea

Transgene flow from engineered Brassica napus to wild weed relatives could potentially have an environmental effect. To evaluate the introgression of transgenic B. napus into wild Brassica juncea, the hybrid F₁ and backcross progenies derived from B. juncea (genome constitution AABB) and transgenic B. napus (AACC) crosses were investigated. C-genome-specific simple sequence repeat (SSR) markers corresponding to linkage groups N11–N19 in B. napus were screened and used to estimate the marker frequency in hybrid F₁ and backcross progenies. C-genome-specific markers could be stably detected in hybrid F₁ and backcross BC₁ plants, but were only rarely found in the BC₂–BC₅ generations. For example, a specific SSR marker for linkage group N12 segregated in BC₂ generation but were completely lost in BC₃–BC₅, while a specific SSR marker of linkage group N15 segregated in BC₁, BC₂ and BC₃ generations and was absent in more advanced backcrossed generations (BC₄ and BC₅). The results indicate that a certain gene regions in Brassica napus plants are transmitted at a relatively lower frequency to wild relatives, and more rapidly disappeared in subsequent backcross generations. We propose that a foreign gene or transgene that is integrated in the C-chromosome of Brassica napus could reduce the risk of introgression in nature.     

不同品种芥菜对Cu胁迫响应的差异

采用水培法研究了不同品种芥菜对Cu胁迫响应的差异。结果表明:4μmol·L-1和8μmol·L-1Cu处理均抑制根和地上部生物量的积累,根受到的抑制程度大于地上部,敏感品种受到的抑制程度大于抗性品种。根中Cu积累量大于地上部,敏感品种根中Cu积累量大于抗性品种。8μmol·L-1Cu处理能明显诱导芥菜根中的MDA、Pro含量的增加及AsA含量的减少,APX、POD活性上升和GR活性下降,而不改变SOD活性。     

Phytoremediation of aspirin and tetracycline by Brassica juncea

With the increasing release of pharmaceutical drugs in the environment, research is in progress for investigating alternative methods for their remediation. Various studies have shown the phytoremediation potential of Brassica juncea for metals. The current study was aimed at evaluating the phytoremediation potential of B. juncea for two different pharmaceutical drugs i.e. aspirin and tetracycline in in-vitro conditions. The seeds of B. juncea were germinated and grown for a period of 28 and 24 days for aspirin and tetracycline, respectively. The study analyzed the remediation rate of B. juncea for the selected drugs in three different sets of varying concentration along with any phytotoxic effects exerted by the drugs on the seeds. Preliminary results showed that the average remediation rate of aspirin and tetracycline at the end of experiment was approximately 90% and 71%, respectively. As initial drug concentrations were increased in the media, the remediation rate also improved. However, at higher concentrations, the plants showed phytotoxicity as depicted by the decrease in shoot length of the germinated seeds. These preliminary results indicated that B. juncea could tolerate and remediate pharmaceutical drugs such as analgesics and antibiotics.     

Callus Formation and Morphogenesis of Cultured Mustard (Brassica juncea) Protoplasts

Protoplasts from mustard seedling cotyledons were suspended in Nitsch medium and cultured at 26℃ under low intensity illumination. When colonies were observed in the cultures, fresh medium (3% sucrose replaced mannitol) was added by equalvolume. When protoplasts developed into small callus the cultures were transfered to modified MS agar medium, in which some of them produced roots while an others gave rise to green spots. Shoot-differentiation experiment is in progress.     

Effect of Salinity on Zinc uptake by Brassica juncea

Salinity is a major worldwide problem that affects agricultural soils and limits the reclamation of contaminated sites. Despite the large number of research papers published about salt tolerance in Brassica juncea L., there are very few accounts concerning the influence of salinity on the uptake of trace metals. In this study, B. juncea plants divided through soil sets comprising 0, 900 and 1800 mg Zn kg^?1, were treated with solutions containing 0, 60 and 120 mmol L^?1 of NaCl, with the purpose of observing the effect of salt on Zn uptake, and some physiological responses throughout the 90 days experiment. Increasing concentrations of NaCl and Zn produced a decline in the ecophysiological and biochemical properties of the plants, with observable synergistic effects on parameters like shoot dry weight, leaf area, or photochemical efficiency. Nevertheless, plants treated with 60 mmol L^?1 of NaCl accumulated striking harvestable amounts of Zn per plant that largely exceed those reported for Thlaspi caerulescens. It was concluded that salinity could play an important role on the uptake of Zn by B. juncea. The potential mechanisms behind these results are discussed, as well as the implications for phytoremediation of Zn on saline and non-saline soils.     

Development of Plantlets from Leaf Protoplast Culture in Brassica juncea var. tsatsi

Protoplast of two mustard cultivars: Brassica juncea var. tsatsi cv. “Quxian Jiaoercai” and “Bangbangcai”, were isolated by enzymolysis from leaf grown in vitro. Protoplasts were suspended in liquid medium and semi-solidified medium with 0.35% low melting point agarose which formed a thin layer floating on the surface of the liquid medium. The first division appeared after 48h in the culture. One week after the original culture, a diluted medium with gradual dicrease of mannitol concentrations (6%→4%→zero) was then added to the culture three times respectively at one week's interval. In this culture method cell division and formation of microcalli were achieved. During the liquid culture of protoplasts, shaking at 20 rpm from time to time was beneficial in the formation of cell colonies and microcalli. Cell colonies developed into calli of approx 0.5—1mm in diameter one month after culture. The plating efficiency, which defined as the percentage of microcatli to numbers of protoplasts, was 0.2%—1%. Shoot regeneration occured when leaf protoplast-derived calli of “Quxian Jiaoercai” were transferred onto the modified MS medium supplemented with BAP 2.0mg/L, KT 1.0mg/L and NAA 0.2mg/L, and those of -'Bangbangcai" were transferred onto the modified MS medium supplemented with BAP 2.0mg/L. Individual shoot was rooted on a rooting medium supplemented with NAA 0.2 or 0.4 mg/L.     

A Pin gene families encoding components of auxin efflux carriers in Brassica juncea

Based on the sequence information of Arabidopsis PIN1, two cDNAs encoding PIN homologues from Brassica juncea, Bjpin2 and Bjpin3, were isolated through cDNA library screening. Bjpin2 and Bjpin3 encoded proteins containing 640 and 635 amino acid residues, respectively, which shared 97.5% identities with each other and were highly homologous to Arabidopsis PIN1, PIN2 and other putative PIN proteins. BJPIN2 and BjPIN3 had similar structures as AtPIN proteins. Northern blot analysis indicated that Bjpin2 was expressed in stem, leaf and floral tissues, while Bjpin3 was expressed predominantly in stem and hypocotyls. Two promoter fragments of pin genes, Bjpin-X and Bjpin-Z, were isolated by 'genome walking' technique using primers at 5'-end of pin cDNA. Promoter-gus fusion studies revealed the GUS activities driven by Bjpin-X were at internal side of xylem and petal; while those driven by Bjpin-Z were detected at leaf vein, epidermal cell and cortex of stem, vascular tissues and anther. Results of the pin gene     

A Pin gene families encoding components of auxin efflux carriers in Brassica juncea

Based on the sequence information of Arabidopsis PIN1, two cDNAs encoding PIN homologues fromBrassica juncea, Bjpin2 and Bjpin3, were isolated through cDNA library screening. Bjpin2 and Bjpin3encoded proteins containing 640 and 635 amino acid residues, respectively, which shared 97.5% identities witheach other and were highly homologous to Arabidopsis PIN1, PIN2 and other putative PIN proteins. BjPIN2and BjPIN3 had similar structures as AtPIN proteins. Northern blot analysis indicated that Bjpin2 wasexpressed in stem, leaf and floral tissues, while Bjpin3 was expressed predominantly in stem and hypocotyls.Two promoter fragments of pin genes, Bjpin-X and Bjpin-Z, were isolated by ‘genome walking‘ techniqueusing primers at 5‘-end of pin cDNA. Promoter-gus fusion studies revealed the GUS activities driven byBjpin-X were at internal side of xylem and petal; while those driven by Bjpin-Z were detected at leaf vein,epidermal cell and cortex of stem, vascular tissues and anther. Results of the pin genes with differentexpression patterns in B. juncea suggested the presence of a gene family.