普通小麦与长穗偃麦草杂种及其衍生材料的细胞遗传学特性

对十倍体长穗偃麦草(Thinopyrum ponticum)与普通小麦杂交F1及其与普通小麦回交BC1F1的形态学和细胞学特性进行了分析。结果表明,长穗偃麦草与普通小麦‘兰考矮早八’衍生F1(‘兰考小偃麦’)的根尖细胞染色体数为56条;花粉母细胞减数分裂中期Ⅰ染色体构型平均值为19.81Ⅰ+15.78Ⅱ+0.75Ⅲ+0.59Ⅳ;基因组荧光原位杂交(GISH)显示,兰考小偃麦中含有35条完整的长穗偃麦草和21条小麦染色体。‘兰考小偃麦’/‘科育818’和‘兰考小偃麦’/‘Cp02-3-5-5’杂交F1的根尖细胞染色体数及其所遗传的长穗偃麦草染色体数分别为50~52和16~22条,且存在染色体易位;花粉母细胞减数分裂中期Ⅰ平均染色体构型为14.54Ⅰ+17.40Ⅱ+0.55Ⅲ+0.14Ⅳ,平均49.4%的细胞出现多价体(三价体或四价体)。这些材料为创造小麦-长穗偃麦草新种质奠定了基础。     

八倍体小偃麦染色体组分析

本文对普通小麦与长穗偃麦草(Elytrigia elongata=Agropyron elongatum.2n=70)杂交选育出来的5个八倍体小偃麦的染色体组进行了研究。通过八倍体小偃麦与普通小麦杂交,八倍体小偃麦相互间杂交,观察了杂种F_1花粉母细胞减数分裂行为。根据观察结果,讨论了长穗偃麦草染色体组的构成,认为长穗偃麦草的染色体组为E_1E_2F_2F_2N较为合适。在此基础上,确定了5个八倍体小偃麦的染色体组:7430为ABDE_1,68为ABDF_1,693为ABDF_1,7631为ABDF_2,784为ABDN。另外,还讨论了八倍体小偃麦染色组的重组问题。     

长穗偃麦草优异基因的染色体定位及应用

长穗偃麦草比较公认的有2个种,即二倍体长穗偃麦草(Thinopyrum elongatum,2n=2X)和十倍体长穗偃麦草(Thinopyrum ponticum,2n=10X),是重要的小麦近缘种,具有抗病、抗寒、抗旱、耐盐碱等优良性状。因其基因组中蕴含许多对小麦品种改良极为有用的基因,且易与小麦杂交等优势,多年来长穗偃麦草一直作为小麦遗传改良的优良种质资源而备受关注。本文对长穗偃麦草的基因组研究及其在小麦的抗逆、抗病和提高光合能力、产量及高分子量谷蛋白(HMW-GS)含量等方面的应用做了综述,为其基因组中优异基因的进一步开发和利用提供了理论依据。     

一个小麦-中间偃麦草异代换系的形态学和细胞学鉴定

中间偃麦草含有丰富的优良基因,在小麦的遗传改良中具有重要利用价值。对从中间偃麦草与小麦品种烟农15杂种后代(BC2F4)中选育的小麦种质系山农0095进行形态学和细胞学鉴定,结果表明：山农0095株高78cm,穗长17．3cm,旗叶长36．3cm,旗叶宽3．03cm,茎杆粗壮,繁茂性好,既长又宽的旗叶、长圆锥型穗是其显著的形态学特征;其根尖细胞染色体数日为2n=42,花粉母细胞减数分裂中期Ⅰ(PMC M Ⅰ)染色体构型为2n=21Ⅱ;它与普通小麦的杂种FⅠPMC M Ⅰ绝大多数细胞出现2个单价体,没有观察到多价体,平均染色体构型为2n=20．08Ⅱ 1．84Ⅰ。以上结果表明,山农0095是一个小麦-中间偃麦草的双体异代换系。     

一个异源胞质单体附加系小麦的遗传分析

以长穗偃麦草(Elytrigia elongata=Agropyron elongatum,2n=70)为母本,普通小麦为父本,进行核代换回交,在第九次回交的F_1(BC,F_1)代里,发现了一个异源胞质单体附加系小麦,代号E617。以E617做母本,普通小麦做父本进行杂交,杂种F_1出现正常株和弱株两种类型。正常株具有43条染色体,弱株具有42条染色体。反交,以普通小麦做母本,E617做父本,杂种F_1,无论是具有43条染色体还是具有42条染色体的植株,都是正常的。正反杂交结果表明,长穗偃麦草细胞质对普通小麦的细胞核产生了抑制作用,使核质杂种生长不正常,而附加一条特异的长穗偃麦草染色体(或端体),就能消除长穗偃麦草细胞质的抑制作用,使核质杂种恢复正常生长。     

抗黄矮病普通小麦偃麦草异附加系、异代换系的选育和鉴定

以偃麦草 (Ag .pulcherrimum)为抗源 ,以圆锥小麦 (T .turgidum)×偃麦草的双二倍体———CPI113 5 0 0 ( 2n =70 )与普通小麦杂交、回交、自交得到的衍生系为基础材料 ,利用黄矮病抗性追踪、形态学标记、细胞遗传学分析 ,筛选到 2个抗黄矮病新种质 96S16 11,96W 14 9.通过测交分析、原位杂交和同工酶电泳分析等技术 ,对以上材料进行鉴定 ,结果表明 :96S16 11为普通小麦 偃麦草二体异附加系 ,96W 14 9为普通小麦 偃麦草 1D( 1Ap)二体异代换系 .     

应用基因组原位杂交鉴定蓝粒小麦及其诱变后代

应用基因组原位杂交技术（GISH）对普通小麦（Triticum aestivumL.)和长穗偃麦草[Agropyron elongatum(Host)Beauv,2n=10x=70]杂交后选育出的蓝粒小麦蓝-58及其诱变后代的染色体组成进行了鉴定。结果表明,GISH可方便地检测到小麦遗传背景中的长穗偃麦草染色体或易位的片段。如前人报道,蓝-58（2n=42)是一个具有2条长穗偃麦草4E染色体的异代换系（4E/4D）。LW004可能是一个具有两对相互易位染色体的纯合系,其田间表现磷高效特性,LW43-3-4为41条染色体的蓝单体（40W 1’4E）,种子颜色为浅蓝色,通过此法还检测出一些染色体结构发生很大变异的材料如4E的单端体（40W 1‘4E),种子颜色为浅蓝色,通过此法还检测出一些染色结构发生很大变异的材料如4E的单端体（40W 1‘t4E)以及组型为39W 1‘4E 1‘t4E的个体,此项研究结果更为直观地表明控制蓝粒体状的基因的确在来自长穗偃麦草的染色体上。同时说明有效的突变方法与灵活方便的检测手段的有机结合在染色体工程材料的创制和染色体工程育种中起着至关重要的作用。     

抗条锈病小偃麦双体异附加系山农87074-519的鉴定

综合利用抗性接种鉴定、细胞学分析、SSR分子标记和基因组原位杂交(GISH)技术相结合的方法,对从长穗偃麦草与小麦复合杂交后代中选育的抗条锈病种质系山农87074-519进行了鉴定。结果表明,山农87074-519的根尖细胞染色体数目2n=44,花粉母细胞减数分裂中期I(PMCMI)绝大多数细胞内可观察到22个二价体,平均染色体构型2n=44=21.82Ⅱ 0.36Ⅰ,它与普通小麦中国春杂种F1的多数花粉母细胞内染色体构型为2n=21Ⅱ 1Ⅰ,因此它是1个附加了1对长穗偃麦草染色体的双体异附加系;以假鹅冠草St基因组总DNA作探针进行原位杂交发现山农87074-519的44条染色体中有2条出现黄绿色杂交信号,且杂交信号遍布整条染色体,证明其附加的长穗偃麦草染色体为St基组;利用SSR分子标记技术,在170对SSR引物中筛选出特异引物BARC165,它能稳定地在山农87074-519中扩增出长穗偃麦草特异标记BARC165268;将长穗偃麦草中BARC165的特异扩增片段克隆测序后制备成探针进行原位杂交,可在山农87074-519的间期染色体和有丝分裂中期染色体检测到杂交信号。山农87074-519综合农艺性状较好,对条锈病免疫,其抗性基因为显性,且位于附加的长穗偃麦草St基组染色体上,暂将其表示为YrSt。该种质系在小麦的遗传改良中具有重要利用价值。     

小麦与彭梯卡偃麦草杂种及其衍生后代的细胞遗传学研究──Ⅱ．来自小麦和彭梯卡（长穗）偃麦草及中间偃麦草杂种后代11个八倍体小偃麦的比较研究

利用染色体配对分析和酯酶及种子醇溶蛋白电泳分析研究了我国育成的１１个八倍体小偃麦,结果表明：（ａ）来源于小麦和中间偃麦草杂交后代的６个部分双二倍体中,中１和中２的偃麦草染色体组不同于中３、中４、中５和小偃７８８２９的偃麦草染色体组;（ｂ）来源于小麦和长穗偃麦草杂交后代的５个部分双二倍体中,小偃７８４的偃麦草染色体组不同于小偃６９３和小偃７６３１中的偃麦草染色体组,表明在长穗偃麦草中有两个互不相同又不同于小麦的染色体组Ｅ和Ｆ,而小偃７４３０和小偃６８中的偃麦草染色体组很可能是Ｅ和Ｆ染色体组的重组体;（ｃ）小偃７８４中的长穗偃麦草染色体组和中５及小偃７８８２９中的中间偃麦草染色体组基本相同,而中２的中间偃麦草染色体组不同于小偃６９３和小偃７６３１中的长穗偃麦草染色体组Ｆ,这意味着在长穗偃麦草和中间偃麦草中可能只有一个共同的染色体组Ｅ。部分双二倍体中酯酶及醇溶蛋白偃麦草染色体特征带的存在和发现,为这些染色体或其片段导入小麦后的鉴定提供了方便。     

“缺体回交法”选育普通小麦异代换系方法的研究

利用从蓝单体自交分离得到的自花结实的4D缺体小麦(缺72180、缺天选15)作母本与3个不同的八倍体小偃麦(小偃784、小偃7631和小偃78829)杂交,再以缺体作为轮回亲本,从F_1或F_2开始连续回交1—2次,在回交中,缺体无论作父本或母本都得到了异代换系,并且发现:(1)在回交过程中,用缺体作母本比作父本更为有效;(2)F_1自交,在F_2群体中选择生长比较正常,染色体数比较少的植株回交,比F_1作母本直接回交效果更好。并对所得的异代换系的特征特性进行了初步的观察研究,发现中间偃麦草(Agropyron intermedium2n=42) 4E染色体(以下用4Ei表示)、长穗偃麦草(Agropyron clongatum 2n=70)的4E染色体(带蓝粒基因,以下用4Ee表示)和4F染色体(带毛叶基因,以下用4Fe表示)均能正常补偿小麦4D染色体。异代换系生长旺盛,育性正常。初步总结了缺体与八倍体小偃麦杂交,回交过程中异代换系的形成规律,证明了“缺体回交法”可以推广应用于八倍体小偃麦等人工合成的新物种,以选育普通小麦异代换系。     

Photosynthetic capacity and dry mass partitioning in dwarf and semi-dwarf wheat (Triticum aestivum L.).

Efficient use of space and high yields are critical for long-term food production aboard the International Space Station. The selection of a full dwarf wheat (less than 30 cm tall) with high photosynthetic and yield potential is a necessary prerequisite for growing wheat in the controlled, volume-limited environments available aboard long-term spaceflight missions. This study evaluated the photosynthetic capacity and carbon partitioning of a full-dwarf wheat cultivar, Super Dwarf, which is routinely used in spaceflight studies aboard U.S. space shuttle and NASA/Mir missions and made comparisons with other dwarf and semi-dwarf wheat cultivars utilized in other ground-based studies in plant space biology. Photosynthetic capacity of the flag leaf in two dwarf (Super Dwarf, BB-19), and three semi-dwarf (Veery-10, Yecora Rojo, IBWSN 199) wheat cultivars (Triticum aestivum L.) was assessed by measuring: net maximum photosynthetic rate, RuBP carboxylation efficiency, chlorophyll concentration and flag leaf area. Dry mass partitioning of carbohydrates to the leaves, sheaths, stems and ear was also assessed. Plants were grown under controlled environmental conditions in three replicate studies: slightly enriched CO2 (370 micromoles mol-1), high photosynthetic photon flux (1000 micromoles m-2 s-1; 58 mol m-2 d-1) for a 16 h photoperiod, 22/15 degrees C day/night temperatures, ample nutrients and water provided by one-half strength Hoagland's nutrient solution (Hoagland and Arnon, 1950). Photosynthetic capacity of the flag leaf was determined at anthesis using net CO2 exchange rate versus internal CO2 concentration curves measured under saturating light (2000 micromoles m-2 s-1) and CO2 (1000 micromoles mol-1). Dwarf wheat cultivars had greater photosynthetic capacities than the taller semi-dwarfs, they averaged 20% higher maximum net photosynthetic rates compared to the taller semi-dwarfs, but these higher rates occurred only at anthesis, had slightly greater carboxylation efficiencies and significantly increased chlorophyll concentrations per unit leaf area. The reduced-height wheat had significantly less dry mass fraction in the stem but greater dry mass partitioned to the ear than the taller semi-dwarfs (Yecora rojo, IBWSN-199). Studies with detached heads confirm that the head is a significant sink in the shorter wheat cultivars.     

Dwarfing genes in the genus Lens Mill.

 Dwarfing genes were detected following intra- and interspecific hybridization in Lens. Dwarf phenotypes are controlled by two complementary dominant genes, Df ₁ and Df ₂. These two genes are suppressed by the dominant allele of the dwarf inhibitor genes, Dfi. The dominant allele of the Df gene was detected in L. ervoides from Ethiopia and Uganda and in a cultivated line of L. culinaris from Ethiopia, that of the Df ₂ gene in a L. ervoides accession from Israel. The dominant allele of the Dfi gene was detected in segregating populations of hybrids between L. ervoides accessions from Israel and Uganda. Using the homozygous dwarf, dfidfi, Df ₁ Df ₁, Df ₂ Df ₂ as the parent in interspecific crosses, we detected the dominant allele of the Dfi gene in one accession of L. nigricans and another of L. lamottei. The appearance of dwarf plants in segregating populations of hybrids between the cultivated line from Ethiopia and L. ervoides from Israel indicate that the cultivated line possesses the dominant allele of the Dfi gene. Dwarf plants were characterized by short internodes, a short leaf axis and smaller, convex leaflets. Spraying the dwarf plants with gibberellic acid induced internode and lead-axis elongation but had no effect on leaflet shape and size. When the dwarfs and their parental lines were grown in the dark they had the same internode length. Received: 12 April 1997 / Accepted: 25 June 1997     

矮败蓝标型小麦不育系的选育与研究

利用蓝粒太谷核不育硬粒小麦89-2343[AABB 4D(MS2)/4E]与普通小麦7739-3(2n=42)杂交、回交所产生的蓝粒可育株与白粒矮败材料杂交、回交,育成了一份矮败蓝粒小麦.选用13份遗传背景不同的白粒普通小麦与之杂交、回交,育成了13份矮败蓝粒小麦.对后代的粒色和育性分离进行分析,蓝粒矮败不育株占22.1%,白粒非矮秆可育株占77.7%,表明蓝粒基因、Ms2和Rht10均位于附加染色体上,且连锁紧密;但不同轮回亲本,矮败蓝粒的传递率有差异,477A的传递率最高,接近50%.细胞学分析表明矮败蓝粒小麦仍为单体附加系;探讨了矮败蓝粒小麦在群体改良和杂种小麦生产中的应用.     

一个新矮生玉米种质资源的发现与遗传鉴定

玉米矮生种质资源在育种工作中具有重要的利用价值。2002年在玉米种质资源扩繁与鉴定过程中,从玉米自交系K36中发现一株矮生突变体。随后通过连续自交,获得了纯合一致、稳定的矮生自交系,命名为矮2003。该矮秆材料在北京表现株高62．1cm,植株清秀,茎秆坚硬,结实正常。于不同时期用不同浓度赤霉素处理该材料显示其对赤霉素反应不敏感。矮2003与正常玉米自交系测交F1呈现高秆,F2与BC1高、矮秆分离比例分别符合3：1与1：1,遗传分析表明其矮生性状受一对主效单基因控制,表现为隐性遗传。所携带的矮生基因不同于已报道的玉米Dwarf8等。     

Molecular cytogenetic identification of a novel dwarf wheat line with introgressed <Emphasis Type="Italic">Thinopyrum ponticum</Emphasis> chromatin

Novel dwarfing germplasms and dwarfing genes are valuable for the wheat breeding. A novel semi-dwarf line, 31505-1, with reduced height compared with its common wheat parent, was derived from a cross between common wheat and Thinopyrum ponticum. Cytological studies demonstrated that 31505-1 contained 42 chromosomes and formed 21 bivalents at meiotic metaphase I. Genomic in situ hybridization (GISH) analysis showed that 31505-1 had no large Th. ponticum chromosome fragments. Fluorescence in situ hybridization (FISH) results revealed the absence of a pAs1 hybridization band on 2DL chromosome of 31505-1. Two SSR markers (Xwmc41 and Xcfd168) and two STS markers (Xmag4059 and Xmag3596), which were located on 2D chromosome, amplified unique bands of Th. Ponticum in 31505-1. These revealed presence of an introgressed Th. ponticum segment in 2DL chromosome of dwarf line 31505-1, although the alien segment could not be detected by GISH.     

施氮水平对小麦籽粒发育过程中氨基酸含量的影响

施氮能提高小麦籽粒蛋白质氨基酸的含量,并与施氮水平呈正相关;但对普通小麦必需氨基酸与蛋白质氨基酸的比值没有影响,而硬粒小麦4286随施氮水平的提高,该比值下降。在开花后32d以前,籽粒发育过程中游离氨基酸与施氮水平呈正相关,以后,籽粒中游离氨基酸趋于相近,表明施氮增加了游离氨基酸的库源,不同基因型小麦对施氮水平的反应不同,在同等施氮水平和栽培条件下,籽粒中蛋白质氨基酸和游离氨基酸含量为硬粒小麦4286＞小偃6号＞小偃107,不同施氮水平下,籽粒中氨基酸含量为高氮＞中氮＞低氮。     

Phenotypic Analysis of a Dwarf Wheat (Triticum aestivum L.) with Altered Phytochrome-Mediated Growth Responses

The influence of the amount of red light relative to far red light (red/far red ratio) on leaf-sheath elongation, leaf length, tillering, assimilate partitioning to shoots and roots, and chlorophyll content in a dwarf wheat (Triticum aestivum L. cv Tibet Dwarf) and seven other dwarf and standard cultivars was determined. All cultivars tested showed far red-stimulated leaf and leaf-sheath elongation except Tibet Dwarf. Tibet Dwarf was also unresponsive to a brief end-of-day exposure to far red light, although the other cultivars exhibited increased leaf-sheath and leaf length. In these cultivars, the effects of an end-of-day 5-min far red exposure were reversible by a subsequent 5-min red light exposure. Shoot/root ratios were higher and tillering was suppressed by increased far red irradiance in all cultivars except Tibet Dwarf. In addition, Tibet Dwarf was less responsive to dark-induced leaf and leaf-sheath elongation (etiolation) and retained chlorophyll in dark-adapted leaves longer than control cultivars. Tibet Dwarf did not differ from the other cultivars in leaf chlorophyll content. Western blot analysis, using an antibody against phytochrome A, showed that dark-grown Tibet Dwarf shoots contained at least twice the amount of detectable phytochrome A protein present in the other wheat cultivars. These results, plus the short, thick-stemmed, dark-pigmented phenotype of Tibet Dwarf suggest the possibility of a mutation in the phytochrome/signal transduction pathway.     

易组"太谷核不育基因"(Ms2)基因定位的研究

将在远缘杂交中由普通小麦（AABBDD）4D染色体易组导入六倍体小黑麦（AABBRR）以及硬粒小麦（AABB）的太谷核不育基因Ms2（原位于普通小麦4D染色体短臂距着丝点31．2cM的显性雄性不育核基因）。重新异回普通小麦染色体组中,所获得携带易组Ms2基因的新型太谷核不育小麦其显性雄性不育特性表达正常,且雄性不育株的雌性可育机制正常,对不育株幼穗花粉母细胞减数分型期染色体构型的观察可见其为整倍体（2n=42),尚未发现回归普通小麦的易组太谷核不育与原位 的太谷核不育基因有不同的表型。采用系统的标志基因测交法对回归普通小麦的易组太谷不育基因进行测交定位,发现易组Ms2基因与普通小麦显性秆标志基因Rht3连锁,从而将其定位于普通小麦4B 色体虎Rht3基因9.7cM处,新位点被命名为Ms2（4BS）,对Ms2基因在六倍体小黑麦与原太谷核不育小麦远缘杂交中位时的走向,普通小麦4A与4B染色体的互换更名以及Ms2（4BS）新位点的开发利用进行了讨论,认为异源多倍体生物核基因的组间易位倾向于从供体染色体向进化亲缘关系较密切,且染色体序数与染色体臂相同的部分同源染色体易位;1988年第7届国际小麦遗传学会对普通小麦4A与4B染色体的互换更名是正确的;Ms2（4BS）作为一个新型的遗传标记,作为小麦族内所有携带B染色体组的物种的育种工具和在拓建各为小麦种质资源的基因库等方面均有广泛的用途。     

Characterization of a dwarf gene in<Emphasis Type="Italic"> Brassica rapa</Emphasis>, including the identification of a candidate gene

Dwarf genes have been valuable for improving harvestable yield of several crop plants and may be useful in oilseed Brassica. We evaluated a dwarf gene, dwf2, from Brassica rapa in order to determine its phenotypic effects and genetic characteristics. The dwf2 mutant was insensitive to exogenous GA₃ for both plant height and flowering time, suggesting that it is not a mutation in the gibberellin biosynthesis pathway. The dwarf phenotype was controlled by a semidominant allele at a single locus. Near-isogenic lines that were homozygous or heterozygous for dwf2 had 47.4% or 30.0% reduction in plant height, respectively, compared to the tall wild-type line, and the reduction was due to reduced internode length and number of nodes. The dwf2 homozygous and heterozygous lines had the same or significantly higher numbers of primary branches than the wild-type line, but did not differ in flowering time. The DWF2 gene was mapped to the bottom of linkage group R6, in a region having homology to the top of Arabidopsis thaliana chromosome 2. The map position of DWF2 in comparison to markers in A. thaliana suggests it is a homolog of RGA (repressor of ga1-3), which is a homolog of the wheat Green Revolution gene. This dwarf gene could be used to gain more insight on the gibberellin pathway and to reduce lodging problems in hybrid oilseed Brassica cultivars.Communicated by J.S. Heslop-Harrison     

中国大麦矮秆种质资源的基因分析：Ⅰ.矮秆遗传和等位测验

了２４份中国大麦矮秆种质资源的株高遗传,在它们的矮秆基因之间且与已矮秆基因ｕｚ、ｓｄｗ、ｂｒ和ｅｎｓｏ进行遗传等位性测验。结果表明,这些矮秆种在多隐性单基因遗传,少数受隐性基因控制,只有１份携带１对隐性和１对不完全显性筹秆基因。