<i>VvAGAMOUS</i> Affect Development of Four Different Grape Species Ovary

Grape pistil has an important influence on fruit size and quality. However, there were few studies on grape ovary, and the development process of the ovary is still unclear. Therefore, in this paper, four different grape varieties with different lengths of small inflorescences, namely ‘Musct Hambourg’ grape (Vitis vinifera), ‘Concord’ grape (Vitis labrusca), ‘ShanPuTao’ grape (Vitis amurensis) and ‘GongNiang2Hao’ grape (Vitis amurensis × Vitis vinifera) were used as test materials. Four varieties ovary were significant differences by means of stereomicroscope, paraffin section. The expression of ovary determining gene VvAGAMOUS (VvAG) and its development related genes VvCRABS CLAW (VvCRC) andVvAGAMOUS-LIKE 11 (VvAGL11) with similar functions during the development of different grape varieties were preliminarily explored using fluorescence quantitative test. The relationship between VvAG and VvCRC, VvAG and VvAGL11 were analyzed using Y1H assay. Our results showed that there were obvious abdominal sutures on the surface of expect for ‘Musct Hambourg’ grape, and existing poly carpels. The ovary development of ‘ShanPuTao’ and ‘GongNiang2Hao’ grape was completed when the inflorescence length was less than 1 cm, while the ‘Concord’ and ‘Musct Hambourg’ grape were fully developed when the length of inflorescence was 3–4 and 4–5 cm, respectively. VvAG and VvCRC began to express in large quantities after the formation of stamen primordia, while VvAGL11 during the forming of ovule primordia. Therefore, VvAG and VvCRC mainly regulated the development of stamens and carpels and also promote the development of ovules, while VvAGL11 major regulated the development of ovules. The promoters of VvCRC and VvAGL11 were bound by VvAG. This study provides an important theoretical basis for further research on the molecular mechanism of grape ovary development.     

鸭蛋黄颜色的生态遗传分析

1 引言 蛋黄颜色作为衡量禽蛋质量的主要经济性状之一,愈来愈受到消费者的关注,家鸡中这种性状的遗传力很低。Farnsworth等(1955)发现其遗传力为0.15,Torges报道其仅为0.05,Vanchev等(1980)估测母系遗传力为0.18,父系为0.47。因此,决定蛋黄色度主要是饲料因素,饲料中的氧化类胡萝卜素(叶黄素和玉米黄质)为蛋黄提供色素来源,能大量提供有效类胡萝卜素的饲料有藻类、紫花苜蓿、黄(白)玉米、大豆等植物,甲壳类动物、微生物(醇母)及类胡萝卜素制剂Mackey分别用墨角藻(Fucus vesiculosus)、齿缘墨角藻     

金银花花形基因的发掘及生物信息学分析

金银花作为我国重要的中药材,具有消炎、抗菌、抗病毒、抗氧化、防癌等多种功效。随着金银花市场供需矛盾日益加剧,通过分子标记辅助选择育种方法来培育高产优质品种势在必行。通过NCBI的Blast工具扫描金银花蛋白组数据发掘花形候选基因,并执行候选基因的亲缘关系分析、结构域分析、表达模式分析、理化性质分析、蛋白质结构预测等一系列生物信息学分析。依据拟南芥调控花形的ABE类基因,通过NCBI-Blast工具扫描金银花氨基酸序列,筛选出包含MADS结构域的8个调控花形的金银花候选基因。经LjaFGD表达模式分析发现,金银花的花中GWHGAAZE016592和GWHGAAZE014905表达量显著高于其他部位,可能正向调控金银花花形。GWHGAAZE014905是一个包含MADS结构域的调控花器官发育的B类基因;GWHGAAZE016592是AP3同源基因。生物信息学分析发现,GWHGAAZE016592和GWHGAAZE014905均是稳定的亲水蛋白,属于非分泌蛋白,包括Motif1、Motif3、Motif4、Motif2、Motif6和Motif5,蛋白质三级结构模板为6byy.2.A和4ox0.2.C。GWHGAAZE014905被定位到细胞核上,而GWHGAAZE016592被定位到叶绿体上,且包含1个位于151~173 bp的跨膜螺旋区域,属于膜蛋白。研究结果为分子标记辅助选择方式培育道地高产优质金银花品种提供了基因资源和分子标记。     

珍稀濒危植物细果秤锤树开花生物学特性和繁育系统

为了解珍稀濒危植物细果秤锤树（Sinojackia microcarpa）开花特征和有性繁殖,对其花部形态特征、开花动态、花粉胚珠比（P/O）、柱头可授性、花粉活力、套袋试验、访花昆虫及访花频率进行观测。结果表明：（1）细果秤锤树的杂交指数（OCI）为4,单花期5~7 d,种群花期可持续20 d左右。花粉与胚珠比为4 093.21±498.56。开花后第3天的花粉活力最高（76.21%）,而开花后第7天时花粉活力较低（18.37%）。细果秤锤树柱头最适可授期在开花后第2天。（2）套袋试验表明,细果秤锤树存在部分自交不亲和性,同时不存在无融合生殖,传粉昆虫是其完成生殖过程所必需的,且异株授粉能够提高其坐果率和结籽率。细果秤锤树的访花昆虫有3目5科7种,主要访花昆虫有黄胸木蜂（Xylocopa appendiculata）、熊蜂（Bombus sp.）、胡蜂（Vespa sp.）、中华蜜蜂（Apis cerana）、黑带食蚜蝇（Episyrphus balteatus）、其中熊蜂平均访花频率最高,达（8.67±0.21） 次·h^-1。对该物种开花生物学特征与繁育系统进行深入研究,有利于进一步探究其濒危机制,为后续珍稀濒危植物的研究提供理论依据和参考。     

Geographic variation for colour in the sandburrowing beetle Chaerodes trachyscelides White (Goleoptera: Tenebrionidae) on New Zealand beaches analysed using CIELAB L * values

Chaerodes trachyscelides White is a highly specialized, flightless burrowing beetle confined to the narrow strip of sand at and just above high water level on sandy marine beaches in New Zealand. Although the ventral surface of the beetle is always pale, the dorsal surface varies from pale to almost black. Large samples of this beetle were taken, together with the sand, from 11 beaches on New Zealand's three main islands. The colour of the dorsal surface of each individual beetle and that of the sand samples was measured using reflectance spectroscopy and expressed as CIE L*,a*,b* (CIELAB) values. The L* values, which are objective, quantitative measures of the degree of lightness of the beetles, were subjected to statistical and frequency analysis. Although the species was very variable in colour and the variation appeared to be continuous, a highly significant correlation was obtained between the mean of the L* values for the samples on each beach and that of the sand, the correlation coefficient being 0.961. This close association between the lightness of the beetles and that of the sand suggests the variable melanism functions as cryptic colouration. On most beaches, the distribution oflightness among the beetles sampled conformed to a normal curve. For beetles from sites where the sand was relatively uniform, such as the black Taranaki beaches, the L* frequency distribution curves were narrow and the coefficient of variation of mean beetle colour was relatively small indicating low colour variability. In contrast, the greatest within-site variability occurred on the two Stewart Island beaches sampled, where in each case there was less uniformity in the colour of the sand. At one of these sites, Maori Beach, darker sand present below the high water level is often deposited on the zone occupied by the beetles after storms. On Lonneker's Beach, the distribution of L* values among the beetles sampled was actually bimodal. On this small beach, there was an area of intensely black sand in the zone occupied by the beetles, but most of the rest was covered with light golden sand. These results are interpreted as evidence that the variability of colour of Chaerodes beetles has the effect of populations being able to match the colour of the sand of their home beaches, presumably as a consequence of the differential survival of individuals.     

Effects of temperature and photoperiod on flowering in Hyptis brevipes

Few tropical species have been tested for their flowering response under controlled conditions. Hyptis brevipes Poit, is an annual herb, commonly found in wet margins of streams and ponds, being considered a weed for some perennial plantations in Brazil. Under experimental glasshouse conditions, this species proved to be an obligate short-day plant. Flowering was delayed when photoperiods longer than 8 h were given, the critical photoperiod being between 12 and 13 h. When both temperature and photoperiod were controlled, at 20°C a longer protoperiod (by almost 1 h) is still inductive compared to 25 and 30°C. The number of short-day cycles required for full induction is relatively high and dependent upon temperature; at 20°C or above, 10 cycles are adequate, but at 15°C, more short-day cycles are needed. The number of inflorescences formed as well as the floral index vary according to daylength × temperature × inductive cycle number, allowing flowering to be assessed quantitatively. Long days are inhibitory to flowering, either suppressing it completely (when symmetrically intercalated among 24 inductive cycles) or preventing the floral index from increasing.     

Further studies on the effects of different auxins and cytokinins on flower formation in thin cell layers of Nicotiana tabacum: The effects of zeatin riboside, dihydrozeatin and dihydrozeatin riboside

Organogenesis in thin cell layers of Nicotiana tabacum L. was studied in relation to the effects of natural and synthetic auxins in combination with various cytokinins. All cytokinins tested, benzyladenine (BA), kinetin, zeatin (Z), zeatin riboside (ZR), N⁶-Δ²-isopentenyl) adenine (IPA), dihydrozeatin [(diH)Z] and dihydrozeatin riboside [(diH)ZR], seem to be active in flower bud formation. In addition to the initiation of flower buds, vegetative buds or roots were also formed on the explants in the presence of BA, Z or IPA as exogenous cytokinins. Only dihydrozeatin and its riboside stimulated the initation of flower buds alone (as is known for kinetin), especially if supplemented with indole-3-acetic acid (IAA) as exogenous auxin. A high number of explants with flower buds was also found with high cytokinin/2,4-D ratios. In these conditions the presence of (diH)Z yielded the higest number of flower buds per explant.     

The pale brown allele in Cepaea nemoralis

The pale brown colour morph in Cepaea nemoralis appears to be determined by an allele at the C (colour) locus ( C ^{P B}). Pale brown is dominant to yellow, codominant with pink and recessive to dark brown. It is linked to the B locus (which controls the presence or absence of banding on the shell), but not to the U locus, which determines whether there is one band or five. In segregations of pale brown and yellow there is a significant deficiency of pale brown, suggesting that there are differences in viability between the morphs.     

The causes of colour and colour change in caterpillars of the poplar and eyed hawkmoths (Laothoe populi and Smerinthus ocellata)

Caterpillars of the poplar and eyed hawkmoths (Laothoe populi and Smerinthus ocellata respectively) were reared under different conditions in order to determine why final instar caterpillars vary in colour. Poplar hawkmoth caterpillars normally rest on the undersides of leaves. Dull green and redspotted caterpillars are genetically determined polymorphisms. Caterpillars that are not dull green, however, can become white when fed on Populus alba or yellow-green when fed on Salix fragilis. Experiments showed that it is the reflective qualities of the leaves that determines which colour the caterpillar develops: if the young larva sees white then it becomes white, but if it sees green, grey or black then it becomes yellow-green. Young eyed hawkmoth larvae always developed into grey-green final instar caterpillars under our rather poorly-illuminated rearing conditions, but when reared on wild plants in white muslin sleeves they became whitish-green. In this species also it appears that colour of the final instar is determined by the reflectance of the substrate perceived by the young caterpillar.     

反义RNA技术在植物基因工程领域中的应用

反义RNA技术在植物基因工程领域中的应用包括：a．番茄和其他水果的成熟控制;b．植物的抗病性;c．改变花卉的颜色;d．植物淀粉合成的控制;e．油料植物种子中脂肪酸合成的控制;f．杂交种子生产中雄性不育性的控制;g．其他.