无叶莲科,缅甸被子植物一新记录科（英文）

近期在缅甸北部进行野外植物考察中,发现了一种菌类寄生植物,疏花无叶莲(Petrosaviasakurai),是缅甸被子植物一新记录科和新记录目——无叶莲科和无叶莲目。对其进行了详细的报导,并提供特征描述等数据。疏花无叶莲主要特征为茎上的鳞片状叶较疏离且彼此相距1～2 cm、总状花序、花苞片稍短于花梗、花被约1/3贴生于子房上。     

江西省种子植物一新记录科(无叶莲科)及其生物地理学意义

报道江西省种子植物一新记录无叶莲科Petrosaviaceae无叶莲属Petrosavia Beccari疏花无叶莲Petrosavia sakurai(Makino)J.J.Smith ex van Steenis。无叶莲科为江西省新记录科。该种是晚第三纪古热带森林植被的残余种,此次发现于江西井冈山地区笔架山海拔约1200 m的山地常绿阔叶林中,对进一步揭示该地区残存的季雨林植被特征具有重要意义。     

通过构建三段T-DNA载体高频率获得无标记转基因大豆植株的研究

高频率获得无选择标记转基因植株有利于转基因植物的环境释放和安全性生产,农杆菌介导的共转化法是获得无标记转基因植株的方法之一。含二段T-DNA载体的共转化法已被人们成功应用,而二段以上T-DNA载体的共转化法还未见报道。基于这一目的,通过几个中间质粒构建了含有三段T-DNA的双元表达载体pNB35SVIP1,其中包含1个拷贝bar基因选择标记基因表达盒和2个拷贝VIP1目的基因表达盒。利用EHA101农杆菌菌系介导法转化大豆子叶节,经过在含3～5mg/L glufosinate培养基上多次筛选,获得了一定数量抗性再生植株,然后对抗性再生植株进行叶片涂抹除草剂、Southern blot和Northern blot检测,共鉴定出51棵T₀代转基因植株,转化频率0.83%～3.16%,二个基因的共转化频率为86.4%。在对T₁代群体进行叶片涂抹除草剂检测的基础上,不抗除草剂植株进行PCR、Southern blot和Northern blot检测,共鉴定出41棵无选择标记转基因植株,无标记植株获得率为7.6%。检测结果还表明,T₁代群体中22.7%的株系发生了基因丢失现象,27.3%的株系发生了bar基因沉默现象,目的基因在37.1%的无标记植株中发生了沉默现象。三段T-DNA的双元表达载体是获得无标记转基因植株的理想途径     

中国17种蔷薇属植物45S和5S的rDNA分布研究

为了探寻蔷薇属植物亲缘关系及系统发育研究的分子细胞遗传学证据,该研究采用双色FISH(荧光原位杂交)技术,对原产中国7个组的17种蔷薇属植物的45S和5S rDNA进行了定位分析。结果表明:(1)多数蔷薇属植物1组染色体对应1个45S rDNA位点和1个或2个5S rDNA位点,偶尔出现1~2个rDNA位点的丢失,但复伞房蔷薇(Rosa brunonii)的1组染色体对应了2个45S rDNA位点。(2)二倍体的蔷薇属植物至少有1对5S rDNA位点与45S rDNA位点共定位,而四倍体材料的5S rDNA位点与45S rDNA位点没有共定位,但所有四倍体材料均至少有1种rDNA信号纯合,表明它们应为二倍体直接加倍产生的同源四倍体。(3)绝大多数材料45S rDNA位于染色体短臂、5S rDNA位于染色体长臂,但缫丝花(R. roxburghii f. roxburghii)有1个5S rDNA信号位于染色体的短臂上,表明它与蔷薇属其他种的亲缘关系较远。(4)阿克苏地区和伊犁地区的疏花蔷薇的核型不同,且45S和5S rDNA的数量和位置不同,分子细胞遗传学证据也支持阿克苏地区的疏花蔷薇应为疏花蔷薇的新变种。(5)该研究中共有8个二倍体和6个四倍体蔷薇属植物的双色FISH为首次报道。研究认为,无论二倍体还是四倍体蔷薇属植物中出现的异形同源染色体、rDNA信号位置在同源染色体上的差异以及rDNA信号的增加和丢失,可能都与染色体结构变异和染色体重组有关,在分子细胞遗传学水平上证明染色体结构变异和染色体重组在蔷薇属植物演化过程中具有重要的作用。     

广西中部下泥盆统无颌类和鱼类微体化石——兼论桂中与滇东下泥盆统的对比*

记述了广西横县六景那高岭组、郁江组,武宣二塘二塘组和象州大乐四排组(大乐组)的无颌类和鱼类微体化石。经过形态学和古组织学的研究,这些化石被归于13属(其中包括1新属、2未定属)11种(其中包括3新种4未定种和1比较种)。结合以往在莲花山组和那高岭组下部已报道的脊椎动物大化石资料讨论了广西中部下泥盆统的脊椎动物组合序列:莲花山组以Yunnanolepis-Qujinolepis组合,那高岭组以Asiaspis expansa-Machaeracanthus? bohemicus组合,郁江组以Turinia sp.-Cheiracanthoides comptus-Ohiolepis newberryi组合,二塘组以Nostolepis guangxinensis-Wuxuanichthys wangi-Ligulalepis cf. toombsi组合为代表。另外,据已报道的脊椎动物微体化石和大化石资料,对广西中部和云南东部下泥盆统进行了对比。     

金黄色葡萄球菌tst-1基因敲除菌株的构建

抽提金黄色葡萄球菌834菌株的基因组DNA,PCR克隆扩增tst-1及tst-1的上、下游基因,通过将tst-1上、下游基因分别重组到载体质粒pAULA中,形成同源重组质粒pAULA Δtst-1,将pAULA-Δtst-1电转入细菌内,进行同源重组,以PCR、Western blot鉴定tst-1基因敲除菌株无tst-1基因片段,且无TSST-1蛋白表达,表明已成功构建金黄色葡萄球菌tst-1基因的敲除菌株。     

中国哥纳香属(番荔枝科)植物新资料

番荔枝科(Annonaceae)是基部被子植物木兰目(Magnoliales)中较进化且物种数最多的科。目前的系统发育研究将番荔枝科划分为4个亚科,即蒙蒿子亚科(Anaxagoreoideae)、澄光木亚科(Ambavioideae)、番荔枝亚科(Annonoideae)和排石木亚科(Malmeoideae),有107属,2 400多种,中国原产21 属约110 种。番荔枝科泛热带分布,是热带植物区系的优势类群,中国云南盈江位于云南省最西部边境,与缅甸东北部接壤,并与印度的东阿萨姆较近,植物区系处于东南亚(印度—马来西亚)热带生物区系向东亚亚热带-温带生物区系的过渡地带,属典型热带北缘性质,在植被地理和生物地理上十分重要,成为生物多样性保护的关键和热点地区。该区的热带雨林是印度阿萨姆和缅甸北部的热带雨林向东和向北扩散分布的边缘类型,是东南亚热带雨林在纬度和海拔分布上的极限类型。该文报道了采自中国云南省盈江县,引种保存于中国科学院西双版纳热带植物园的番荔枝科哥纳香属2个中国新记录种,即皱叶哥纳香 [Goniothalamus sesquipedalis(Colebr. ex Wall.)Hook. f. & Thomson]和长梗哥纳香(G. peduncularis King & Prain)。Flora of China将盈江哥纳香(G. lii X. L. Hou & Y. M. Shui)处理为云南哥纳香(G. yunnanensis W. T. Wang)的异名,基于活植物观察、馆藏标本和文献研究,该文对盈江哥纳香的分类地位进行了澄清,将其处理为长梗哥纳香的异名。皱叶哥纳香原记载产于印度、孟加拉国和缅甸等地,长梗哥纳香仅产于缅甸,该文对它们进行了补充描述,并提供彩色图版以便于鉴别。凭证标本存放于中国科学院西双版纳热带植物园标本馆(HITBC)。哥纳香属2个新记录的发现,丰富了中国番荔枝科植物多样性的认识,为中国云南热带植物区系属于热带亚洲(印度—马来西亚)植物区系,以及与缅甸北部、印度东北部植物区系的关系增加了例证。     

钟冠报春苣苔(苦苣苔科)的分类鉴定

原唇柱苣苔属(Chirita Buch.-Ham. ex D. Don)为一个人为界定的属, 2011年在分子系统学研究的基础上对该属及其近缘属开展了系统发育重建工作,其中绝大部分的原唇柱苣苔属唇柱苣苔组(Sect. Gibbosaccus C. B. Clark)的物种被并入了广义报春苣苔属(Primulina Hance)。然而,由于历史原因和早期经典分类学在研究方法上的局限性以及对现报春苣苔属部分物种的营养器官与生殖器官的认知不够,该属下一些物种的分类仍存在一些问题,亟待深入研究。比如,在对中国和越南分布的苦苣苔科植物开展研究的过程中,作者发现两个报春苣苔属的物种——广布于中国西南和华南直至中南半岛中部的钟冠报春苣苔[Primulina swinglei(Merr.)Mich. Möller & A. Weber]命名人和原被认为是中国与广西特有种的疏花报春苣苔[P. laxiflora(W. T. Wang)Yin. Z. Wang]之间的鉴定存在分类学问题,需要进一步厘清两者之间的关系。该文对这两个物种进行了形态比较,同时通过对这两种植物的原始描述对比、植物标本检查、栽培观察以及野外实地观察,确定疏花报春苣苔是钟冠报春苣苔的异名。此外,还明确了钟冠报春苣苔的后选指定模式标本。     

缅甸紫金牛属新记录

报道了缅甸克钦邦分布的报春花科(Primulaceae)紫金牛属(Ardisia Swtarz)的3 新记录种:伞形紫金牛(Ardisia corymbifera Mez)、珍珠伞(Ardisia maculosa Mez)和Ardisia interjacens C. M. Hu & J. E. Vidal。     

青南、藏北中侏罗世缅甸贝内部构造的研究及修订*

通过缅甸贝内部构造及解剖学特征的研究和对比,对该属进行了修订和整理.发现过去置于该属中的90余种实际上包括了现在理解的9个以上属的内容.经与相近属内部和外部特征的比较,对缅甸贝的起源和演化做了初步研究.提出该属在晚 Bajocian 期起源于 Formosarhynchia,早 Bathonian 期得到了爆发性的发展和辐射,并在中、晚 Bathonian 期朝3个方向演化.通过对该属时空分布、共生生物、群落结构、伴生沉积岩及介壳稳定同位素和微量元素的综合分析,认为 Burmirhynchia-Holcothyris 群落主要生活于近岸浅水、含盐度偏低、水深可能小于 30m 的低能环境.     

The C. elegans sex determination gene laf-1 encodes a putative DEAD-box RNA helicase

The Caenorhabditis elegans gene laf-1 is critical for both embryonic development and sex determination. Laf-1 is thought to promote male cell fates by negatively regulating expression of tra-2 in both hermaphrodites and males. We cloned laf-1 and established that it encodes a putative DEAD-box RNA helicase related to Saccharomyces cerevisiae Ded1p and Drosophila Vasa. Three sequenced laf-1 mutations are missense alleles affecting a small region of the protein in or near helicase motif III. We demonstrate that the phenotypes resulting from laf-1 mutations are due to loss or reduction of laf-1 function, and that both laf-1 and a related helicase vbh-1 function in germline sex determination. Laf-1 mRNA is expressed in both males and hermaphrodites and in both the germline and soma of hermaphrodites. It is expressed at all developmental stages and is most abundant in embryos. LAF-1 is predominantly, if not exclusively, cytoplasmic and colocalizes with PGL-1 in P granules of germline precursor cells. Previous results suggest that laf-1 functions to negatively regulate expression of the sex determination protein TRA-2, and we find that the abundance of TRA-2 is modestly elevated in laf-1/+ females. We discuss potential functions of LAF-1 as a helicase and its roles in sex determination.     

Characterization of SLFL1, a pollen-expressed F-box gene located in the Prunus S locus

The S locus and its flanking regions in the genus Prunus (Rosaceae) contain four pollen-expressed F-box genes. These genes contain the S locus F-box genes with low allelic sequence polymorphism genes 1, 2, and 3 (SLFL1, SLFL2, and SLFL3) as well as the putative pollen S gene, named the S haplotype-specific F-box protein gene (SFB). As much less information is available on the function of SLFLs than that of SFB, we analyzed the SLFLs of six S haplotypes of sweet cherry (Prunus avium) in this study. Genomic DNA blot analysis and the isolation of SLFL1 showed that the SLFL1 gene in a functional self-incompatible S ³ haplotype is deleted and only a partial sequence resembling SLFL1 is left in the S ³ locus region, suggesting that SLFL1 by itself is not directly involved in either the GSI reaction or pollen-tube growth. Genomic DNA blot analysis showed that there was no substantial modification or mutation in SLFL2 and SLFL3. A phylogenic analysis of F-box genes in the rosaceous S locus and its border regions showed that Prunus SLFLs were more closely related to maloid S locus F-box brothers than to Prunus SFBs. The functions of SLFLs and the evolution of self-incompatibility in Prunus are discussed based on these results. Electronic supplementary material  The online version of this article (doi:) contains supplementary material, which is available to authorized users. The nucleotide sequence data reported appear in the DDBJ, EMBL, and GenBank Nucleotide Sequence Databases under the accession numbers, AB360339, AB360340, AB360341, and AB360342, for SLFL1-S ¹ , SLFL1-S ² , SLFL1-S ⁵ , and SLFL1-S ⁶ , respectively.     

TFS1: A suppressor of cdc25 mutations in Saccharomyces cerevisiae

Summary The TFS1 gene of Saccharomyces cerevisiae is a dosage-dependent suppressor of cdc25 mutations. Overexpression of TFS1 does not alleviate defects of temperature-sensitive adenylyl cyclase (cdc35) or ras2 disruption mutations. The ability of TFS1 to suppress cdc25 is allele specific: the temperature-sensitive cdc25-1 mutation is suppressed efficiently but the cdc25-5 mutation and two disruption mutations are only partially suppressed. TFS1 maps to a previously undefined locus on chromosome XII between RDN1 and CDC42. The DNA sequence of TFS1 contains a single long open reading frame encoding a 219 amino acid polypeptide that is similar in sequence to two mammalian brain proteins. Insertion and deletion mutations in TFS1 are haploviable, indicating that TFS1 is not essential for growth.     

Autonomy of the wingless mutation in Drosophila melanogaster

Summary T(Y;2) translocations were used to cytologically localise the wingless locus of Drosophila melanogaster. We found that an existing T(Y;2), which is an insertion of a segment of 2L into the Y chromosome, has wg ⁺ within this insert. This Y chromosome was used to generate an attached XY chromosome containing wg ⁺. The mutation claret-nondisjunctional (ca ^nd) was used to induce the loss of this XY chromosome and thus generate gynandromorphs with wg ¹/wg ¹ male tissue and wg ⁺/wg ¹/wg ¹ female tissue. Analysis of these gynanders demonstrated that a genotypically wingless mutant hemithorax is usually also phenotypically mutant in these half body mosaics; thus wg ¹ is discautonomous. This observation is of interest as it is known that wg is not cell autonomous.     

The <Emphasis Type="Italic">Caenorhabditis</Emphasis><Emphasis Type="Italic">briggsae</Emphasis> genome contains active <Emphasis Type="Italic">CbmaT1</Emphasis> and <Emphasis Type="Italic">Tcb1</Emphasis> transposons

The maT clade of transposons is a group of transposable elements intermediate in sequence and predicted protein structure to mariner and Tc transposons, with a distribution thus far limited to a few invertebrate species. We present evidence, based on searches of publicly available databases, that the nematode Caenorhabditis briggsae has several maT-like transposons, which we have designated as CbmaT elements, dispersed throughout its genome. We also describe two additional transposon sequences that probably share their evolutionary history with the CbmaT transposons. One resembles a fold back variant of a CbmaT element, with long (380-bp) inverted terminal repeats (ITRs) that show a high degree (71%) of identity to CbmaT1. The other, which shares only the 26-bp ITR sequences with one of the CbmaT variants, is present in eight nearly identical copies, but does not have a transposase gene and may therefore be cross mobilised by a CbmaT transposase. Using PCR-based mobility assays, we show that CbmaT1 transposons are capable of excising from the C. briggsae genome. CbmaT1 excised approximately 500 times less frequently than Tcb1 in the reference strain AF16, but both CbmaT1 and Tcb1 excised at extremely high frequencies in the HK105 strain. The HK105 strain also exhibited a high frequency of spontaneous induction of unc-22 mutants, suggesting that it may be a mutator strain of C. briggsae.     

Overexpression of <Emphasis Type="Italic">Arabidopsis</Emphasis> damaged DNA binding protein 1A (DDB1A) enhances UV tolerance

Damaged DNA Binding protein 1 (DDB1) is a conserved protein and a component of multiple cellular complexes. Arabidopsis has two homologues of DDB1: DDB1A and DDB1B. In this study we examine the role of DDB1A in Arabidopsis UV tolerance and DNA repair using a DDB1A null mutant (ddb1a) and overexpression lines. DDB1A overexpression lines showed higher levels of UV-resistance than wild-type in a range of assays as well as faster DNA repair. However a significant difference between wild-type plants and ddb1a mutants was only observed immediately following UV treatment in root length and photoproduct repair assays. DDB1A and DDB1B mRNA levels increased 3 h after UV exposure and DDB1A is required for UV regulation of DDB1B and DDB2 mRNA levels. In conclusion, while DDB1A is sufficient to increase Arabidopsis UV tolerance, it is only necessary for immediate response to UV damage.