981 resultados para Classical nuclear import pathway


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核核糖体DNA(nrDNA)已被作为一个重要的标记,用于推断很多分类等级上的系统发育关系。相对于在被子植物中的快速致同进化,nrDNA在裸子植物中的致同进化速率低,且ITS和5S-NTS区有着较大的长度变异,这种现象在松科植物中尤为明显。在本研究中,我们克隆并测定了银杉属的5S rDNA以及冷杉属、银杉属、雪松属、油杉属、长苞铁杉属、金钱松属与铁杉属的ITS序列。基于获得的新数据,再结合前人报导的其它属的数据,我们探讨了如下四个问题: (1)松科 nrDNA ITS1 亚重复单位的组成、分布及进化;(2)ITS1区的长度变异与亚重复单位数目的关系以及它们的系统学意义;(3)松科ITS1的二级结构特征;(4)银杉5S rDNA编码区及非转录间隔区的结构特征。主要研究结果如下: 1. ITS区的序列分析ITS区的克隆及序列分析发现:(1) 松科ITS1的长度变异范围为 944-3271 bp, 这是目前已报导的真核生物中属间ITS变异最大的类群之一;(2) 所有松科植物的ITS区域都包含亚重复单位,亚重复单位的数目从2到9,并且这些亚重复单位可分为两种类型,即不含保守核心序列(5’-GGCCACCCTAGTC ) 的长亚重复单位(LSR)和含上述保守核心序列的短亚重复单位(SSR);(3) ITS1区的巨大长度变异主要归因于亚重复单位的数量变异; (4) ITS1区的GC含量与 它的序列长度和亚重复单位的数目有一定关系,并能够提供一些系统发育信息,特别是支持云杉属、松属和银杉属三者具有很近的亲缘关系。 2. ITS1亚重复单位的系统发育分析为了研究亚重复单位的进化关系,我们用最大似然法和最大简约法构建了松科ITS1亚重复单位的系统发育树。结果表明:(1)在ML和MP树中可发现有共同的五个分支; (2) 银杉比松科其它属拥有更多的SSR,且该属的所有9个SSR在系统树中构成一个单系支,表明它们是在银杉属内发生重复的;(3)一些SSR在属间和种间具有同源性,可为nrDNA ITS 的进化历史以及松科的系统发育 研究提供重要信息;(4)亚重复单位的多次重复以及伴随的重组可能是导致LSR 和SSR在松科不同属中分布式样不同的原因。 3. 松科ITS1的二级结构 用 Mfold 3.2 软件对松科所有11个属的ITS1区进行了二级结构预测,共获得了563个最低自由能折叠。结合以前关于松科二级结构的报导,我们分析的结果表明:(1) 松科ITS1的二级结构主要由几个延展的发夹结构组成;(2) 构象的复杂性与亚重复的数目呈正相关;(3)配对的亚重复单位通常在保守核心区(5’-GGCCACCCTAGTC ) 处有部分重叠,并且构成一个长茎,而其它的亚重复单位通常会自身折叠,且保守核心区的部分出现在发夹结构的环中。 4. 银杉5S rDNA 序列分析 我们对来自银杉不同群体的3个个体的5S rDNA进行了克隆,共获得 45 条序列,分析结果表明:(1) 绝大多数银杉5S rDNA编码区长度为120 bp, 以GGG 开头,以CTC结尾,编码区出现的碱基替代主要为转换;(2) 银杉与其它裸子植物相比,5S rDNA基因编码区具很高的相似性(90-99%); (3)间隔区含有一个poly-C和一个poly-T结构、两个TC丰富区以及五个GC丰富区。根据长度和序列特征,银杉的5S rDNA间隔区可分为三种类型:Type A 长751-764 bp,Type B 长770-807 bp (含一个32 bp的插入),Type C 长581-594 bp; (5)长间隔区(Type A,Type B )中含有两个148-175 bp的串联亚重复单位,该亚重复单位与短间隔区(Type C )中的一段143 bp的序列具有较高的相似性(56.0-66.8%)。 5. 银杉5S rRNA的二级结构 Mfold 3.2 预测结果表明:(1)银杉5S rRNA二级结构包括5个双螺旋区(干区)(Ⅰ-Ⅴ)、2个发夹结构环区(C和D)、3个中间环区(B1、B2 和 E)和1个铰链区(A), 铰链区为三个双螺旋的结合处;(2) 二级结构中的环区通常比双螺旋区更加保守;(3)在5个双螺旋中,I 和 IV 区有较高的碱基替代率。

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Nuclear RNA and DNA in muscle cell nuclei of laboratory-reared larvae of Walleye Pollock (Gadus chalcogrammus) were simultaneously measured through the use of flow cytometry for cell-cycle analysis during 2009–11. The addition of nuclear RNA as a covariate increased by 4% the classification accuracy of a discriminant analysis model that used cell-cycle, temperature, and standard length to measure larval condition, compared with a model without it. The greatest improvement, a 7% increase in accuracy, was observed for small larvae (<6.00 mm). Nuclear RNA content varied with rearing temperature, increasing as temperature decreased. There was a loss of DNA when larvae were frozen and thawed because the percentage of cells in the DNA synthesis cell-cycle phase decreased, but DNA content was stable during storage of frozen tissue.

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For more than 25 years all sea turtle products have been prohibited from international commerce by the 170-member nations of the Convention on International Trade in Endangered Species (CITES). Sea turtles continue to be threatened by direct take (including poaching) and illegal trade despite multi-national protection efforts. Although take may contribute significantly to sea turtle decline, illegal take is difficult to measure since there are few quantified records associated with legal fisheries and fewer still for illegal take (poaching). We can, however, quantify one portion of the illegal sea turtle trade by determining how many illegal products were seized at United States ports of entry over a recent 10-year period. The United States Fish and Wildlife Service (USFWS) oversees the import and export of wildlife and wildlife products, ensuring that wildlife trade complies with United States laws and international treaties. Additionally, the USFWS has legal authority to target suspected illegal wildlife activity through undercover and field investigations. In an effort to assess the scale of illegal sea turtle take and trade, we have conducted a 10-year (1994 – 2003) review of the law enforcement database maintained by the USFWS. This database tracks the number and type of wildlife cases, the quantity of seized products, and the penalties assessed against violators. These data are minimum estimates of the sea turtle products passing through the United States borders, as smuggled wildlife is oftentimes not detected.

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Independent molecular markers based on mitochondrial and nuclear DNA were developed to provide positive identification of istiophorid and xiphiid billfishes (marlins, spearfishes, sailfish, and swordfish). Both classes of markers were based on amplification of short segments (<1.7 kb) of DNA by the polymerase chain reaction and subsequent digestion with informative restriction endonucleases. Candidate markers were evaluated for their ability to discriminate among the different species and the level of intraspecific variation they exhibited. The selected markers require no more than two restriction digestions to allow unambiguous identification, although it was not possible to distinguish between white marlin and striped marlin with any of the genetic characters screened in our study. Individuals collected from throughout each species’ range were surveyed with the selected markers demonstrating low levels of intraspecific character variation within species. The resulting keys provide two independent means for the forensic identification of fillets and for specific identification of early life history stages.

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Recent developments in aquaculture has created an awareness that prawn culture is a dollar spinner, in which industry can step in to earn foreign exchange by producing an expensive food iten which has a high market demand abroad. The Government has to take a policy decision whether the prawn culture should be done through small fishermen to improve their socio-economic condition or through private industry with the high technology input and predefined objectives of export trade. Perhaps a simultaneous operation of the two could be allowed best in the interest of India. Perhaps in the interest of quick development and adoption of high production technology, through fishermen organization, the development is encouraged through the implimentation of welfare and area development schemes. In some selected areas private industry may be encoureged to use high production technology to develop prawns.