细胞色素b基因序列与7种石首鱼类的系统进化

通过比较一段381bp细胞色素b基因序列，分析了石首鱼科7种石首鱼的系统发育关系．该序列有51个单变异多态位点、128个简约信息多态位点，对应的氨基酸序列有41个氨基酸变异位点．根据Kimura 2参数构建的邻接树(NJ tree)和最大简约树(MP tree)都显示同样的结果：7种石首鱼类构成一个单系群．皮氏叫姑鱼位于单系群的基部，且与其他石首鱼分离时间很早；大黄鱼和棘头梅童鱼亲缘关系最近。并与钩牙皇石首鱼和波纹短须石首鱼构成姐妹群．黄姑鱼和鱿鱼也接近树的基部．     

节旋藻(螺旋藻)高分子量DNA的两种制备方法

DNA的简便高效制备方法是研究基因结构、功能及开展其它各项研究的基础。首次报道了针对节旋藻的结构和组成特性而建立的制备节旋藻高分子量DNA的两种方法。其中第一个方法是常规方法，可大量提取纯度较高、分子量达50kb的节旋藻DNA，可用于构建节旋藻质粒库、Southern杂交和PCR操作等；第2种方法是用脉冲电场凝胶电泳分离DNA片段，制备的DNA片段达数百kb，可用于构建节旋藻噬菌体库、粘粒库、BAC库等，从而为构建节旋藻物理图谱，定位克隆基因奠定基础。     

DNA adducts in mussels and fish exposed to bulky genotoxic compounds

Biological and procedural factors can influence DNA adduct detection in aquatic organisms. Among them, functional structure and metabolic traits represent major biological determinants for adducts formed by lipophilic pro-mutagenic contaminants. In detecting DNA adducts through the 32P-postlabelling assay, efficiency in DNA purification, digestion, labelling, as well as adduct enrichment and quantification may explain differences between independent studies. Reference DNA adducts have been used to verify some 32P-postlabelling aspects. Data obtained for mussels and fish treated with benzo[a]pyrene (B[a]P) and environmentally exposed to genotoxins confirm the above assertions. Although the 32P-postlabelling assay cannot be proposed for routine biomonitoring it appears a reliable and very sensitive index of exposure to genotoxic pollutants in both fish and mollusks.     

Identification of Porphyra lines using computerized DNA fingerprinting

ImpIONPorghyra is one of the most important rnarine a1gae with glObal distribution and importanterenomic value. AIthOtJgh the yield of POrPhpo is lower than that of kelp, the output valueof Porghpp occupies the first place in rnarine algae in China. The traditional taxonomy ishanly had on the morpbolOgical characteristics, such as the morpbobeical traits size, rnar-gin celIs and the number of repnductive cells. However, most of morPhobeical traits are af:fected by environrnntal factOrs …     

卵磷脂对花尾胡椒401幼鱼谷肤甘肤一硫一转移酶，谷肤甘肤过氧化物酶和DNA完整性的影响

采用不同卵磷脂添加量的配合饲料投喂花尾胡椒鲷(Plectorhyncchus cinctus）幼鱼，同步测定幼鱼的谷胱甘肽-硫-转移酶和谷胱甘肽过氧化物酶活性以及DNA完整程度。结果表明，谷胱甘肽-硫-转移酶和谷胱甘肽过氧化物酶活性随着饲料中卵磷脂含量的增加而提高，而DNA单链断裂程度随着饲料中卵磷脂含量的增加而减少。这提示卵磷脂能够提高鱼体的抗氧化防御系统的机能。     

福建太平洋牡蛎种群微卫星DNA分析

本文采用Ucdcg153、157、202微卫星引物对福建两个太平洋牡蛎(学名为长牡蛎Crassostrea gigas)养殖种群进行扩增分析和序列测定.与采自漳浦旧镇的近江牡蛎(C. ariakensis)比较,前者对以上三种引物全部呈阳性反应,后者只对Ucdcg157显阳性.与Genebank提供的相关序列比较,福建太平洋牡蛎与Genebank样品应属同源,其中漳浦霞美和厦门白礁的样品则可能代表同一种群的两个衍生品系.本项调查结果同时显示,近亲繁殖的育苗方式已经导致福建太平洋牡蛎种群裂化;任其发展不利于维护良种优势.本次采集的样品中未发现显示葡萄牙牡蛎、熊本牡蛎和美洲牡蛎微卫星特征的个体.     

镉致鲫(Carassius auratus)外周血单个核细胞DNA损伤与增殖抑制

采用体内注射染镉的方法进行镉诱导鲫外周血单个核细胞(PBMC)DNA损伤与增殖抑制相关性的研究。将鲫(400g／尾)驯养4周后进行随机分组，每组5尾，以Cdh浓度1．25、2．50和3．75mg／kg腹腔注射染鲫，以生理盐水腹腔注射鲫为对照，染镉后0、3、5、7、10和14天取无菌抗凝鲫血，经淋巴细胞分离液离心分离获取PBMC，用单细胞凝胶电泳法检测PBMC的DNA损伤，用^3H-胸腺嘧啶脱氧核苷掺入法检测PBMC的增殖。结果表明，3天时各染镉组DNA迁移度增加，5天时继续加大并于7天时达到峰值，10天和14天时呈现逐渐减小的趋势。1．25mg／kg组与对照组在不同时间放射性活度(咖m)的差异均无显著性；0天和3天时各染镉组与对照组咖m的差异均无显著性；5天时2．50和3．75mg／kg组dpm明显下降，7天和10天时dpm与5天时基本相同，14天时dpm呈上升趋势。镉诱导DNA损伤与其抑制PBMC增殖相比，作用时间短且浓度低，初步推测镉诱导的DNA损伤是镉抑制PBMC增殖的重要机制之一。     

乐清湾泥蚶血细胞周期和DNA含量

用流式细胞仪测定乐清湾泥蚶血细胞DNA含量，得出组方图中只有一个峰（G0/G1），表明了乐清湾泥蚶血液不存在合成期（S）、合成后期（G2）和分裂期（M）细胞，血细胞已失去分裂功能，不存在周期现象，以小鸡血细胞做标准对照物（DNA含量以2.3pg/N)，测得乐清湾泥蚶血细胞DNA含量为3.08pg/N。     

Assessing DNA damage in cnidarians using the Comet assay

The assessment of DNA damage by the Comet assay has been described as a useful non-specific general biomarker of stress in many marine organisms. In field situations it has successfully been employed to distinguish between reference and polluted sites and in the laboratory it has been widely used as a mechanistic tool to determine pollutant effects and mechanisms of DNA damage. To date a wide range of marine vertebrates and invertebrates have been used, however, the usefulness of this assay as a biomarker in cnidarians has not yet been assessed. The aims of this study were to optimize the Comet assay for cnidarian cells and to assess its utility for detecting genotoxic damage in these cells. Cells were isolated from the North American pacific coast temperate sea anemone Anthopleura elegantissima using a non-enzymatic dissociation procedure and viability was determined to be in excess of 90%. Cells were incubated either with (1 h acute exposures) hydrogen peroxide (H(2)O(2)), ethylmethanesulphonate (EMS) or benzo(a)pyrene (B[a]P). In comparison to other marine species, anemone cells exhibited high control or background levels of DNA strand breaks. Despite this, however, we observed dose responses for each of the study chemicals with no reduction in cell viability. This study demonstrates that anemone cells respond to known DNA damaging agents, including B[a]P which requires metabolism to exert its genotoxic effect, and that the Comet assay may prove to be a useful biomarker of stress in cnidarian species.