杉木、台湾杉、香杉逐步判别分析

通过对杉木、台湾杉、香杉２２个种源的叶长、叶宽、叶厚、维管束的宽与厚、栅栏组织厚、机械组织厚、表皮厚和气孔数等９个叶性状进行逐步判别分析,选取栅栏组织厚（Ｘ＿６）、叶长（Ｘ＿１）和叶厚（Ｘ＿３）三个重要因子,建立优化判别方程：Ｆ＿１（台湾杉）＝－２３５．８７１４＋１７．３１０４Ｘ＿６＋２６．３５８７Ｘ＿１＋５．９０４６Ｘ＿３Ｆ＿２（杉木）＝－５６４．９２５９＋７８．４２５４Ｘ＿６＋９３．１９２３Ｘ＿１＋０．６２９５Ｘ＿３Ｆ＿３（香杉）＝－３４９．４２０５＋６４．１９２６Ｘ＿６＋６２．６４７９Ｘ＿１＋０．８９６９Ｘ＿３定量地区分这三个树种,旨在对逐步判别分析法在树种分类上的应用进行探讨。     

Expression and characterization of virus-like particles containing rubella virus structural proteins.

Rubella virus (RV) virions contain two envelope glycoproteins (E1 and E2) and a capsid protein (C). Noninfectious RV-like particles (VLPs) containing three structural proteins were expressed in a BHK cell line (BHK-24S) by using an inducible promoter. These VLPs were found to resemble RV virons in terms of their size, their morphology, and some biological activities. In immunoblotting studies, VLPs were found to bind similarly to native RV virions with 10 of a panel of 12 RV-specific murine monoclonal antibodies. Immunization of mice with VLPs induced specific antibody responses against RV structural proteins as well as virus-neutralizing and hemagglutination-inhibiting antibodies. After immunization of mice with VLPs, in vitro challenge of isolated lymphocytes with inactivated RV and individual RV structural proteins stimulated proliferation. Our data suggest the possibility of using VLPs as immunogens for serodiagnostic assays and RV vaccines.     

磁水对蕃茄酯酶同工酶的影响

蕃茄（ＬｙｃｏｐｅｒｓｉｃｏｍｅｓｃｕｌｅｎｔｕｍＭｉｌｌ）在各生长发育期酯酶同工酶谱带无明显变化,但经磁水处理后各生长发育阶段功能叶中酯酶同工酶酶谱及磷素含量与对照组相比存在显著差异,且具有酶谱负极端带数增加,正极端带数减少的趋势。总磷含量测定结果表明处理组均比对照组显著提高。这些变化在磁水处理著前后代中不存在,故认为磁水只是致使非编码顺序局部复制引起ＤＮＡ分子高级结构改变或是通过活化调节基因来调控酯酶同工酶,活化磷代谢,达到促进生长和增产的效果,而并非导致可遗传变异的结果。     

黄麻栽培种圆果种×长果种的种间杂交研究

１９８９—１９９１年对黄麻栽培种圆果种（Ｃｏｒｃｈｏｒｕｓｃａｐｓｕｌａｒｉｓ）和长果种（Ｃ．ｏｌｉｔ－ｏｒｉｕｓ）选用了具有不同茎色和腋芽性状的材料做了６个组合,获得１３４株杂种Ｆ＿１苗。但苗株发根不良,在移栽后两周陆续死亡,最后幸存ＲＲ－５×（ＢＬ×７７－１９）Ｆ＿１组合中两株植株并开花、结果。Ｆ＿１均有腋芽,表现为父本的性状;花果形状偏向母本;茎色红同双亲。这两株的Ｆ＿２,茎色和腋芽性状分离成４种表现型：红茎或青茎有腋芽及红茎或青茎无腋芽。其中红茎有腋芽的生长较快。对种间杂交技术、亲本间的花粉与柱头亲和性、杂交花的胚珠受精情况及染色体构型等方面也作了观察、研究。     

重组人IL6／2融合蛋白对6.5Gy照射小鼠造血功能恢复的影响

观察了ｈＦＰＩＬ６／２对６．５Ｇｙγ线照射ＮＩＨ小鼠第１０天造血功能恢复的影响。结果表明：照射小鼠连续４ｄ给予ｈＦＰＩＬ６／２２５０μｇ·ｋｇ－１·ｄ－１,其脾重、ＣＦＵ－８、骨髓有核细胞数及ＣＭ－ＣＦＵ分别比对照组增加５９．０％、２７８．５％、５７．９％和１３８．２％,统计学处理均有显著差异;对此四项指标的改善也明显优于２５μｇ组。另外,２５０μｇ剂量组小鼠外周血象３０ｄ的动态观察结果表明,ｈＦＰＩＬ６／２不但能明显提高红细胞和血红蛋白的最低值,而且能使血小板的恢复提前。提示ｈＦＰＩＬ６／２在促进血小板生成和促进红系造血方面可能具有良好的应用前景。     

单纯疱疹病毒通用及Ⅱ型特异性DNA探针的制备及应用研究

单纯疱疹病毒（ＨＳＶ）Ⅰ型及Ⅱ型之间有很多共同抗原,能引起血清学交叉反应,鉴别诊断比较困难。本实验利用重组ＤＮＡ技术,将部分ＨＳＶ－２ＤＮＡ的ＰｓｔＩ片段克隆到载体质粒ＰＳＫ中,并筛选出两个重组质粒（Ｐ和Ｐ）只与ＨＳＶ－２反应,与ＨＳＶ－１不反应,这两个重组质粒中所含的ＨＳＶ－２ＤＮＡ片段大小分别是３．１和４．３ｋｂ,另外,还筛选了一个重组质粒（ＰＨＳＶ２－１,含５．８ｋｂＨＳＶ－２ＤＮＡ片段）与ＨＳＶ－１和ＨＳＶ－２均反应。将４．３ｋｂ的片段用光生物素标记后作为探针检测了１５９份人阴道拭子,其中２３份样品呈阳性反应,其余均为阴性,从２３份阳性样品中挑选１２价涂片用间接荧光抗体法检测也都呈阳性反应,随机挑选的几份杂交反应阴性样品在间接荧光试验中也是阴性。本实验制备的ＨＳＶ通用及ＨＳＶ－２型特异性探针将比常规的血清学方法诊断和鉴别ＨＳＶ－１和ＨＳＶ－２感染更为可靠。     

穴位激光照射对兔子宫类固醇激素受体的影响

对兔用Ｈｅ－Ｎｅ激光照射穴位,照射外生殖器,用类固醇激素受体测定法测定子宫雌二醇受体（ＥＲ）和孕酮受体（ＰＲ）含量。照射穴位后部分实验组的ＥＲ和ＰＲ浓度上升,与正常对照组相比较有显著或极显著差别（Ｐ＜０．０５,Ｐ＜０．０１）,ＥＲ提高１．７－３．２倍,ＰＲ提高２．７－３．７倍。实验结果提示激光可通过类固醇激素受体浓度的提高,在受体水平上影响机体代谢。     

Evidence for heterogeneity in facioscapulohumeral muscular dystrophy (FSHD)

Facioscapulohumeral muscular dystrophy (FSHD) is a slowly progressive primary disease of muscle which is usually inherited as an autosomal dominant disorder. FSHD has been localized to the long arm of chromosome 4, specifically to the 4q3.5-qter region. Initially published linkage studies showed no evidence for heterogeneity in FSHD. In the present study we have examined individuals in seven FSHD families. Two-point lod scores show significant evidence for linkage for D4S163 (lod score 3.04 at recombination fraction .21) and D4S139 (lod score 3.84 at recombination fraction .20). D4S171 also gave a positive score (lod score 2.56 at recombination fraction .24). Significant evidence for heterogeneity was found for each of the three markers. Multipoint linkage analysis in this region resulted in a peak multipoint lod score of 6.47. The multipoint analysis supported the two-point studies with odds of 20:1 showing linkage and heterogeneity over linkage and homogeneity. Five of the seven families gave a posterior probability of >95% of being of the linked type, while two families appeared unlinked to this region of 4q (P < .01%). Individuals in the two unlinked families met the clinical criteria for the diagnosis of FSHD, including facial weakness, clavicular flattening, scapula winging, proximal muscle weakness, and myopathic changes on muscle biopsies without inflammatory or mitochondrial pathology. This study demonstrates genetic heterogeneity in FSHD and has important implications for both genetic counseling and the elucidation of the etiology of FSHD.