寄生云杉树蜂的枝跗瘿蜂一新种(膜翅目:瘿蜂总科:枝跗瘿蜂科)

枝跗瘿蜂科(Ibahidae)是个小科,所有种类均寄生蛀干害虫树蜂科(Siricidae)的幼虫。我国大陆的本科种类由杨忠岐1991年首次作了报道。现记述采自祁连山林区的另1新种。该种寄生于为害青海云杉(Picea crassifolia Kom.)的黄肩长尾树蜂(Xeris spec-trum spectrum)等树蜂的幼虫。新种的模式标本保存于西北林学院天敌昆虫研究室。至此,我国大陆共有本科种类3种,加上台湾的1个种,我国共有4种:     

Does alternative exon usage contribute to serotonin receptor heterogeneity?

We have previously isolated serotonin 5-HT_1C receptor cDNA clones. In contrast to most other receptors coupled to GTP binding proteins, the 5-HT_1C receptor gene contains several introns in its coding region. A similar exon-intron distribution is found in the 5-HT₂ receptor gene. The presence of large introns tempted us to test whether exchange of exons contributes to serotonin receptor heterogeneity. Therefore, blots with RNAs from different regions of the brain and brain slices were hybridized in situ with probes representing individual exons. We did not find any evidence for the exchange of exons which should result in an unequal distribution of hybridization signals found with the exon-specific probes. With the methodology used we should be able to see differential splicing in the form where individual exons are used alternatively resulting in mRNAs coding for different serotonin receptor types. We would not, however, see if a given exon can be modified by the alternative use of several splice-junctions.     

绿褶托菇在我国首次发现

本文报道我国蘑菇科Agaricaceae的一个新记录种——绿褶托菇Clarkeinda trachodes (Berk.)Singer,该种所隶属的绿褶托菇属Clarkeinda O. Kuntze现知是个分布于热带亚洲的单型属。     

云南羯布罗香树脂的化学成分

从云南产羯布罗香(Dipterocarpus tubinatus Gaertn. f.)树脂中分离得到6个三萜化合物,鉴定为羟基达玛烯酮—Ⅱ(hydroxydammarenone-Ⅱ,达玛烯二醇—Ⅱ(dammarenediol—Ⅱ),白桦脂酸(betulonk acid),亚细亚酸(asiatic acid),3,23-O-异丙叉亚细亚酸(3,23-O-isopropylidene asiatic acid)和崩大碗酸(madasiatic acid)。其中崩大碗酸系首次从龙脑香科树脂中分离得到。     

国产五种菊属植物的核型研究

本文对国产5种菊属植物的核型进行了研究,结果为:D. indicum 2n=2x=18=16m 2st,2n=4x=36=28m 6sm 2st;D. lavandulifolium 2n=2x=18=14m 4sm,2n=4x=36=28m 6sm 2st;D. lavandulifolium var.seticuspe 2n=2x=18=12m 6sm;D. chanetii 2n=4x=36=20m 14sm 2st,2n=6x=54=38m 14sm 2st;D. potentilloides2n=2x=18=14m 2sm 2st;D. vestitum 2n=6x=54=38m 16sm.核型分析的结果表明,本文所研究类群中出现的多倍体多为异源多倍体;根据对核型资料、形态特征及地理分布特点的综合分析,作者认为多倍化是菊属野生种进行的主要途径。     

Epithelio--mesenchymal interactions are critical for Quox 7 expression and membrane bone differentiation in the neural crest derived mandibular mesenchyme.

In higher vertebrates, branchial arch mesenchyme (ectomesenchyme) is derived from the cephalic neural crest. The ectomesenchyme of the mandibular arch yields the Meckel's cartilage and several membrane bones. We previously reported the isolation of a quail homeobox gene, Quox 7. In common with its mouse counterpart Hox 7, Quox 7 is highly expressed in the medioventral part of the mandibular arch and later in the precursor cells of the membrane bones. Since bone differentiation from ectomesenchyme is strictly dependent upon a signal provided by the mandibular epithelium, we decided to see whether the regulation of Quox 7 gene activity might be correlated with epithelio--mesenchymal interactions. Quox 7 expression was studied in E3 mandibular ectomesenchyme cultured in vitro or grafted on the chick chorioallantoic membrane either alone or recombined with the homotopic and heterotopic epithelia. We found that Quox 7 mRNA was undetectable after 48 h in cultures of mesenchyme alone while it remained abundant in non-cartilaginous tissue of the mandibular arch ectomesenchyme recombined with its own epithelium. The signal provided by the mandibular epithelium for Quox 7 expression can also arise from various heterotopic epithelia, e.g. of dorsal or ventral body wall and of limb bud. Thus the effect of the epithelium on Quox 7 expression in mesenchymal cells strictly parallels that on bone formation. These results strongly suggest that the epithelio-mesenchymal interactions have an essential role on the regulation of Quox 7 gene, the product of which seems to be, in turn, necessary for the execution of the skeletal developmental program in the facial area.     

Solution conformation of an oligonucleotide containing a G.G mismatch determined by nuclear magnetic resonance and molecular mechanics.

We have determined by two-dimensional nuclear magnetic resonance studies and molecular mechanics calculations the three dimensional solution structure of the non-selfcomplementary oligonucleotide, d(GAGGAGGCACG). d(CGTGCGTCCTC) in which the central base pair is G.G. This is the first structural determination of a G.G mismatch in a oligonucleotide. Two dimensional nuclear magnetic resonance spectra show that the bases of the mismatched pair are stacked into the helix and that the helix adopts a classical B-DNA form. Spectra of the exchangeable protons show that the two guanosines are base paired via their imino protons. For the non-exchangeable protons and for some of the exchangeable protons nuclear Overhauser enhancement build up curves at short mixing times have been measured. These give 84 proton-proton distances which are sensitive to the helix conformation. One of the guanosines adopts a normal anti conformation while the other is syn or close to syn. All non-terminal sugars are C2' endo. These data sets were incorporated into the refinement of the oligonucleotide structure by molecular mechanics calculations. The G.G mismatch shows a symmetrical base pairing structure. Although the mismatch is very bulky many of its features are close to that of normal B-DNA. The mismatch induces a small lateral shift in the helix axis and the sum of the helical twist above and below the mismatch is close to that of B-DNA.     

The solution structure of a DNA hairpin containing a loop of three thymidines determined by nuclear magnetic resonance and molecular mechanics.

We have determined by two-dimensional nuclear magnetic resonance studies and molecular mechanics calculations the three-dimensional solution structure of a 21 residue oligonucleotide capable of forming a hairpin structure with a loop of three thymidine residues. This structure is in equilibrium with a duplex form. At 33 degrees C, low ionic strength and in the presence of MgCl2 the hairpin form dominates in solution. Six Watson-Crick base pairs are formed topped by the loop structure. The residues 1-3 and 18-21 are not complementary and form dangling ends. Distance constraints have been derived from nuclear Overhauser enhancement measurements. These, together with molecular mechanics calculations, have been used to determine the structure. We do not observe stacking of thymidine residues either over the 3' or the 5' end of the stem.     

Synthesis and physicochemical properties of oligonucleotides built with either alpha-L or beta-L nucleotides units and covalently linked to an acridine derivative.

Modified deoxynucleosides 2'-deoxy-beta-L-uridine, beta-L-thymidine, alpha-L-thymidine, 2'-deoxy-beta-L-adenosine and 2'-deoxy-alpha-L-adenosine were synthesized and assembled as homooligomers, respectively: octa-beta-L-deoxyuridylates, octa beta-L and alpha-L-thymidylates and tetra beta-L and alpha-L-deoxyadenylates. These unnatural oligomers were then substituted with an acridine derivative. The binding studies of these modified oligonucleotides with D-ribo- and D-deoxyribopolynucleotides were carried out by absorption spectroscopy. While beta-L-d(Up)8m5Acr, beta-L-(Tp)8m5Acr, alpha-L-(Tp)8m5Acr did not interact with poly(rA) and poly(dA), beta-L-d(Ap)4m5Acr and alpha-L-d(Ap)4m5Acr did form double and triple helices with poly(rU) and poly(dT), respectively. Their stability towards nuclease digestion was studied through comparison with that of octa-beta-D-thymidylate and tetra beta-D-deoxyadenylate covalently linked to an acridine derivative. One endonuclease (nuclease P1 from Penicillium citrinum) and two exonucleases (a 3'-exonuclease from Crotalus durissus venom and a 5'-exonuclease extracted from calf thymus) were employed. beta-L- and alpha-L-oligomers demonstrate a high resistance toward nuclease digestion.