Chromatin fine structure of the histone gene complex of Drosophila melanogaster.

We have used salt extractions of nuclei and long agarose gels to dissect the chromatin fine structure of the histone gene repeat of Drosophila melanogaster. Extraction of nuclei with 0.35 M KCl removes many non-histone chromosomal proteins but does not significantly disturb the overall nucleosome arrangement of the repeat unit. After extraction of nuclei with 0.55 M KCl, which also removes histone Hl, the basic arrangement of nucleosome core particles in the repeat unit is not greatly disturbed and the exposed DNA segments near the 5' ends of the histone genes are also retained. Extraction of nuclei with 0.75 M or higher KCl concentrations causes extensive nucleosome sliding and rearrangement with accompanying changes in the nucleoprotein organization of the histone gene complex and loss of the 5' hypersensitive sites. Our results indicate that the histone gene repeat displays a highly organized chromatin structure in vivo.     

Chromatin structural elements and chromosomal translocations in leukemia

Recurring chromosome abnormalities are strongly associated with certain subtypes of leukemia, lymphoma and sarcomas. More recently, their potential involvement in carcinomas, i.e. prostate cancer, has been recognized. They are among the most important factors in determining disease prognosis, and in many cases, identification of these chromosome abnormalities is crucial in selecting appropriate treatment protocols. Chromosome translocations are frequently observed in both de novo and therapy-related acute myeloid leukemia (AML) and myelodysplastic syndromes (MDS). The mechanisms that result in such chromosome translocations in leukemia and other cancers are largely unknown. Genomic breakpoints in all the common chromosome translocations in leukemia, including t(4;11), t(9;11), t(8;21), inv(16), t(15;17), t(12;21), t(1;19) and t(9;22), have been cloned. Genomic breakpoints tend to cluster in certain intronic regions of the relevant genes including MLL, AF4, AF9, AML1, ETO, CBFB, MYHI1, PML, RARA, TEL, E2A, PBX1, BCR and ABL. However, whereas the genomic breakpoints in MLL tend to cluster in the 5' portion of the 8.3 kb breakpoint cluster region (BCR) in de novo and adult patients and in the 3' portion in infant leukemia patients and t-AML patients, those in both the AML1 and ETO genes occur in the same clustered regions in both de novo and t-AML patients. These differences may reflect differences in the mechanisms involved in the formation of the translocations. Specific chromatin structural elements, such as in vivo topoisomerase II (topo II) cleavage sites, DNase I hypersensitive sites and scaffold attachment regions (SARs) have been mapped in the breakpoint regions of the relevant genes. Strong in vivo topo II cleavage sites and DNase I hypersensitive sites often co-localize with each other and also with many of the BCRs in most of these genes, whereas SARs are associated with BCRs in MLL, AF4, AF9, AML1, ETO and ABL, but not in the BCR gene. In addition, the BCRs in MLL, AML1 and ETO have the lowest free energy level for unwinding double strand DNA. Virtually all chromosome translocations in leukemia that have been analyzed to date show no consistent homologous sequences at the breakpoints, whereas a strong non-homologous end joining (NHEJ) repair signature exists at all of these chromosome translocation breakpoint junctions; this includes small deletions and duplications in each breakpoint, and micro-homologies and non-template insertions at genomic junctions of each chromosome translocation. Surprisingly, the size of these deletions and duplications in the same translocation is much larger in de novo leukemia than in therapy-related leukemia. We propose a non-homologous chromosome recombination model as one of the mechanisms that results in chromosome translocations in leukemia. The topo II cleavage sites at open chromatin regions (DNase I hypersensitive sites), SARs or the regions with low energy level are vulnerable to certain genotoxic or other agents and become the initial breakage sites, which are followed by an excision end joining repair process.     

我国的十种两栖动物

中国有２８０种左右两栖动物,分隶３目１１科。介绍１０个物种的形态特征和部分习性及分布等。     

隐种及其在两栖动物中的研究进展

近年来,由于分子生物学的迅猛发展,物种内隐藏的生物多样性越来越多地被发现,由此引发的隐种问题也备受关注。隐种的存在对现有的生物多样性评估提出了挑战。在实践上,隐种的界定对于自然资源的保护和管理具有重要意义。两栖动物由于迁移能力较弱,通常具有较强的遗传分化,因而可能包含较丰富的隐种多样性。简述了隐种的概念和形成机制,归纳了国内外两栖类动物中隐种的研究进展,并着重介绍了界定两栖动物隐种的研究方法,最后,对今后两栖动物隐种的研究作了简要展望。我国两栖动物资源丰富,并具有独特的地形和气候特点,对这些物种遗传多样性和系统地理学的研究亟待开展。     

Ultimobranchial gland structure in some species of squamata

Calotes versicolor has single gland on the left side in neck region, just anterior to heart, while Ptyas mucosus and Bungarus caeruleus have 2 equal-sized glands located in the thyro-thymic region. The gland was spheroidal and measured 0.5 to 1.5 mm in diameter. Size of the gland varied individually in relation to the body size. The gland was composed of cell masses and follicles, and was well vascularized. Histology of the gland showed marked individual variation. Ciliated and goblet cells were present.     

Ultrastructural studies of oogenesis in some european amphibians

Summary Oogenesis was studied in adult Triturus vulgaris (Urodela) with the electron microscope. The oocytes investigated ranged between 50 m and 1600 m in diameter.Two types of yolk platelet formation were found. Since both types involve the incorporation of high numbers of pinocytotic vesicles they are believed to be of an extraoocytic origin. On the basis of the order of their appearance they were named primary and secondary yolk.Five different types of vesicles were found, which participate in a variety of activities, such as yolk formation and the formation of the Golgi apparatus. They originate from four different sources, namely the nuclear membrane, the cytoplasm in connection with ribosome-like particles, the Golgi apparatus and the plasma membrane through pinocytosis. The results obtained were discussed especially with respect to differences found between the anura and the urodela, such as the presence or absence of cortical granules or equivalent structures.The authors wish to thank Prof. Dr. K.S. Ludwig for his valuable criticism and encouragement during the course of this study, Messrs. H. Boffin, C. Evers and Miss D. Lovri for their capable technical assistance.