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湿态无活性染色质的超结构与染色体表面

Superstructures of wet inactive chromatin and the chromosome surface.

作者信息

Basu S

出版信息

J Supramol Struct. 1979;10(4):377-95. doi: 10.1002/jss.400100402.

Abstract

Superpacking of chromatin and the surface features of metaphase chromosomes have been studied by SiO replication of wet, unstained, and unfixed specimens in an exceedingly thin (less than or equal to nm) aqueous layer, keeping them wet. Hydrophilic Formvar substrates allow controlled thinning of the aqueous layer covering the wet specimens. Whole mounts of chromatin and chromosomes were prepared by applying a microsurface spreading method to swollen nuclei and mitotic cells at metaphase. The highest level of nucleosome folding of the inactive chromatin in chicken erythrocytes and rat liver nuclei is basically a second-order superhelical organization (width 150--200 nm, pitch distance 50--150 nm) of the elementary nucleosome filament. In unfavorable environments (as determined by ionic agents, fixative, and dehydrating agetns) this superstructure collapses into chains of superbeads and beads. Formalin (10%) apparently attacks at discrete sites of chromatin, which are then separated into superbeads. The latter consist of 4--6 nucleosomes and seemingly correspond to successive turns of an original solenoidal coil (width 30--35 nm), which forms the superhilical organization. When this organization is unfolded, eg, in 1--2 mM EDTA, DNAse-sensitive filaments (diameter 1.7 nm) are seen to be wrapped around the nucleosomes. The wet chromosomes in each metaphase spread are held to each other by smooth microtubular fibers, 20--20 nm in diameter. Before they enter into a chromsome, these fibers branch into 9--13 protofilaments, each 5 nm wide. The chromosome surface contains a dense distribution of subunits about 10--25 nm in diameter. This size distribution corresponds to that of nucleosomes and their superbeads. Distinct from this beaded chromosome surface are several smooth, 23--30-nm-diameter fibers, which are longitudinal at the centromere and seem to continue into the chromatid structure. The surface replicas of dried chromosomes do not show these features, which are revealed only in wet chromosomes.

摘要

通过在极薄(小于或等于纳米)的水层中对湿润、未染色且未固定的标本进行二氧化硅复制,研究了染色质的超紧密包装和中期染色体的表面特征,使标本保持湿润。亲水性福尔马林中膜底物可控制覆盖湿润标本的水层变薄。通过对肿胀的细胞核和中期有丝分裂细胞应用微表面铺展法制备染色质和染色体的整装标本。鸡红细胞和大鼠肝细胞核中无活性染色质的核小体折叠最高水平基本上是基本核小体细丝的二级超螺旋结构(宽度150 - 200纳米,螺距距离50 - 150纳米)。在不利环境中(由离子试剂、固定剂和脱水剂确定),这种超结构会塌陷成超珠链和珠链。10%的福尔马林显然攻击染色质的离散位点,然后将其分离成超珠。后者由4 - 6个核小体组成,似乎对应于原始螺线管线圈(宽度30 - 35纳米)的连续匝数,该线圈形成超螺旋结构。当这种结构展开时,例如在1 - 2 mM的EDTA中,可看到对DNA酶敏感的细丝(直径1.7纳米)缠绕在核小体周围。每个中期铺展中的湿润染色体通过直径为20 - 20纳米的光滑微管纤维相互连接。在它们进入染色体之前,这些纤维分支成9 - 13条原纤维,每条宽5纳米。染色体表面含有直径约10 - 25纳米的亚基密集分布。这种大小分布与核小体及其超珠的大小分布相对应。与这种珠状染色体表面不同的是几条光滑的、直径为23 - 30纳米的纤维,它们在着丝粒处纵向排列,似乎延续到染色单体结构中。干燥染色体的表面复制品没有显示出这些特征,这些特征仅在湿润染色体中才会显现。

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