{"title":"On the fine structure and composition of the nuclear envelope.","authors":"R W MERRIAM","doi":"10.1083/jcb.11.3.559","DOIUrl":null,"url":null,"abstract":"<p><p>Nuclei from nearly ripe eggs of Rana pipiens were isolated and cleaned in 0.1 M KCl. The whole nucleus was then digested to various degrees with ribonuclease or trypsin, followed by washing and fixation in either osmium tetroxide or potassium permanganate. The nuclear envelope was dissected off, placed on a grid, air dried, and compared with undigested controls in the electron microscope. Some envelopes were dehydrated, embedded in methacrylate, and sectioned. Annuli around \"pores\" are composed of a substance or substances, at least partially fibrillar, which is preserved by osmium but lost during permanganate fixation. Material within the \"pores\" is also preserved by osmium but partially lost after permanganate. No evidence of granules or tubules in the annuli was found in air dried mounts although a granular appearance could be seen in tangentially oriented thin sections. Thin sections of isolated envelopes give evidence of diffuse material within the \"pores\" as well as a more condensed diaphragm across their waists. In whole mounts of the envelope the total density within \"pores\" is relatively constant from \"pore\" to \"pore.\" All material within \"pores,\" including the condensed diaphragm, is removable by trypsin digestion. Wispy material from the \"pore\" structure projects into the nucleus and annular material extends into the cytoplasm. Both annular and diaphragm materials remain with the envelope when it is isolated and are thus considered a part of its structure, not merely evidences of material passing through. There is no evidence of ribonuclease-removable material in any part of the \"pore\" complex.</p>","PeriodicalId":22618,"journal":{"name":"The Journal of Biophysical and Biochemical Cytology","volume":"11 ","pages":"559-70"},"PeriodicalIF":0.0000,"publicationDate":"1961-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1083/jcb.11.3.559","citationCount":"75","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"The Journal of Biophysical and Biochemical Cytology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1083/jcb.11.3.559","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 75
Abstract
Nuclei from nearly ripe eggs of Rana pipiens were isolated and cleaned in 0.1 M KCl. The whole nucleus was then digested to various degrees with ribonuclease or trypsin, followed by washing and fixation in either osmium tetroxide or potassium permanganate. The nuclear envelope was dissected off, placed on a grid, air dried, and compared with undigested controls in the electron microscope. Some envelopes were dehydrated, embedded in methacrylate, and sectioned. Annuli around "pores" are composed of a substance or substances, at least partially fibrillar, which is preserved by osmium but lost during permanganate fixation. Material within the "pores" is also preserved by osmium but partially lost after permanganate. No evidence of granules or tubules in the annuli was found in air dried mounts although a granular appearance could be seen in tangentially oriented thin sections. Thin sections of isolated envelopes give evidence of diffuse material within the "pores" as well as a more condensed diaphragm across their waists. In whole mounts of the envelope the total density within "pores" is relatively constant from "pore" to "pore." All material within "pores," including the condensed diaphragm, is removable by trypsin digestion. Wispy material from the "pore" structure projects into the nucleus and annular material extends into the cytoplasm. Both annular and diaphragm materials remain with the envelope when it is isolated and are thus considered a part of its structure, not merely evidences of material passing through. There is no evidence of ribonuclease-removable material in any part of the "pore" complex.
用0.1 M KCl对近成熟的库蚊卵进行核分离和清洗。然后用核糖核酸酶或胰蛋白酶对整个细胞核进行不同程度的消化,然后在四氧化二锇或高锰酸钾中洗涤和固定。核膜被解剖,放在网格上,风干,并在电子显微镜下与未消化的对照进行比较。一些信封脱水,包在甲基丙烯酸酯中,切片。“孔”周围的环空由一种或多种物质组成,至少部分是纤维状的,由锇保存,但在高锰酸盐固定过程中丢失。“孔隙”内的物质也被锇保存,但在高锰酸盐后部分丢失。在风干标本中未发现环空中颗粒或小管的证据,尽管在切向取向的薄切片中可以看到颗粒状外观。孤立包膜的薄片表明,“毛孔”内有弥漫性物质,腰上也有更密集的隔膜。在包膜的整个层中,“孔”内的总密度从“孔”到“孔”是相对恒定的。“毛孔”内的所有物质,包括压缩的隔膜,都可以通过胰蛋白酶消化去除。丝状物质从“孔”结构投射到细胞核中,环状物质延伸到细胞质中。环形材料和膜片材料在被隔离时仍留在外壳内,因此被认为是其结构的一部分,而不仅仅是材料穿过的证据。在“孔”复合体的任何部分都没有核糖核酸可去除物质的证据。