THE DIAMETERS OF FROZEN-HYDRATED CHROMATIN FIBERS INCREASE WITH DNA LINKER LENGTH - EVIDENCE IN SUPPORT OF VARIABLE DIAMETER MODELS FOR CHROMATIN

被引:55
作者
ATHEY, BD [1 ]
SMITH, MF [1 ]
RANKERT, DA [1 ]
WILLIAMS, SP [1 ]
LANGMORE, JP [1 ]
机构
[1] UNIV MICHIGAN,DEPT BIOL SCI,ANN ARBOR,MI 48109
关键词
D O I
10.1083/jcb.111.3.795
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The diameters of chromatin fibers from Thyone briareus (sea cucumber) sperm (DNA linker length, n = 87 bp) and Necturus maculosus (mudpuppy) erythrocytes (n = 48 bp) were investigated. Soluble fibers were frozen into vitrified aqueous solutions of physiological ionic strength (124 mM), imaged by cryo-EM, and measured interactively using quantitative computer image-processing techniques. Frozenhydrated Thyone and Necturus fibers had significantly different mean diameters of 43.5 nm (SD = 4.2 nm; SEM = 0.61 nm) and 32.0 nm (SD = 3.0 nm; SEM = 0.36 nm), respectively. Evaluation of previously published EM data shows that the diameters of chromatin from a large number of sources are proportional to linker length. In addition, the inherent variability in fiber diameter suggests a relationship between fiber structure and the heterogeneity of linker length. The cryo-EM data were in quantitative agreement with space-filling double-helical crossed-linker models of Thyone and Necturus chromatin. The data, however, do not support solenoid or twisted-ribbon models for chromatin that specify a constant 30 nm diameter. To reconcile the concept of solenoidal packing with the data, we propose a variable-diameter solid-solenoid model with a fiber diameter that increases with linker length. In principle, each of the variable diameter models for chromatin can be reconciled with local variations in linker length.
引用
收藏
页码:795 / 806
页数:12
相关论文
共 72 条
[1]   THE DIAMETER OF CHROMATIN FIBERS DEPENDS ON LINKER LENGTH [J].
ALEGRE, C ;
SUBIRANA, JA .
CHROMOSOMA, 1989, 98 (01) :77-80
[2]   HIGHER-ORDER STRUCTURE IN A SHORT REPEAT LENGTH CHROMATIN [J].
ALLAN, J ;
RAU, DC ;
HARBORNE, N ;
GOULD, H .
JOURNAL OF CELL BIOLOGY, 1984, 98 (04) :1320-1327
[3]   TECHNIQUES FOR THE PRESERVATION OF 3-DIMENSIONAL STRUCTURE IN PREPARING SPECIMENS FOR THE ELECTRON MICROSCOPE [J].
ANDERSON, TF .
TRANSACTIONS OF THE NEW YORK ACADEMY OF SCIENCES, 1951, 13 (04) :130-134
[4]  
BEVINGTON PR, 1969, DATA REDUCTION ERROR, P119
[5]   THE SUPERSTRUCTURE OF CHROMATIN AND ITS CONDENSATION MECHANISM .2. THEORETICAL-ANALYSIS OF THE X-RAY-SCATTERING PATTERNS AND MODEL-CALCULATIONS [J].
BORDAS, J ;
PEREZGRAU, L ;
KOCH, MHJ ;
VEGA, MC ;
NAVE, C .
EUROPEAN BIOPHYSICS JOURNAL WITH BIOPHYSICS LETTERS, 1986, 13 (03) :175-185
[6]   THE SUPERSTRUCTURE OF CHROMATIN AND ITS CONDENSATION MECHANISM .1. SYNCHROTRON RADIATION X-RAY-SCATTERING RESULTS [J].
BORDAS, J ;
PEREZGRAU, L ;
KOCH, MHJ ;
VEGA, MC ;
NAVE, C .
EUROPEAN BIOPHYSICS JOURNAL WITH BIOPHYSICS LETTERS, 1986, 13 (03) :157-173
[8]  
CRANEROBINSON C, 1984, COMMENTS MOL CELL BI, V2, P219
[9]   FINE-STRUCTURE OF CHROMATIN AS VISUALIZED IN THIN-SECTIONS WITH THE GAUTIER SELECTIVE STAIN FOR DNA [J].
DERENZINI, M .
JOURNAL OF ULTRASTRUCTURE RESEARCH, 1979, 69 (02) :239-248
[10]  
DIMITROV SI, 1988, J BIOMOL STRUCT DYN, V2, P1135