Literature DB >> 826376

Analysis of chromatin-associated fiber arrays.

C D Laird, L E Wilkinson, V E Foe, W Y Chooi.   

Abstract

Electron microscopic examination of chromatin from embryonic nuclei of Oncopeltus fasciatus and Drosophila melanogaster reveals arrays of chromatin associated fibers. The lengths and spacings of these fibers were analyzed to provide a basis for defining and interpreting regions of transcriptionally active chromatin. The results of the analysis are consistent with the interpretation of some fibers as nascent RNA with associated protein (RNP). The chromatin segments underlying these fiber arrays were classified as ribosomal or non-ribosomal transcription units according to definitions and criteria described by Foe et al. (1976). Nascent fibers on active ribosomal transcription units were analyzed and compared for Drosophila melanogaster, Triturus viridescens, and Oncopeltus fasciatus. A common feature of the fiber patterns on ribosomal TUs is that origin-distal fibers exhibit greater length variability and a lower slope relative to proximal fibers. The region of increased variability in fiber lengths is correlated with the expected location of 28S ribosomal RNA sequences in the distal half of each ribosomal transcription unit. Because 28S ribosomal RNA appears to contain more extensive regions of base sequence complementarity, we suggest that the length of ribosomal RNP fibers is influenced under our spreading conditions by the secondary structure of the nascent RNA. In order to calculate the RNA content of RNP fibers, chromatin morphology was used to estimate lengths of transcribed DNA. The packing ratio of DNA in chromatin, which we express as the length of B-structure DNA divided by length of chromatin, is 1.1-1.2 and 1.6 for the DNA in active ribosomal and non-ribosomal chromatins, respectively. These DNA packing ratios are used to determine the extent to which nascent RNP fibers are shorter than the transcribed DNA (expressed as DNA/RNP length ratio). For non-ribosomal transcription units and for proximal fibers of ribosomal transcription units. DNA/RNP length ratios are relatively constant within each array. However, considerable variability in this ratio (4-23) is observed for different arrays of fibers. Possible sources of this variability are considered by comparing ratios derived from the presumably identical ribosomal transcription units. Further analysis of the morphology of nascent fibers may elucidate the contributions of proteins and successive RNA sequences to RNP structure.

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Year:  1976        PMID: 826376     DOI: 10.1007/BF00701357

Source DB:  PubMed          Journal:  Chromosoma        ISSN: 0009-5915            Impact factor:   4.316


  41 in total

1.  Acceleration of RNA renaturation by nucleic acid unwinding proteins.

Authors:  R L Karpel; D G Swistel; N S Miller; M E Geroch; C Lu; J R Fresco
Journal:  Brookhaven Symp Biol       Date:  1975-07

2.  Analysis of subunit organization in chicken erythrocyte chromatin.

Authors:  B R Shaw; T M Herman; R T Kovacic; G S Beaudreau; K E Van Holde
Journal:  Proc Natl Acad Sci U S A       Date:  1976-02       Impact factor: 11.205

3.  The transcriptional organization of the ribosomal RNA genes in mouse L cells.

Authors:  P B Hackett; W Sauerbier
Journal:  J Mol Biol       Date:  1975-01-25       Impact factor: 5.469

4.  Morphological studies of transcription.

Authors:  O L Miller; A H Bakken
Journal:  Acta Endocrinol Suppl (Copenh)       Date:  1972

5.  Secondary structure maps of ribosomal RNA and DNA. I. Processing of Xenopus laevis ribosomal RNA and structure of single-stranded ribosomal DNA.

Authors:  P K Wellauer; I B Dawid
Journal:  J Mol Biol       Date:  1974-10-25       Impact factor: 5.469

6.  Secondary structure maps of ribosomal RNA. II. Processing of mouse L-cell ribosomal RNA and variations in the processing pathway.

Authors:  P K Wellauer; I B Dawid; D E Kelley; R P Perry
Journal:  J Mol Biol       Date:  1974-10-25       Impact factor: 5.469

7.  Chromatin sub-structure. The digestion of chromatin DNA at regularly spaced sites by a nuclear deoxyribonuclease.

Authors:  D R Hewish; L A Burgoyne
Journal:  Biochem Biophys Res Commun       Date:  1973-05-15       Impact factor: 3.575

8.  Lampbrush chromosomes in spermatocytes of Chironomus.

Authors:  H G Keyl
Journal:  Chromosoma       Date:  1975       Impact factor: 4.316

9.  Ultrastructural patterns of RNA synthesis during early embryogenesis of Drosophila melanogaster.

Authors:  S L McKnight; O L Miller
Journal:  Cell       Date:  1976-06       Impact factor: 41.582

10.  Structural repeating units in chromatin. I. Evidence for their general occurrence.

Authors:  C L Woodcock; J P Safer; J E Stanchfield
Journal:  Exp Cell Res       Date:  1976-01       Impact factor: 3.905

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  34 in total

1.  HnRNP core proteins: synthesis, turnover and intracellular distribution.

Authors:  T Martin; R Jones; P Billings
Journal:  Mol Biol Rep       Date:  1979-05-31       Impact factor: 2.316

2.  Lengths and patterns of transcriptional units in the amplified nucleoli of oocytes of Xenopus laevis.

Authors:  U Scheer; M F Trendelenburg; G Krohne; W W Franke
Journal:  Chromosoma       Date:  1977-03-16       Impact factor: 4.316

3.  RNA synthesis in isolated polytene nuclei from Chironomus tentans.

Authors:  H Hameister
Journal:  Chromosoma       Date:  1977-07-08       Impact factor: 4.316

4.  Equations describing the effects of the transient stability of subpopulations of nascent hnRNAs on the kinetics of turnover of hnRNA.

Authors:  K C Kleene
Journal:  Biochem J       Date:  1986-02-01       Impact factor: 3.857

5.  A quantitative electron microscopic analysis of transcription in sea urchin embryos.

Authors:  S Busby; A Bakken
Journal:  Chromosoma       Date:  1979-03-12       Impact factor: 4.316

6.  Structure of nuclear ribonucleoprotein: heterogeneous nuclear RNA is complexed with a major sextet of proteins in vivo.

Authors:  I V Economidis; T Pederson
Journal:  Proc Natl Acad Sci U S A       Date:  1983-03       Impact factor: 11.205

7.  Morphology of transcription units in Drosophila melanogaster.

Authors:  C D Laird; W Y Chooi
Journal:  Chromosoma       Date:  1976-10-28       Impact factor: 4.316

8.  Transcription mapping of the Escherichia coli chromosome by electron microscopy.

Authors:  S L French; O L Miller
Journal:  J Bacteriol       Date:  1989-08       Impact factor: 3.490

9.  Lengths of transcribed rDNA repeating units in spermatocytes of Drosophila hydei: only genes without an intervening sequence are expressed.

Authors:  K H Glätzer
Journal:  Chromosoma       Date:  1979-11       Impact factor: 4.316

10.  Ultrastructural analysis of polytene chromatin of Drosophila melanogaster reveals clusters of tightly linked co-expressed genes.

Authors:  E J Hager; O L Miller
Journal:  Chromosoma       Date:  1991-03       Impact factor: 4.316

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