Literature DB >> 2725493

Nonrandom distribution of long mono- and dinucleotide repeats in Drosophila chromosomes: correlations with dosage compensation, heterochromatin, and recombination.

K Lowenhaupt1, A Rich, M L Pardue.   

Abstract

Long stretches of (dC-dA)n.(dT-dG)n, abbreviated CA/TG, have a distinctive distribution on Drosophila chromosomes (M.L. Pardue, K. Lowenhaupt, A. Rich, and A. Nordheim, EMBO J. 6:1781-1789, 1987). The distribution of CA/TG suggests a correlation with the overall transcriptional activity of chromosomal regions and with the ability to undergo meiotic recombination. These correlations are conserved among Drosophila species and may indicate one or more chromosomal functions. To test the generality of these findings, we analyzed the distribution of the rest of the six possible mono- and dinucleotide repeats (A/T, C/G, AT/AT, CA/TG, CT/AG, and CG/CG). All but CG/CG were present at significant levels in the genomes of the six Drosophila species studied; however, A/T levels were an order of magnitude lower than those of the other sequences. Data base analyses suggested that the same sequences are present in other eucaryotes. Like CA/TG, both CT/AG and C/G showed increased levels on dosage-compensating chromosomes; however, the individual sites clearly differed for each sequence. In contrast, A/T and AT/AT, although present in Drosophila DNA, could not be detected in situ in polytene chromosomes. We also used in situ hybridization to analyze the neo-Y chromosome of Drosophila miranda, an ancestral autosome that has become attached to the Y chromosome and is now partially heterochromatic. The neo-Y has acquired repeated DNA sequences; we found that the added sequences are as devoid of mono- and dinucleotide repeats as other heterochromatin. The distribution and function of these sequences are likely to result from both their repetitious nature and base contents.

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Year:  1989        PMID: 2725493      PMCID: PMC362708          DOI: 10.1128/mcb.9.3.1173-1182.1989

Source DB:  PubMed          Journal:  Mol Cell Biol        ISSN: 0270-7306            Impact factor:   4.272


  28 in total

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5.  Chromosomal basis of dosage compensation in Drosophila VIII. Faster replication and hyperactivity of both arms of the X-chromosome in males of Drosophila pseudoobscura and their possible significance.

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6.  Telomere regions in Drosophila share complex DNA sequences with pericentric heterochromatin.

Authors:  B S Young; A Pession; K L Traverse; C French; M L Pardue
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Authors:  D Treco; N Arnheim
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8.  Possible structures of homopurine-homopyrimidine S1-hypersensitive sites.

Authors:  C R Cantor; A Efstratiadis
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9.  Incomplete dosage compensation in an evolving Drosophila sex chromosome.

Authors:  E Strobel; C Pelling; N Arnheim
Journal:  Proc Natl Acad Sci U S A       Date:  1978-02       Impact factor: 11.205

10.  A novel repeated element with Z-DNA-forming potential is widely found in evolutionarily diverse eukaryotic genomes.

Authors:  H Hamada; M G Petrino; T Kakunaga
Journal:  Proc Natl Acad Sci U S A       Date:  1982-11       Impact factor: 11.205

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  40 in total

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Authors:  J Locke; L Podemski; N Aippersbach; H Kemp; R Hodgetts
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3.  Chromosomal detection of simple sequence repeats (SSRs) using nondenaturing FISH (ND-FISH).

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Review 4.  Heterochromatin: junk or collectors item?

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5.  Molecular and cytogenetic analysis of the heterochromatin-euchromatin junction region of the Drosophila melanogaster X chromosome using cloned DNA sequences.

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6.  Synaptonemal complexes from DNase-treated rat pachytene chromosomes contain (GT)n and LINE/SINE sequences.

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Review 7.  Revisiting junk DNA.

Authors:  E Zuckerkandl
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Review 8.  Potential genetic functions of tandem repeated DNA sequence blocks in the human genome are based on a highly conserved "chromatin folding code".

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Journal:  Hum Genet       Date:  1990-03       Impact factor: 4.132

Review 9.  A lot about a little dot - lessons learned from Drosophila melanogaster chromosome 4.

Authors:  Nicole C Riddle; Christopher D Shaffer; Sarah C R Elgin
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10.  Word frequency analysis reveals enrichment of dinucleotide repeats on the human X chromosome and [GATA]n in the X escape region.

Authors:  John A McNeil; Kelly P Smith; Lisa L Hall; Jeanne B Lawrence
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