1973
DOI: 10.1139/o73-065
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Transcription of Satellite DNA in Mouse L-cells

Abstract: Mouse L-cells contain RNA capable of hybridizing with mouse satellite DNA on nitrocellulose membranes and of competing for hybridizing sites on satellite DNA with transcript of satellite DNA prepared in vitro. RNA prepared from either whole cells or from the cytoplasm includes a fraction hybridizing with satellite DNA. That from whole cells has a half-life of 17 min, whereas that from cytoplasm is stable.

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Cited by 27 publications
(14 citation statements)
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“…These tandem repeats have historically been called satellite DNA because their densities often differ from bulk chromatin during centrifugation. As early as the 1960s and 1970s, evidence for transcription of mouse satellites was reported (18,32), as was the presence of RNA in kinetochores of both plants and animals (7,10,56). Detailed characterization of the RNA was not possible in these early studies because of the limitations of the experimental methods available.…”
Section: Usage Of the Terms Centromere And Pericentromerementioning
confidence: 99%
“…These tandem repeats have historically been called satellite DNA because their densities often differ from bulk chromatin during centrifugation. As early as the 1960s and 1970s, evidence for transcription of mouse satellites was reported (18,32), as was the presence of RNA in kinetochores of both plants and animals (7,10,56). Detailed characterization of the RNA was not possible in these early studies because of the limitations of the experimental methods available.…”
Section: Usage Of the Terms Centromere And Pericentromerementioning
confidence: 99%
“…Despite identification of satellite DNA transcription in mouse as early as the late 60s (Harel et al, 1968;Cohen et al, 1973), the structure of CT and PCT transcripts remains poorly characterized. Indeed, the repetitive nature of CT and PCT regions adds to the difficulty of their analysis.…”
Section: Where and When Are Ct And Pct Sequences Expressed?mentioning
confidence: 99%
“…Prior to PCR, success in identifying such transcripts depended upon methodology, cell type or developmental stage. [38][39][40][41][42][43][44] After the advent of reverse-transcriptase PCR (RT)-PCR, such transcripts were identified in a number of mouse cell lines, [30][31][32]45,46 in some human cell lines under stressed conditions, 47,48 and in a few human cancer cell lines. 49 However, considering that pericentric heterochromatin comprises a large percentage of genomic DNA (5-10% in mice) yet detection of transcripts frequently requires sensitive methods, transcription is expected to be relatively rare or at only a small number of sites.…”
Section: Mammalian Heterochromatin Transcription Has Been Difficult Tmentioning
confidence: 99%