Curvature of mouse satellite DNA and condensation of heterochromatin
Cell, ISSN: 0092-8674, Vol: 50, Issue: 7, Page: 1101-1108
1987
- 184Citations
- 12Captures
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
Citation Benchmarking is provided by Scopus and SciVal and is different from the metrics context provided by PlumX Metrics.
Metrics Details
- Citations184
- Citation Indexes184
- 184
- CrossRef134
- Captures12
- Readers12
- 12
Article Description
Cloned, sequenced mouse satellite DNA exhibits properties characteristic of molecules that possess a stable curvature. Circularly permuted fragments containing the region predicted to bend were used to map the curvature relative to DNA sequence. The altered mobility of these fragments in polyacrylamide gels is reversed when gels are run in the presence of distamycin A, a drug that binds preferentially to AT-rich DNA. Treatment of living mouse cells with this drug dramatically reduces the condensation of centromeric heterochromatin, the exclusive location of satellite sequences. In situ hybridization of satellite probes to extended chromosomes at the electron microscope level shows that satellite does not comprise a single block but is distributed throughout the centromere region. Based on these experiments, we hypothesize that the structure of mouse satellite DNA is an important feature of centromeric heterochromatin condensation.
Bibliographic Details
http://www.sciencedirect.com/science/article/pii/0092867487901760; http://dx.doi.org/10.1016/0092-8674(87)90176-0; http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=0023664977&origin=inward; http://www.ncbi.nlm.nih.gov/pubmed/2441880; https://linkinghub.elsevier.com/retrieve/pii/0092867487901760; http://dx.doi.org/10.1016/0092-8674%2887%2990176-0; https://dx.doi.org/10.1016/0092-8674%2887%2990176-0
Elsevier BV
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