Human gephyrin is encompassed within giant functional noncoding yin-yang sequences
Nature Communications, ISSN: 2041-1723, Vol: 6, Issue: 1, Page: 6534
2015
- 10Citations
- 137Usage
- 39Captures
- 13Mentions
Metric Options: CountsSelecting the 1-year or 3-year option will change the metrics count to percentiles, illustrating how an article or review compares to other articles or reviews within the selected time period in the same journal. Selecting the 1-year option compares the metrics against other articles/reviews that were also published in the same calendar year. Selecting the 3-year option compares the metrics against other articles/reviews that were also published in the same calendar year plus the two years prior.
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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.
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Metrics Details
- Citations10
- Citation Indexes10
- CrossRef10
- 10
- Usage137
- Downloads127
- Abstract Views10
- Captures39
- Readers39
- 39
- Mentions13
- News Mentions9
- 9
- References4
- 4
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Article Description
Gephyrin is a highly conserved gene that is vital for the organization of proteins at inhibitory receptors, molybdenum cofactor biosynthesis and other diverse functions. Its specific function is intricately regulated and its aberrant activities have been observed for a number of human diseases. Here we report a remarkable yin-yang haplotype pattern encompassing gephyrin. Yin-yang haplotypes arise when a stretch of DNA evolves to present two disparate forms that bear differing states for nucleotide variations along their lengths. The gephyrin yin-yang pair consists of 284 divergent nucleotide states and both variants vary drastically from their mutual ancestral haplotype, suggesting rapid evolution. Several independent lines of evidence indicate strong positive selection on the region and suggest these high-frequency haplotypes represent two distinct functional mechanisms. This discovery holds potential to deepen our understanding of variable human-specific regulation of gephyrin while providing clues for rapid evolutionary events and allelic migrations buried within human history.
Bibliographic Details
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=84925743623&origin=inward; http://dx.doi.org/10.1038/ncomms7534; http://www.ncbi.nlm.nih.gov/pubmed/25813846; https://www.nature.com/articles/ncomms7534; https://irl.umsl.edu/cmpsci-faculty/34; https://irl.umsl.edu/cgi/viewcontent.cgi?article=1046&context=cmpsci-faculty; https://digitalcommons.wustl.edu/open_access_pubs/4342; https://digitalcommons.wustl.edu/cgi/viewcontent.cgi?article=5346&context=open_access_pubs; https://dx.doi.org/10.1038/ncomms7534; http://www.nature.com/ncomms/2015/150327/ncomms7534/full/ncomms7534.html; http://www.nature.com/doifinder/10.1038/ncomms7534; http://www.nature.com/articles/ncomms7534.pdf; http://www.nature.com/articles/ncomms7534
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