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==Function==
==Function==
PRDM9 is thought to mediate the process of [[Recombination_hotspot|meiotic homologous recombination]].<ref name="pmid21460839">{{cite journal | author = Smagulova F, Gregoretti IV, Brick K, Khil P, Camerini-Otero RD, Petukhova GV | title = Genome-wide analysis reveals novel molecular features of mouse recombination hotspots | journal = Nature | volume = 472 | issue = 7343 | pages = 375–8 | year = 2011 | month = April | pmid = 21460839 | doi = 10.1038/nature09869 }}</ref>
PRDM9 is thought to mediate the process of [[Recombination_hotspot|meiotic homologous recombination]].<ref name="pmid21460839">{{cite journal | author = Smagulova F, Gregoretti IV, Brick K, Khil P, Camerini-Otero RD, Petukhova GV | title = Genome-wide analysis reveals novel molecular features of mouse recombination hotspots | journal = Nature | volume = 472 | issue = 7343 | pages = 375–8 |date=April 2011 | pmid = 21460839 | doi = 10.1038/nature09869 }}</ref>


==Notes==
==Notes==

Revision as of 19:55, 28 January 2014

Template:PBB

PR domain[note 1] zinc finger protein 9 is a protein that in humans is encoded by the Prdm9 gene.[1] The protein has histone H3(K4) trimethyltransferase activity, a KRAB domain, and a DNA-binding domain consisting of multiple tandem C2H2 zinc finger (ZF) domains.[2] PRDM9 specifically trimethylates 'Lys-4' of histone H3 during meiotic prophase and is essential for proper meiotic progression, but does not have the ability to mono- and dimethylate 'Lys-4' of histone H3. H3 'Lys-4' methylation represents a specific tag for epigenetic transcriptional activation which plays a central role in the transcriptional activation of genes during early meiotic prophase.

Function

PRDM9 is thought to mediate the process of meiotic homologous recombination.[3]

Notes

  1. ^ positive-regulatory domain

References

  1. ^ "Entrez Gene: PR domain containing 9".
  2. ^ Thomas JH, Emerson RO, Shendure J (2009). "Extraordinary molecular evolution in the PRDM9 fertility gene". PLoS ONE. 4 (12): e8505. doi:10.1371/journal.pone.0008505. PMC 2794550. PMID 20041164.{{cite journal}}: CS1 maint: multiple names: authors list (link) CS1 maint: unflagged free DOI (link)
  3. ^ Smagulova F, Gregoretti IV, Brick K, Khil P, Camerini-Otero RD, Petukhova GV (April 2011). "Genome-wide analysis reveals novel molecular features of mouse recombination hotspots". Nature. 472 (7343): 375–8. doi:10.1038/nature09869. PMID 21460839.{{cite journal}}: CS1 maint: multiple names: authors list (link)

Further reading

External links

This article incorporates text from the United States National Library of Medicine, which is in the public domain.