Cataloging Human PRDM9 Allelic Variation Using Long-Read Sequencing Reveals PRDM9 Population Specificity and Two Distinct Groupings of Related Alleles
The PRDM9 protein determines sites of meiotic recombination in humans by directing meiotic DNA double-strand breaks to specific loci. Targeting specificity is encoded by a long array of C2H2 zinc fingers that bind to DNA. This zinc finger array is hypervariable, and the resulting alleles each have a...
Guardado en:
Autores principales: | Benjamin Alleva, Kevin Brick, Florencia Pratto, Mini Huang, Rafael Daniel Camerini-Otero |
---|---|
Formato: | article |
Lenguaje: | EN |
Publicado: |
Frontiers Media S.A.
2021
|
Materias: | |
Acceso en línea: | https://doaj.org/article/475ec1506de04b55a5624ce8c30a7799 |
Etiquetas: |
Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
|
Ejemplares similares
-
PRDM12 in Health and Diseases
por: Monica Rienzo, et al.
Publicado: (2021) -
Characterization of Prdm9 in equids and sterility in mules.
por: Cynthia C Steiner, et al.
Publicado: (2013) -
Discovery of a chemical probe for PRDM9
por: Abdellah Allali-Hassani, et al.
Publicado: (2019) -
ATM and PRDM9 regulate SPO11-bound recombination intermediates during meiosis
por: Jacob Paiano, et al.
Publicado: (2020) -
An Induced Mutation in HvRECQL4 Increases the Overall Recombination and Restores Fertility in a Barley HvMLH3 Mutant Background
por: Mikel Arrieta, et al.
Publicado: (2021)