Cargando…

CRISPR/Cas9-based genetic screen of SCNT-reprogramming resistant genes identifies critical genes for male germ cell development in mice

Male germ cells undergo complex developmental processes eventually producing spermatozoa through spermatogenesis, although the molecular mechanisms remain largely elusive. We have previously identified somatic cell nuclear transfer-reprogramming resistant genes (SRRGs) that are highly enriched for g...

Descripción completa

Detalles Bibliográficos
Autores principales:	Akter, Most Sumona, Hada, Masashi, Shikata, Daiki, Watanabe, Gen, Ogura, Atsuo, Matoba, Shogo
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Nature Publishing Group UK 2021
Materias:	Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8322354/ https://www.ncbi.nlm.nih.gov/pubmed/34326397 http://dx.doi.org/10.1038/s41598-021-94851-9

Ejemplares similares

Suppression of endogenous retroviral enhancers in mouse embryos derived from somatic cell nuclear transfer
por: Shikata, Daiki, et al.
Publicado: (2022)

Highly rigid H3.1/H3.2–H3K9me3 domains set a barrier for cell fate reprogramming in trophoblast stem cells
por: Hada, Masashi, et al.
Publicado: (2022)

Easy and quick (EQ) sperm freezing method for urgent preservation of mouse strains
por: Mochida, Keiji, et al.
Publicado: (2021)

Aberrant DNA methylation reprogramming in bovine SCNT preimplantation embryos
por: Zhang, Sheng, et al.
Publicado: (2016)

Enhancement of Chromatin and Epigenetic Reprogramming in Porcine SCNT Embryos—Progresses and Perspectives
por: Glanzner, Werner Giehl, et al.
Publicado: (2022)

Synthetic CRISPR-Cas gene activators for transcriptional reprogramming in bacteria
por: Dong, Chen, et al.
Publicado: (2018)

Generation of chimeric mice with spermatozoa fully derived from embryonic stem cells using a triple-target CRISPR method for Nanos3
por: Miura, Kento, et al.
Publicado: (2020)

CRISPR/Cas9-mediated genome editing in wild-derived mice: generation of tamed wild-derived strains by mutation of the a (nonagouti) gene
por: Hirose, Michiko, et al.
Publicado: (2017)

Regeneration of spermatogenesis by mouse germ cell transplantation into allogeneic and xenogeneic testis primordia or organoids
por: Kanatsu-Shinohara, Mito, et al.
Publicado: (2022)

Somatic Donor Cell Type Correlates with Embryonic, but Not Extra-Embryonic, Gene Expression in Postimplantation Cloned Embryos
por: Hirasawa, Ryutaro, et al.
Publicado: (2013)

Long non-coding RNAs potentially function synergistically in the cellular reprogramming of SCNT embryos
por: Wu, Fengrui, et al.
Publicado: (2018)

Germ cell depletion in recipient testis has adverse effects on spermatogenesis in orthotopically transplanted testis pieces via retinoic acid insufficiency
por: Tsuchimoto, Akihiro, et al.
Publicado: (2020)

Author Correction: Synthetic CRISPR-Cas gene activators for transcriptional reprogramming in bacteria
por: Dong, Chen, et al.
Publicado: (2018)

Oxamflatin Significantly Improves Nuclear Reprogramming, Blastocyst Quality, and In Vitro Development of Bovine SCNT Embryos
por: Su, Jianmin, et al.
Publicado: (2011)

Dnmt1s in donor cells is a barrier to SCNT-mediated DNA methylation reprogramming in pigs
por: Song, Xuexiong, et al.
Publicado: (2017)

Characterization of DNA Methylation Patterns and Mining of Epigenetic Markers During Genomic Reprogramming in SCNT Embryos
por: Cao, Pengbo, et al.
Publicado: (2020)

Simultaneous Inhibition of Histone Deacetylases and RNA Synthesis Enables Totipotency Reprogramming in Pig SCNT Embryos
por: de Macedo, Mariana Priotto, et al.
Publicado: (2022)

Choosing a culture medium for SCNT and iSCNT reconstructed embryos: from domestic to wildlife species
por: Cordova, A., et al.
Publicado: (2017)

Oocytes Selected Using BCB Staining Enhance Nuclear Reprogramming and the In Vivo Development of SCNT Embryos in Cattle
por: Su, Jianmin, et al.
Publicado: (2012)

Pregnancy and Neonatal Care of SCNT Animals
por: Chavatte-Palmer, Pascale, et al.
Publicado: (2014)

Single-step generation of rabbits carrying a targeted allele of the tyrosinase gene using CRISPR/Cas9
por: Honda, Arata, et al.
Publicado: (2014)

Sperm-borne miR-449b influences cleavage, epigenetic reprogramming and apoptosis of SCNT embryos in bovine
por: Wang, Mengyun, et al.
Publicado: (2017)

Epigenetic reprogramming, gene expression and in vitro development of porcine SCNT embryos are significantly improved by a histone deacetylase inhibitor—m-carboxycinnamic acid bishydroxamide (CBHA)
por: Song, Yuran, et al.
Publicado: (2014)

Analysis of Endoplasmic Reticulum (ER) Stress Induced during Somatic Cell Nuclear Transfer (SCNT) Process in Porcine SCNT Embryos
por: Lee, Hwa-Yeon, et al.
Publicado: (2018)

Gene and mutation independent therapy via CRISPR-Cas9 mediated cellular reprogramming in rod photoreceptors
por: Zhu, Jie, et al.
Publicado: (2017)

CRISPR/Cas9 mediated chicken Stra8 gene knockout and inhibition of male germ cell differentiation
por: Zhang, Yani, et al.
Publicado: (2017)

RNA-Seq Profiling of Intact and Enucleated Oocyte SCNT Embryos Reveals the Role of Pig Oocyte Nucleus in Somatic Reprogramming
por: Bai, Lin, et al.
Publicado: (2016)

Loss of H3K27me3 imprinting in the Sfmbt2 miRNA cluster causes enlargement of cloned mouse placentas
por: Inoue, Kimiko, et al.
Publicado: (2020)

Epigenetic manipulation to improve mouse SCNT embryonic development
por: Li, Yamei, et al.
Publicado: (2022)

Reprogramming MHC specificity by CRISPR-Cas9-assisted cassette exchange
por: Kelton, William, et al.
Publicado: (2017)

Cell Reprogramming With CRISPR/Cas9 Based Transcriptional Regulation Systems
por: Shakirova, Ksenia M., et al.
Publicado: (2020)

Reprogramming Microbial CO(2)-Metabolizing Chassis With CRISPR-Cas Systems
por: Yu, Hai-Yan, et al.
Publicado: (2022)

In Vivo Genetic Manipulation of Spermatogonial Stem Cells and Their Microenvironment by Adeno-Associated Viruses
por: Watanabe, Satoshi, et al.
Publicado: (2018)

Novel HDAd/EBV Reprogramming Vector and Highly Efficient Ad/CRISPR-Cas Sickle Cell Disease Gene Correction
por: Li, Chao, et al.
Publicado: (2016)

Cellular Reprogramming, Genome Editing, and Alternative CRISPR Cas9 Technologies for Precise Gene Therapy of Duchenne Muscular Dystrophy
por: Gee, Peter, et al.
Publicado: (2017)

Modernising autism spectrum disorder model engineering and treatment via CRISPR-Cas9: A gene reprogramming approach
por: Sandhu, Arushi, et al.
Publicado: (2023)

Control of gene expression by CRISPR-Cas systems
por: Bikard, David, et al.
Publicado: (2013)

2-Cell-like Cells: An Avenue for Improving SCNT Efficiency
por: Fu, Bo, et al.
Publicado: (2022)

CRISPRe: An innate transcriptional enhancer for endogenous genes in CRISPR-Cas immunity
por: Li, Dan, et al.
Publicado: (2023)

Not all predicted CRISPR–Cas systems are equal: isolated cas genes and classes of CRISPR like elements
por: Zhang, Quan, et al.
Publicado: (2017)

Cannot write session to /tmp/vufind_sessions/sess_5mmkt8nf16kur0sfrd1jnmuksp