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Primordial germ cell-mediated transgenesis and genome editing in birds.

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TLDR
A historical overview of avian PGCs and their application is introduced, including improved techniques and methodologies in the production of transgenic and genome-edited birds are introduced, and the future potential applications of transgenesis and genome editing in birds are discussed to provide opportunities and benefits for humans.
Abstract
Transgenesis and genome editing in birds are based on a unique germline transmission system using primordial germ cells (PGCs), which is quite different from the mammalian transgenic and genome editing system. PGCs are progenitor cells of gametes that can deliver genetic information to the next generation. Since avian PGCs were first discovered in nineteenth century, there have been numerous efforts to reveal their origin, specification, and unique migration pattern, and to improve germline transmission efficiency. Recent advances in the isolation and in vitro culture of avian PGCs with genetic manipulation and genome editing tools enable the development of valuable avian models that were unavailable before. However, many challenges remain in the production of transgenic and genome-edited birds, including the precise control of germline transmission, introduction of exogenous genes, and genome editing in PGCs. Therefore, establishing reliable germline-competent PGCs and applying precise genome editing systems are critical current issues in the production of avian models. Here, we introduce a historical overview of avian PGCs and their application, including improved techniques and methodologies in the production of transgenic and genome-edited birds, and we discuss the future potential applications of transgenic and genome-edited birds to provide opportunities and benefits for humans.

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Therapeutic genome editing: prospects and challenges

TL;DR: Current progress toward developing programmable nuclease–based therapies as well as future prospects and challenges are discussed.
Journal ArticleDOI

Manipulation of spermatogonial stem cells in livestock species.

TL;DR: The general aim of this review is to outline comprehensively the promising applications of SSC manipulation that could in the nearest future find practical application in livestock breeding.
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Germline engineering of the chicken genome using CRISPR/Cas9 by in vivo transfection of PGCs.

TL;DR: G germline targeting of the endogenous chicken Interferon Alpha and Beta Receptor Subunit 1 (IFNAR1) gene is reported by in vivo transgenic expression of the high-fidelity Cas9 and guide RNAs (gRNAs) in chickens.
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Current Approaches and Applications in Avian Genome Editing

TL;DR: The development of avian genome editing and scientific and industrial applications of GE avian species is described and direct injection of adenovirus into the avian blastoderm in the freshly laid eggs resulted in the production of germ-line chimera and GE offspring.
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Production of microhomologous-mediated site-specific integrated LacS gene cow using TALENs.

TL;DR: This study provides a new strategy to facilitate gene knock-ins in livestock using techniques that exhibit improved biosafety and intuitive methodologies and produces low-lactose cow.
References
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A programmable dual-RNA-guided DNA endonuclease in adaptive bacterial immunity.

TL;DR: This study reveals a family of endonucleases that use dual-RNAs for site-specific DNA cleavage and highlights the potential to exploit the system for RNA-programmable genome editing.
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A series of normal stages in the development of the chick embryo

TL;DR: In this article, a series of normal stages of the chick embryo is described in terms of the length of time of incubation, except for the first three days during which more detailed characteristics such as the number of somites are applied.
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CRISPR provides acquired resistance against viruses in prokaryotes

TL;DR: It is found that, after viral challenge, bacteria integrated new spacers derived from phage genomic sequences, and CRISPR provided resistance against phages, and resistance specificity is determined by spacer-phage sequence similarity.
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Cpf1 is a single RNA-guided endonuclease of a class 2 CRISPR-Cas system.

TL;DR: In this paper, the authors characterized Cpf1, a putative class 2 CRISPR effector, which is a single RNA-guided endonuclease lacking tracrRNA and utilizes a T-rich protospacer-adjacent motif.
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Programmable editing of a target base in genomic DNA without double-stranded DNA cleavage

TL;DR: E engineered fusions of CRISPR/Cas9 and a cytidine deaminase enzyme that retain the ability to be programmed with a guide RNA, do not induce dsDNA breaks, and mediate the direct conversion of cytidine to uridine, thereby effecting a C→T (or G→A) substitution.
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