scholarly journals Identification and characterization of primordial germ cells in a vocal learning Neoaves species, the zebra finch

2019 ◽  
Vol 33 (12) ◽  
pp. 13825-13836 ◽  
Author(s):  
Kyung Min Jung ◽  
Young Min Kim ◽  
Anna L. Keyte ◽  
Matthew T. Biegler ◽  
Deivendran Rengaraj ◽  
...  
2020 ◽  
Author(s):  
Ivana Gessara ◽  
Falk Dittrich ◽  
Moritz Hertel ◽  
Staffan Hildebrand ◽  
Alexander Pfeifer ◽  
...  

SUMARYThe ability to genetically manipulate organisms has led to significant insights in functional genomics in many species. In birds, manipulation of the genome is hindered by the inaccessibility of the one-cell embryo. During embryonic development, avian primordial germ cells (PGCs) migrate through the blood stream and reach the gonadal anlage; where they develop into mature germ cells. Here, we explored the use of PGCs to produce transgenic offspring in the zebra finch, which is a major animal model for sexual brain differentiation, vocal learning and vocal communication. Zebra finch PGCs (zfPGCs) obtained from embryonic blood significantly proliferated when cultured in an optimized culture medium and conserved the expression of germ and stem cell markers. Transduction of cultured zfPGCs with lentiviral vectors was highly efficient leading to strong expression of the enhanced green fluorescent protein (eGFP). Transduced zfPGCs were injected into the host embryo and transgenic songbirds were successfully generated.


2007 ◽  
Vol 210 (1) ◽  
pp. 98-111 ◽  
Author(s):  
Clara Armengol ◽  
Ana Carretero ◽  
Víctor Nacher ◽  
Jesús Ruberte ◽  
Marc Navarro

2019 ◽  
Vol 193 ◽  
pp. 192-204 ◽  
Author(s):  
Melissah Rowe ◽  
Sheri Skerget ◽  
Matthew A. Rosenow ◽  
Timothy L. Karr

Development ◽  
1977 ◽  
Vol 39 (1) ◽  
pp. 221-233
Author(s):  
Masami Wakahara

Larvae of Rana chensinensis developed from fertilized eggs which had been subjected to ultraviolet (u.v.) irradiation on their vegetal hemisphere at a dose of 20000 ergs/mm2 within 60 min of fertilization contained no primordial germ cells (PGCs) when examined histologically at the stage when the operculum was complete (8 days after fertilization at 18 °C, stage 25 according to Shumway, 1940). The morphogenetic ability of vegetal pole cytoplasm from non-irradiated eggs to establish the PGCs was tested by injecting some fractions of this cytoplasm into the vegetal hemisphere of u.v.-irradiated eggs. Crude homogenate of the vegetal pole cytoplasm without large yolk platelets was able to restore the PGCs when injected into u.v.-irradiated eggs, but a similar fraction from animal half cytoplasm had no ability to form PGCs. The ‘PGC-forming activity’ demonstrated in the crude homogenate of the vegetal pole cytoplasm was not abolished by dialysis, lyophilization and heating to 90 °C for 10 min. When the homogenate was fractionated by differential centrifugation in 0·25 M sucrose, the ‘PGC-forming activity’ was recovered mainly in the precipitate of 15000g for 30 min. The precipitate of 7000 g for 10 min had also a little ‘activity’. The possibility was discussed that the ‘PGC-forming activity’ demonstrated in the vegetal pole cytoplasm was associated with the germinal granules in the germ plasm rather than the mitochondria.


2018 ◽  
Vol 24 (5) ◽  
pp. 233-243 ◽  
Author(s):  
Maria Gomes Fernandes ◽  
Monika Bialecka ◽  
Daniela C F Salvatori ◽  
Susana M Chuva de Sousa Lopes

Stem Cells ◽  
2016 ◽  
Vol 34 (9) ◽  
pp. 2418-2428 ◽  
Author(s):  
C. Eguizabal ◽  
L. Herrera ◽  
L. De Oñate ◽  
N. Montserrat ◽  
P. Hajkova ◽  
...  

1985 ◽  
Vol 29 (2) ◽  
pp. 145-151 ◽  
Author(s):  
Horacio Merchant-Larios ◽  
Fela Mendlovic ◽  
Arturo Alvarez-Buylla

1996 ◽  
Vol 88 (1-2) ◽  
pp. 79-79
Author(s):  
Xavier VIGNON ◽  
Solange DELASALLE ◽  
Jacques FLÉCHON ◽  
Yasuhisa MATSUI

2017 ◽  
Vol 52 (2) ◽  
pp. 261-267 ◽  
Author(s):  
N.A. Volkova ◽  
◽  
V.A. Bagirov ◽  
E.K. Tomgorova ◽  
A.N. Vetokh ◽  
...  

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