Induction of germ cell-deficiency in grass puffer by dead end 1 gene knockdown for use as a recipient in surrogate production of tiger puffer

Aquaculture ◽  
2020 ◽  
Vol 526 ◽  
pp. 735385 ◽  
Author(s):  
Hiroyuki Yoshikawa ◽  
Yasuko Ino ◽  
Kenta Kishimoto ◽  
Hayato Koyakumaru ◽  
Taiju Saito ◽  
...  
2019 ◽  
Vol 9 (1) ◽  
Author(s):  
Ana Carina Nogueira Vasconcelos ◽  
Danilo Pedro Streit ◽  
Anna Octavera ◽  
Misako Miwa ◽  
Naoki Kabeya ◽  
...  

2014 ◽  
Vol 144 (3-4) ◽  
pp. 129-137 ◽  
Author(s):  
Adrijana Škugor ◽  
Helge Tveiten ◽  
Aleksei Krasnov ◽  
Øivind Andersen

Nature ◽  
2005 ◽  
Vol 435 (7040) ◽  
pp. 360-364 ◽  
Author(s):  
Kirsten K. Youngren ◽  
Douglas Coveney ◽  
Xiaoning Peng ◽  
Chitralekha Bhattacharya ◽  
Laura S. Schmidt ◽  
...  

2006 ◽  
Vol 291 (1) ◽  
pp. 1-11 ◽  
Author(s):  
Katja Horvay ◽  
Maike Claußen ◽  
Mathias Katzer ◽  
Jobst Landgrebe ◽  
Tomas Pieler

Animals ◽  
2019 ◽  
Vol 9 (4) ◽  
pp. 174 ◽  
Author(s):  
Abdul Rasheed Baloch ◽  
Roman Franěk ◽  
Tomáš Tichopád ◽  
Michaela Fučíková ◽  
Marek Rodina ◽  
...  

Sturgeons also known as living fossils are facing threats to their survival due to overfishing and interference in natural habitats. Sterlet (Acipenser ruthenus) due to its rapid reproductive cycle and small body size can be used as a sterile host for surrogate production for late maturing and large sturgeon species. Dead end protein (dnd1) is essential for migration of Primordial Germ Cells (PGCs), the origin of all germ cells in developing embryos. Knockout or knockdown of dnd1 can be done in order to mismigrate PGCs. Previously we have used MO and UV for the aforementioned purpose, and in our present study we have used CRISPR/Cas9 technology to knockout dnd1. No or a smaller number of PGCs were detected in crispants, and we also observed malformations in some CRISPR/Cas9 injected embryos. Furthermore, we compared three established methods to achieve sterility in sterlet, and we found higher embryo survival and hatching rates in CRISPR/Cas9, UV and MO, respectively.


2017 ◽  
Vol 43 (6) ◽  
pp. 704-715.e5 ◽  
Author(s):  
Theresa Gross-Thebing ◽  
Sargon Yigit ◽  
Jana Pfeiffer ◽  
Michal Reichman-Fried ◽  
Jan Bandemer ◽  
...  

2019 ◽  
Author(s):  
Lene Kleppe ◽  
Rolf Brudvik Edvardsen ◽  
Tomasz Furmanek ◽  
Eva Andersson ◽  
Kai Ove Skaftnesmo ◽  
...  

Abstract Background Sustainability challenges are currently hampering an increase in salmon production. Using sterile salmon can solve problems with precocious puberty and genetic introgression from farmed escapees to wild populations. Recently sterile salmon was produced by knocking out the germ cell-specific dead end (dnd). Several approaches may be applied to inhibit Dnd function, including gene knockout, knockdown or immunization. Since it is challenging to develop a successful treatment against a gene product already existing in the body, alternative targets are being explored. Germ cells are surrounded by, and dependent on, gonadal somatic cells. Targeting genes essential for the survival of gonadal somatic cells may be good alternative targets for sterility treatments. Our aim was to identify and characterize novel germ cell and gonadal somatic factors in Atlantic salmon. Results We have for the first time analysed RNA-sequencing data from germ cell-free (GCF)/dnd knockout and wild type (WT) salmon testis and searched for genes preferentially expressed in either germ cells or gonadal somatic cells. To exclude genes with extra-gonadal expression, our dataset was merged with available multi-tissue transcriptome data. We identified 389 gonad specific genes, of which 194 were preferentially expressed within germ cells, and 11 were confined to gonadal somatic cells. Interestingly, 5 of the 11 gonadal somatic transcripts represented genes encoding secreted TGF-β factors; gsdf, inha, nodal and two bmp6-like genes, all representative vaccine targets. Of these, gsdf and inha had the highest transcript levels. Expression of gsdf and inha was further confirmed to be gonad specific, and their spatial expression was restricted to granulosa and Sertoli cells of the ovary and testis, respectively. Finally, we show that inha expression increases with puberty in both ovary and testis tissue, while gsdf expression does not change or decreases during puberty in ovary and testis tissue, respectively. Conclusions This study contributes with transcriptome data on salmon testis tissue with and without germ cells. We provide a list of novel and known germ cell- and gonad somatic specific transcripts, and show that the expression of two highly active gonadal somatic secreted TGF-β factors, gsdf and inha, are located within granulosa and Sertoli cells.


2015 ◽  
Vol 41 (2) ◽  
pp. 561-571 ◽  
Author(s):  
Jundan Duan ◽  
Gongqing Feng ◽  
Pei Chang ◽  
Xueyan Zhang ◽  
Qingchun Zhou ◽  
...  

2016 ◽  
Vol 28 (12) ◽  
pp. 2051 ◽  
Author(s):  
Ido Bar ◽  
Andre Smith ◽  
Erin Bubner ◽  
Goro Yoshizaki ◽  
Yutaka Takeuchi ◽  
...  

Germ cell transplantation is an innovative technology for the production of interspecies surrogates, capable of facilitating easier and more economical management of large-bodied broodstock, such as the bluefin tuna. The present study explored the suitability of yellowtail kingfish (Seriola lalandi) as a surrogate host for transplanted southern bluefin tuna (Thunnus maccoyii) spermatogonial cells to produce tuna donor-derived gametes upon sexual maturity. Germ cell populations in testes of donor T. maccoyii males were described using basic histology and the molecular markers vasa and dead-end genes. The peripheral area of the testis was found to contain the highest proportions of dead-end-expressing transplantable Type A spermatogonia. T. maccoyii Type A spermatogonia-enriched preparations were transplanted into the coelomic cavity of 6–10-day-old post-hatch S. lalandi larvae. Fluorescence microscopy and polymerase chain reaction analysis detected the presence of tuna cells in the gonads of the transplanted kingfish fingerlings at 18, 28, 39 and 75 days after transplantation, indicating that the transplanted cells migrated to the genital ridge and had colonised the developing gonad. T. maccoyii germ cell-derived DNA or RNA was not detected at later stages, suggesting that the donor cells were not maintained in the hosts’ gonads.


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