Hatching gland development and hatching in zebrafish embryos: a role for zinc and its transporters Zip10 and Znt1a
Hatching gland development and hatching in zebrafish embryos: a role for zinc and its transporters Zip10 and Znt1a
Zinc transporters of the ZIP (Slc39, importers) and ZnT (Slc30, exporters) protein families have evolutionary conserved roles in biology. The aim of the present study was to explore the role of zinc, and zinc transporters Zip10 and Znt1a in zebrafish hatching gland development and larval hatching. In the study, knockdown of genes for Zip10 and Znt1a in zebrafish embryos was achieved using morpholino-modified oligonucleotides. A partial loss-of-function Znt1a mutant (Znt1asa17) allowed comparison with the Znt1a morphant. Free Zn2+ in embryos and apoptosis were investigated using fluorescent dyes whereas gene expression was investigated by whole-mount in situ hybridization (WISH). The results showed high levels of free Zn2+ in the hatching gland cells (HGC) along with abundant expression of zip10 and znt1a in normal embryo. Knockdown of zip10 reduced free Zn2+ in HGC, ceased their normal developmental apoptosis, and resulted in displacement and later disappearance of hatching glands and hatching enzymes he1a and catL1b, and inability to hatch. Conversely, knockdown of znt1a or the Znt1asa17 mutation accelerated hatching and coincided with high expression of hatching enzymes and free Zn2+ in the HGC. Thus, Zip10 and free Zn2+ in the HGC are required both for their development and function. This study also demonstrated the opposite functions of the two zinc transporters, ZIP10 and ZnT1 as well as shedding light on the role of Zn2+ in regulation of the human hatching enzyme homologue, ovastacin, which is activated by zinc and cleaves the zona pellucida protein, ZP2, to prevent polyspermy
698-705
Muraina, Issa A.
e52ee155-995b-4f85-aa5b-ff682978769d
Maret, Wolfgang
41845264-4c6c-4841-ae1e-a8b843c34ba4
Bury, Nic R.
696daba0-5cc9-444c-be9a-c678808712c6
Hogstrand, Christer
157377cc-b2e9-4931-8a88-0b8764362ee5
1 August 2020
Muraina, Issa A.
e52ee155-995b-4f85-aa5b-ff682978769d
Maret, Wolfgang
41845264-4c6c-4841-ae1e-a8b843c34ba4
Bury, Nic R.
696daba0-5cc9-444c-be9a-c678808712c6
Hogstrand, Christer
157377cc-b2e9-4931-8a88-0b8764362ee5
Muraina, Issa A., Maret, Wolfgang, Bury, Nic R. and Hogstrand, Christer
(2020)
Hatching gland development and hatching in zebrafish embryos: a role for zinc and its transporters Zip10 and Znt1a.
Biochemical and Biophysical Research Communications, 528 (4), .
(doi:10.1016/j.bbrc.2020.05.131).
Abstract
Zinc transporters of the ZIP (Slc39, importers) and ZnT (Slc30, exporters) protein families have evolutionary conserved roles in biology. The aim of the present study was to explore the role of zinc, and zinc transporters Zip10 and Znt1a in zebrafish hatching gland development and larval hatching. In the study, knockdown of genes for Zip10 and Znt1a in zebrafish embryos was achieved using morpholino-modified oligonucleotides. A partial loss-of-function Znt1a mutant (Znt1asa17) allowed comparison with the Znt1a morphant. Free Zn2+ in embryos and apoptosis were investigated using fluorescent dyes whereas gene expression was investigated by whole-mount in situ hybridization (WISH). The results showed high levels of free Zn2+ in the hatching gland cells (HGC) along with abundant expression of zip10 and znt1a in normal embryo. Knockdown of zip10 reduced free Zn2+ in HGC, ceased their normal developmental apoptosis, and resulted in displacement and later disappearance of hatching glands and hatching enzymes he1a and catL1b, and inability to hatch. Conversely, knockdown of znt1a or the Znt1asa17 mutation accelerated hatching and coincided with high expression of hatching enzymes and free Zn2+ in the HGC. Thus, Zip10 and free Zn2+ in the HGC are required both for their development and function. This study also demonstrated the opposite functions of the two zinc transporters, ZIP10 and ZnT1 as well as shedding light on the role of Zn2+ in regulation of the human hatching enzyme homologue, ovastacin, which is activated by zinc and cleaves the zona pellucida protein, ZP2, to prevent polyspermy
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Accepted/In Press date: 18 May 2020
Published date: 1 August 2020
Identifiers
Local EPrints ID: 475597
URI: http://eprints.soton.ac.uk/id/eprint/475597
ISSN: 0006-291X
PURE UUID: fd306e72-7293-4493-b4dc-8d256d3f5df7
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Date deposited: 22 Mar 2023 17:33
Last modified: 17 Mar 2024 04:14
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Author:
Issa A. Muraina
Author:
Wolfgang Maret
Author:
Nic R. Bury
Author:
Christer Hogstrand
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