On theindependent irritabilityof goldfish eggs and embryos – a living communication on the rhythmic yolk contractions in goldfish

Author:

Sanchez Paul Gerald LayagueORCID,Wang Chen-YiORCID,Li Ing-JiaORCID,Ota Kinya G.ORCID

Abstract

Rhythms play an important role in the precise spatiotemporal regulation of biological processes during development and patterning of embryos. We here investigate the rhythmic contractions of the yolk during early development of the goldfishCarassius auratus. We quantify these contractions and record robust and persistent rhythmic yolk movements that are not seen in closely-related species (carp and zebrafish). We report that yolk contractions are an intrinsic emergent property of the egg, i.e. goldfish eggs are independently irritable / excitable. These contractions do not require sperm entry / fertilization nor cell division, and they notably emerge at a precise time — suggesting that goldfish eggs are able to measure elapsed time from what we infer to be egg activation. As the yolk itself is known to confer critical cues for early dorsoventral (DV) patterning of teleost embryos, we hypothesize that its contractions in goldfish may influence the patterning process of this species. Indeed, we find that embryos in conditions that result in ventralized phenotypes (i.e. goldfish embryos acutely treated with microtubule-depolymerizing drug nocodazole and embryos of the twin-tail goldfish strainOranda) display altered yolk contraction dynamics (i.e. faster and/or stronger contractions). We aim to uncover whether the yolk contractions happening during early development of domesticated goldfish are the licensing process which explain the variety of novel DV patterning phenotypes naturally-observed in this species (e.g. twin-tail and dorsal-finless strains) and which are instead not found among closely-related species (e.g. carp) whose yolks do not contract.This manuscript is here published as a living communication (as described in Gnaiger (2021)). The authors intend to share findings when they are available, encourage feedback and discussion, and invite knowledge exchange and collaboration.

Publisher

Cold Spring Harbor Laboratory

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3