A cargo model of yolk syncytial nuclear migration during zebrafish epiboly

被引:11
作者
Fei, Zhonghui [1 ]
Bae, Koeun [1 ]
Parent, Serge E. [1 ]
Wan, Haoyu [1 ]
Goodwin, Katharine [2 ,4 ]
Theisen, Ulrike [3 ]
Tanentzapf, Guy [2 ]
Bruce, Ashley E. E. [1 ]
机构
[1] Univ Toronto, Dept Cell & Syst Biol, Toronto, ON M5S 3G5, Canada
[2] Life Sci Inst, Dept Cellular & Physiol Sci, Vancouver Campus,2350 Hlth Sci Mall, Vancouver, BC V6T 1Z3, Canada
[3] TU Braunschweig, Cellular & Mol Neurobiol, Zool Inst, Spielmannstr 7, D-38106 Braunschweig, Germany
[4] Princeton Univ, Dept Chem & Biol Engn, 303 Hoyt Lab,William St, Princeton, NJ 08544 USA
来源
DEVELOPMENT | 2019年 / 146卷 / 01期
基金
加拿大自然科学与工程研究理事会;
关键词
Zebrafish; Epiboly; Yolk syncytial layer; Yolk syncytial nuclei; Microtubule; LINC complex; ANTERIOR NEUROECTODERM; MICROTUBULE GROWTH; LAYER; CELL; KINESIN-1; ORGANIZER; MECHANISM; ENDODERM; PROTEINS; MESODERM;
D O I
10.1242/dev.169664
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
In teleost fish, the multinucleate yolk syncytial layer functions as an extra-embryonic signaling center to pattern mesendoderm, coordinate morphogenesis and supply nutrients to the embryo. External yolk syncytial nuclei (e-YSN) undergo microtubule-dependent movements that distribute the nuclei over the large yolkmass. Howe-YSN migration proceeds, and the role of the yolk microtubules, is not understood, but it is proposed that e-YSN are pulled vegetally as the microtubule network shortens from the vegetal pole. Live imaging revealed that nuclei migrate along microtubules, consistent with a cargo model in which e-YSN are moved down the microtubules by direct association with motor proteins. We found that blocking the plus-end directed microtubule motor kinesin significantly attenuated yolk nuclear movement. Blocking the outer nuclear membrane LINC complex protein Syne2a also slowed e-YSN movement. We propose that e-YSN movement is mediated by the LINC complex, which functions as the adaptor between yolk nuclei and motor proteins. Our work provides new insights into the role of microtubules in morphogenesis of an extra-embryonic tissue and further contributes to the understanding of nuclear migration mechanisms during development.
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页数:10
相关论文
共 78 条
[1]   Rearranging gastrulation in the name of yolk:: evolution of gastrulation in yolk-rich amniote eggs [J].
Arendt, D ;
Nübler-Jung, K .
MECHANISMS OF DEVELOPMENT, 1999, 81 (1-2) :3-22
[2]   A Transgenic Zebrafish for Monitoring In Vivo Microtubule Structures [J].
Asakawa, Kazuhide ;
Kawakami, Koichi .
DEVELOPMENTAL DYNAMICS, 2010, 239 (10) :2695-2699
[3]  
Bachop W.E, 1974, P345
[4]   Forces Driving Epithelial Spreading in Zebrafish Gastrulation [J].
Behrndt, Martin ;
Salbreux, Guillaume ;
Campinho, Pedro ;
Hauschild, Robert ;
Oswald, Felix ;
Roensch, Julia ;
Grill, Stephan W. ;
Heisenberg, Carl-Philipp .
SCIENCE, 2012, 338 (6104) :257-260
[5]   Nuclear migration events throughout development [J].
Bone, Courtney R. ;
Starr, Daniel A. .
JOURNAL OF CELL SCIENCE, 2016, 129 (10) :1951-1961
[6]   The maternally expressed zebrafish T-box gene eomesodermin regulates organizer formation [J].
Bruce, AEE ;
Howley, C ;
Zhou, Y ;
Vickers, SL ;
Silver, LM ;
King, ML ;
Ho, RK .
DEVELOPMENT, 2003, 130 (22) :5503-5517
[7]   Nuclear movement during myotube formation is microtubule and dynein dependent and is regulated by Cdc42, Par6 and Par3 [J].
Cadot, Bruno ;
Gache, Vincent ;
Vasyutina, Elena ;
Falcone, Sestina ;
Birchmeier, Carmen ;
Gomes, Edgar R. .
EMBO REPORTS, 2012, 13 (08) :741-749
[8]   Kinesin-1 interacts with Bucky ball to form germ cells and is required to pattern the zebrafish body axis [J].
Campbell, Philip D. ;
Heim, Amanda E. ;
Smith, Mordechai Z. ;
Marlow, Florence L. .
DEVELOPMENT, 2015, 142 (17) :2996-+
[9]   Temporal and tissue specific gene expression patterns of the zebrafish kinesin-1 heavy chain family, kif5s, during development [J].
Campbell, Philip D. ;
Marlow, Florence L. .
GENE EXPRESSION PATTERNS, 2013, 13 (07) :271-279
[10]   The yolk syncytial layer in early, zebrafish development [J].
Carvalho, Lara ;
Heisenberg, Carl-Philipp .
TRENDS IN CELL BIOLOGY, 2010, 20 (10) :586-592