Cytoplasmic polyadenylation-mediated translational control of maternal mRNAs directs maternal-to-zygotic transition
Author(s) -
Cecilia Lanny Winata,
Maciej Łapiński,
Leszek P. Pryszcz,
Candida Vaz,
Muhammad Hisyam bin Ismail,
Srikanth Nama,
Hajira Shreen Hajan,
Serene Gek Ping Lee,
Vladimir Korzh,
Prabha Sampath,
Vivek Tanavde,
Sinnakaruppan Mathavan
Publication year - 2018
Publication title -
development
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.754
H-Index - 325
eISSN - 1477-9129
pISSN - 0950-1991
DOI - 10.1242/dev.159566
Subject(s) - maternal to zygotic transition , biology , polyadenylation , transcriptome , zebrafish , microbiology and biotechnology , chromatin , translational regulation , genetics , polysome , gene expression , regulation of gene expression , gene , messenger rna , rna , zygote , embryogenesis , translation (biology) , ribosome
In the earliest stages of animal development following fertilization, maternally deposited mRNAs direct biological processes to the point of zygotic genome activation (ZGA). These maternal mRNAs undergo cytoplasmic polyadenylation (CPA), suggesting translational control of their activation. To elucidate the biological role of CPA during embryogenesis, we performed genome-wide polysome profiling at several stages of zebrafish development. Our analysis revealed a correlation between CPA and polysome-association dynamics, demonstrating a coupling of translation to the CPA of maternal mRNAs. Pan-embryonic CPA inhibition disrupted the maternal-to-zygotic transition (MZT), causing a failure of developmental progression beyond the mid-blastula transition and changes in global gene expression that indicated a failure of ZGA and maternal mRNA clearance. Among the genes that were differentially expressed were those encoding chromatin modifiers and key transcription factors involved in ZGA, including nanog , pou5f3 and sox19b , which have distinct CPA dynamics. Our results establish the necessity of CPA for ensuring progression of the MZT. The RNA-seq data generated in this study represent a valuable zebrafish resource for the discovery of novel elements of the early embryonic transcriptome.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom