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Identification and Characterization of acis-Regulatory Element for Zygotic Gene Expression inChlamydomonas reinhardtii
Author(s) -
Takashi Hamaji,
David Lopez,
Matteo Pellegrini,
James Umen
Publication year - 2016
Publication title -
g3 genes genomes genetics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.468
H-Index - 66
ISSN - 2160-1836
DOI - 10.1534/g3.116.029181
Subject(s) - chlamydomonas reinhardtii , biology , zygote , maternal to zygotic transition , gene , genetics , promoter , transcription factor , reporter gene , chlamydomonas , transcription (linguistics) , regulation of gene expression , gene expression , response element , microbiology and biotechnology , embryogenesis , mutant , linguistics , philosophy
Upon fertilization Chlamydomonas reinhardtii zygotes undergo a program of differentiation into a diploid zygospore that is accompanied by transcription of hundreds of zygote-specific genes. We identified a distinct sequence motif we term a zygotic response element (ZYRE) that is highly enriched in promoter regions of C reinhardtii early zygotic genes. A luciferase reporter assay was used to show that native ZYRE motifs within the promoter of zygotic gene ZYS3 or intron of zygotic gene DMT4 are necessary for zygotic induction. A synthetic luciferase reporter with a minimal promoter was used to show that ZYRE motifs introduced upstream are sufficient to confer zygotic upregulation, and that ZYRE-controlled zygotic transcription is dependent on the homeodomain transcription factor GSP1. We predict that ZYRE motifs will correspond to binding sites for the homeodomain proteins GSP1-GSM1 that heterodimerize and activate zygotic gene expression in early zygotes.

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