Common and distinct transcriptional signatures of mammalian embryonic lethality
More about Open Access at the CrickAuthors list
John E Collins Richard J White Nicole Staudt Ian M Sealy Ian Packham Neha Wali Catherine Tudor Cecilia Mazzeo Angela Green Emma Siragher Edward Ryder Jacqueline K White Irene Papatheodoru Amy Tang Anja Füllgrabe Konstantinos Billis Stefan H Geyer Wolfgang J Weninger Antonella Galli Myriam Hemberger Derek L Stemple Elizabeth Robertson Jim Smith Timothy Mohun David J Adams Elisabeth M Busch-Nentwich Toggle all authors (26)
Abstract
The Deciphering the Mechanisms of Developmental Disorders programme has analysed the morphological and molecular phenotypes of embryonic and perinatal lethal mouse mutant lines in order to investigate the causes of embryonic lethality. Here we show that individual whole-embryo RNA-seq of 73 mouse mutant lines (>1000 transcriptomes) identifies transcriptional events underlying embryonic lethality and associates previously uncharacterised genes with specific pathways and tissues. For example, our data suggest that Hmgxb3 is involved in DNA-damage repair and cell-cycle regulation. Further, we separate embryonic delay signatures from mutant line-specific transcriptional changes by developing a baseline mRNA expression catalogue of wild-type mice during early embryogenesis (4-36 somites). Analysis of transcription outside coding sequence identifies deregulation of repetitive elements in Morc2a mutants and a gene involved in gene-specific splicing. Collectively, this work provides a large scale resource to further our understanding of early embryonic developmental disorders.
Full text links
Publisher website (DOI) 10.1038/s41467-019-10642-x
Figshare View on figshare
Europe PubMed Central 31243271
Pubmed 31243271
Keywords
Related topics
Type of publication