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Identification of four genes required for mammalian blastocyst formation

Published online by Cambridge University Press:  05 December 2012

Marc Maserati ,
Xiangpeng Dai ,
Melanie Walentuk  and
Jesse Mager
Marc Maserati
Affiliation:
Department of Veterinary and Animal Science, University of Amherst, MA 01003, USA.
Xiangpeng Dai
Affiliation:
Department of Pathology, Beth Israel Deaconess Medical Center, Harvard Medical School, 330 Brookline Ave, Boston, MA 02215, USA.
Melanie Walentuk
Affiliation:
Mass General Fertility Center, 55 Fruit St., Yawkey Building 10A, Boston, MA 02114, USA.
Jesse Mager*
Affiliation:
University of Massachusetts, Amherst, 661 North Pleasant Street, Amherst, MA 01003, USA.
*
All correspondence to: Jesse Mager. University of Massachusetts, Amherst, 661 North Pleasant Street, Amherst, MA 01003, USA. Tel: +1 413 545 7368. Fax: +1 413 545 6326. e-mail: [email protected]
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Summary

RNA transcription, processing and translation are fundamental molecular processes required for development, growth and cell viability. Towards the functional annotation of the genome, we are engaged in a reverse genetic screen using mammalian preimplantation embryos as a model system. Here we report the essential function of four RNA processing/splicing factors (Sf3b14, Sf3b1, Rpl7l1, and Rrp7a) and show that each of these genes is required for blastocyst formation in the mouse. As very little information is known about these genes, we characterized their normal expression and localization in mouse embryos as well as phenotypic analysis of loss of function during preimplantation development. Functional knockdown of each gene product results in normal morula development but there is failure to form a blastocoel cavity or morphologically differentiated trophectoderm. We show that zygotic genome activation does occur as well as initial lineage specification in the absence of each factor. Consistent with a role in RNA splicing, we demonstrate that the absence of Sf3b14 and Sf3b1 in 8-cell and morula-stage embryos results in a specific reduction of intron containing transcripts, but no reduction single-exon genes. Taken together, we show critical developmental and molecular requirements of Sf3b14, Sf3b1, Rpl7l1, and Rrp7a during mammalian preimplantation.

Keywords

PreimplantationRNAiRpl7l1Rrp7aSf3b1Sf3b14
Type
Research Article
Information
Zygote , Volume 22 , Issue 3 , August 2014 , pp. 331 - 339
Copyright
Copyright © Cambridge University Press 2012 

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