Towards Functional Annotation of the Preimplantation Transcriptome: An RNAi Screen in Mammalian Embryos

被引:28
作者
Cui, Wei [1 ]
Dai, Xiangpeng [2 ]
Marcho, Chelsea [1 ]
Han, Zhengbin [1 ,3 ]
Zhang, Kun [4 ]
Tremblay, Kimberly D. [1 ]
Mager, Jesse [1 ]
机构
[1] Univ Massachusetts, Dept Vet & Anim Sci, Amherst, MA 01003 USA
[2] Harvard Med Sch, Beth Israel Deaconess Med Ctr, Dept Pathol, Boston, MA 02215 USA
[3] Harbin Inst Technol, Sch Life Sci & Technol, Harbin 150080, Peoples R China
[4] Zhejiang Univ, Coll Anim Sci, Inst Anim Genet & Reprod, Lab Mammalian Mol Embryol, Hangzhou 310058, Zhejiang, Peoples R China
来源
SCIENTIFIC REPORTS | 2016年 / 6卷
关键词
DOUBLE-STRANDED-RNA; CELL FATE; ZYGOTIC TRANSITION; BREAST-CANCER; MOUSE OOCYTES; DYNAMICS; REVEALS; INTERFERENCE; EXPRESSION; SPECIFICATION;
D O I
10.1038/srep37396
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
With readily available transcriptome-wide data, understanding the role of each expressed gene is an essential next step. Although RNAi technologies allow for genome-wide screens in cell culture, these approaches cannot replace strategies for discovery in the embryo. Here we present, for the first time, a knockdown screen in mouse preimplantation embryos. Early mammalian development encompasses dynamic cellular, molecular and epigenetic events that are largely conserved from mouse to man. We assayed 712 genes for requirements during preimplantation. We identified 59 genes required for successful development or outgrowth and implantation. We have characterized each phenotype and revealed cellular, molecular, and lineage specific defects following knockdown of transcript. Induced network analyses demonstrate this as a valid approach to identify networks of genes that play important roles during preimplantation. Our approach provides a robust and efficient strategy towards identification of novel phenotypes during mouse preimplantation and facilitates functional annotation of the mammalian transcriptome.
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页数:12
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