Li Lin, Walsh Ryan M, Wagh Vilas, James Marianne F, Beauchamp Roberta L, Chang Yuh-Shin, Gusella James F, Hochedlinger Konrad, Ramesh Vijaya
Center for Human Genetic Research, Massachusetts General Hospital, Boston, Massachusetts, United States of America.
Center for Regenerative Medicine, Massachusetts General Hospital, Boston, Massachusetts, United States of America.
PLoS One. 2015 Oct 7;10(10):e0140192. doi: 10.1371/journal.pone.0140192. eCollection 2015.
The multi-subunit mammalian Mediator complex acts as an integrator of transcriptional regulation by RNA Polymerase II, and has emerged as a master coordinator of development and cell fate determination. We previously identified the Mediator subunit, MED28, as a cytosolic binding partner of merlin, the Neurofibromatosis 2 (NF2) tumor suppressor, and thus MED28 is distinct in having a cytosolic role as an NF2 interacting protein as well as a nuclear role as a Mediator complex subunit. Although limited in vitro studies have been performed on MED28, its in vivo function remains unknown. Employing a knockout mouse model, we describe for the first time the requirement for Med28 in the developing mouse embryo. Med28-deficiency causes peri-implantation lethality resulting from the loss of pluripotency of the inner cell mass accompanied by reduced expression of key pluripotency transcription factors Oct4 and Nanog. Further, overexpression of Med28 in mouse embryonic fibroblasts enhances the efficiency of their reprogramming to pluripotency. Cre-mediated inactivation of Med28 in induced pluripotent stem cells shows that Med28 is required for their survival. Intriguingly, heterozygous loss of Med28 results in differentiation of induced pluripotent stem cells into extraembryonic trophectoderm and primitive endoderm lineages. Our findings document the essential role of Med28 in the developing embryo as well as in acquisition and maintenance of pluripotency during reprogramming.
多亚基哺乳动物中介体复合物作为RNA聚合酶II转录调控的整合因子,已成为发育和细胞命运决定的主要协调者。我们之前鉴定出中介体亚基MED28是神经纤维瘤病2(NF2)肿瘤抑制因子默林的胞质结合伴侣,因此MED28的独特之处在于,它作为NF2相互作用蛋白具有胞质作用,同时作为中介体复合物亚基具有核作用。尽管对MED28进行的体外研究有限,但其体内功能仍然未知。利用基因敲除小鼠模型,我们首次描述了Med28在发育中的小鼠胚胎中的需求。Med28缺陷导致植入前致死,这是由于内细胞团多能性丧失,同时关键多能性转录因子Oct4和Nanog的表达降低所致。此外,在小鼠胚胎成纤维细胞中过表达Med28可提高其重编程为多能性的效率。在诱导多能干细胞中通过Cre介导使Med28失活表明,Med28是其存活所必需的。有趣的是,Med28的杂合缺失导致诱导多能干细胞分化为胚外滋养外胚层和原始内胚层谱系。我们的研究结果证明了Med28在发育中的胚胎以及重编程过程中多能性的获得和维持中的重要作用。