Myc promotes polyploidy in murine trophoblast cells and suppresses senescence

Author:

Singh Vijay Pratap1,Hassan Huzaifa1,Deng Fengyan1,Tsuchiya Dai1,McKinney Sean1,Ferro Kevin1,Gerton Jennifer L.12ORCID

Affiliation:

1. Stowers Institute for Medical Research 1 , Kansas City, MO 64110 , USA

2. University of Kansas Medical Center 2 Department of Biochemistry and Molecular Biology , , Kansas City, KS 66160 , USA

Abstract

ABSTRACT The placenta is essential for reproductive success. The murine placenta includes polyploid giant cells that are crucial for its function. Polyploidy occurs broadly in nature but its regulators and significance in the placenta are unknown. We have discovered that many murine placental cell types are polyploid and have identified factors that license polyploidy using single-cell RNA sequencing. Myc is a key regulator of polyploidy and placental development, and is required for multiple rounds of DNA replication, likely via endocycles, in trophoblast giant cells. Furthermore, MYC supports the expression of DNA replication and nucleotide biosynthesis genes along with ribosomal RNA. Increased DNA damage and senescence occur in trophoblast giant cells without Myc, accompanied by senescence in the neighboring maternal decidua. These data reveal Myc is essential for polyploidy to support normal placental development, thereby preventing premature senescence. Our study, combined with available literature, suggests that Myc is an evolutionarily conserved regulator of polyploidy.

Funder

Stowers Institute for Medical Research

Publisher

The Company of Biologists

Subject

Developmental Biology,Molecular Biology

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