| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5534211 | Molecular and Cellular Endocrinology | 2017 | 7 Pages |
•ChIP-Seq and microarray show SRC-1 regulated genes not dependent on E2 signaling.•SRC-1 regulates genes critical in osteoblast differentiation independent of ERα.•SRC-1 affects bone formation by altering how osteoblasts secrete ALPL and OCN.
Steroid receptor coactivator-1 (SRC-1), a well-studied coactivator of estrogen receptor (ER), is known to play an important and functional role in the development and maintenance of bone tissue. Previous reports suggest SRC-1 maintains bone mineral density primarily through its interaction with ER. Here we demonstrate that SRC-1 can also affect bone development independent of estrogen signaling as ovariectomized SRC-1 knockout (SRC-1 KO) mouse had decreased bone mineral density. To identify estrogen-independent SRC-1 target genes in osteoblastogenesis, we undertook an integrated analysis utilizing ChIP-Seq and mRNA microarray in transformed osteoblast-like U2OS-ERα cells. We identified critical osteoblast differentiation genes regulated by SRC-1, but not by estrogen including alkaline phosphatase and osteocalcin. Ex vivo primary culture of osteoblasts from SRC-1 wild-type and KO mice confirmed the role of SRC-1 in osteoblastogenesis, associated with altered ALPL levels. Together, these data indicate that SRC-1 can impact osteoblast function in an ER-independent manner.
