Abstract
Abstract
PUF RNA-binding proteins are broadly conserved stem cell regulators. Nematode PUF proteins maintain germline stem cells (GSCs) and, with key partner proteins, repress differentiation mRNAs, including
gld-1
. Here we report that PUF protein FBF-2 and its partner LST-1 form a ternary complex that represses
gld-1
via a pair of adjacent FBF-2 binding elements (FBEs) in its 3’UTR. One LST-1 molecule links two FBF-2 molecules via motifs in the LST-1 intrinsically-disordered region; the
gld-1
FBE pair includes a well-established ‘canonical’ FBE and a newly-identified noncanonical FBE. Remarkably, this FBE pair drives both full RNA repression in GSCs and full RNA activation upon differentiation. Discovery of the LST-1–FBF-2 ternary complex, the
gld-1
adjacent FBEs, and their
in vivo
significance predicts an expanded regulatory repertoire of different assemblies of PUF-partner complexes in nematode germline stem cells. It also suggests analogous PUF controls may await discovery in other biological contexts and organisms.
Publisher
Cold Spring Harbor Laboratory