SALL4 controls cell fate in response to DNA base composition

Mammalian genomes contain long domains with distinct average compositions of A/T versus G/C base pairs. In a screen for proteins that might interpret base composition by binding to AT-rich motifs, we identified the stem cell factor SALL4, which contains multiple zinc fingers. Mutation of the domain responsible for AT binding drastically reduced SALL4 genome occupancy and prematurely upregulated genes in proportion to their AT content. Inactivation of this single AT-binding zinc-finger cluster mimicked defects seen in Sall4 null cells, including precocious differentiation of embryonic stem cells (ESCs) and embryonic lethality in mice. In contrast, deletion of two other zinc-finger clusters was phenotypically neutral. Our data indicate that loss of pluripotency is triggered by downregulation of SALL4, leading to de-repression of a set of AT-rich genes that promotes neuronal differentiation. We conclude that base composition is not merely a passive byproduct of genome evolution and constitutes a signal that aids control of cell fate.

Automated summary

This study identified SALL4 as a protein that interprets base composition by binding to AT-rich motifs, affecting genome occupancy and genes regulation. Loss of pluripotency is triggered by downregulation of SALL4, leading to de-repression of a set of AT-rich genes promoting neuronal differentiation. Deletion of two other zinc-finger clusters had no phenotypic effect, indicating the importance of SALL4 in controlling cell fate.