Long non-coding RNA ANRIL is required for the PRC2 recruitment to and silencing of p15INK4B tumor suppressor gene

Y Kotake, T Nakagawa, K Kitagawa, S Suzuki, N Liu… - Oncogene, 2011 - nature.com
Y Kotake, T Nakagawa, K Kitagawa, S Suzuki, N Liu, M Kitagawa, Y Xiong
Oncogene, 2011nature.com
A 42 kb region on human chromosome 9p21 encodes for three distinct tumor suppressors,
p16 INK4A, p14 ARF and p15 INK4B, and is altered in an estimated 30–40% of human
tumors. The expression of the INK4A-ARF-INK4B gene cluster is silenced by polycomb
during normal cell growth and is activated by oncogenic insults and during aging. How the
polycomb is recruited to repress this gene cluster is unclear. Here, we show that expression
of oncogenic Ras, which stimulates the expression of p15 INK4B and p16 INK4A, but not …
Abstract
A 42 kb region on human chromosome 9p21 encodes for three distinct tumor suppressors, p16 INK4A, p14 ARF and p15 INK4B, and is altered in an estimated 30–40% of human tumors. The expression of the INK4A-ARF-INK4B gene cluster is silenced by polycomb during normal cell growth and is activated by oncogenic insults and during aging. How the polycomb is recruited to repress this gene cluster is unclear. Here, we show that expression of oncogenic Ras, which stimulates the expression of p15 INK4B and p16 INK4A, but not p14 ARF, inhibits the expression of ANRIL (antisense non-coding RNA in the I NK4 locus), a 3.8 kb-long non-coding RNA expressed in the opposite direction from INK4A-ARF-INK4B. We show that the p15 INK4B locus is bound by SUZ12, a component of polycomb repression complex 2 (PRC2), and is H3K27-trimethylated. Notably, depletion of ANRIL disrupts the SUZ12 binding to the p15 INK4B locus, increases the expression of p15 INK4B, but not p16 INK4A or p14 ARF, and inhibits cellular proliferation. Finally, RNA immunoprecipitation demonstrates that ANRIL binds to SUZ12 in vivo. Collectively, these results suggest a model in which ANRIL binds to and recruits PRC2 to repress the expression of p15 INK4B locus.
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