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. Author manuscript; available in PMC: 2020 Jun 6.
Published in final edited form as: Mol Cell. 2019 May 7;74(5):982–995.e6. doi: 10.1016/j.molcel.2019.04.006

Figure 5. Armi ATPase activity enables correct substrate selection.

Figure 5.

(A) Scatter plot of the abundance of transposon- or gene-mapping 5′ monophosphorylated RNA >150 nt co-immunoprecipitated with transgenic FLAG-Myc-ArmiK729A, FLAG-Myc-ArmiDE862,863AA, FLAG-Myc-ArmiE863Q versus FLAG-Myc-Armi.

(B) Immunofluorescence detection using anti-FLAG antibody of transgenic FLAG-Myc-Armi, FLAG-Myc-ArmiK729A, FLAG-Myc-ArmiDE862,863AA or FLAG-Myc-ArmiE863Q in armi mutant germ cells from stage 3 egg chambers.

See also Figure S6.