3D environment with high sensitivity and temporal resolution. In
this respect, recently developed super-resolution microscopy tech-
niques reaching unprecedented resolution hold great promises, as
they enable highly accurate codetection of transcripts and asso-
ciated molecules or cellular structures [170, 171]. A major future
challenge will be to bridge the gap between visualization and
functional study of RNAs in living samples. Latest developments
in genome engineering techniques [172], together with the imple-
mentation of tools to remotely control RNA activity [173], make it
now possible to manipulate RNAs. Applying such methods at the
systems-level should help comprehensively explore RNA functions,
and in particular elucidate the role of newly discovered noncoding
species or the impact of RNA binding to protein activity. Impor-
tantly, this will also provide an integrative view on posttranscrip-
tional strategies that have been adopted along evolution.
Acknowledgments
Work in F.B.’s lab is supported by the ARC (grant #PJA
20141201623), the ANR (through the RNAGRIMP research
grant and the ‘Investments for the Future’ LABEX SIGNALIFE
program # ANR-11-LABX-0028-01), and the JPND (FlySMALS
grant). The authors apologize to colleagues whose relevant studies
could not be cited because of space limitations.
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