RNA Detection

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  1. After finding an appropriate cell, fine-tune the focus to an
    appropriate position for observation of the target RNA.

  2. Capture images (Fig.4) and movies.


4 Notes



  1. The expression plasmids and their sequence information are
    available from the authors’ lab (http://www.chem.s.u-tokyo.
    ac.jp/~analyt/en/home_en.html).

  2. The dissociation constant of PUM-HD mutants to the recog-
    nized 8-base RNA is largely dependent on the three RNA bases
    at the 5^0 terminus [8]. When the three bases are 5^0 -UGU-3^0 ,
    the dissociation constant is reported to be nanomolar, whereas
    the three-base sequence is not UGU, the dissociation constant
    is approximately 100 nM. In case of mPUMt, the initial three-
    base sequence is UUA. The dissociation constant was 100 nM.

  3. A short incubation time after transfection of the TERRA probe
    is recommended to avoid excess expression of the probe. Given
    the irreversible reaction of EGFP reconstitution, overexpres-
    sion of the probe molecule results in accumulation of recon-
    stituted EGFP, which outnumbers TERRA and which
    generates a severe background fluorescence signal in the obser-
    vation. Therefore, the expression level of the probe is expected
    to be sufficiently small by making the incubation time after the
    transfection much shorter than described in the transfection
    reagent manufacturer’s protocols.

  4. In oblique illumination, making the light thin results in a high
    signal-to-noise ratio because background fluorescence from
    out-of-focus regions is eliminated, whereas the visible field
    area becomes small [22]. In case of our TERRA observation,
    the target RNA localizes in the nucleus. We made the


Fig. 4Images of TERRA using present methods: (A) TERRA labeled with the present probe, (B) iRFP-TRF1 that
represent telomeres, (C) hnRNPA1-SNAP-TMR, and (D) merge image


Spatiotemporal Imaging of Single Telomeric-Repeat Containing RNA 345
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