RNA Detection

(nextflipdebug2) #1

  1. For quantification of the number of moving mRNAs analyze
    about 30 cells. Calculation of the number of moving mRNA
    per cell is depending on the length of the analyzed hyphae
    (Fig.4c). In our case, most mRNAs can be detected simulta-
    neously with the MS2 system and by either the PP7 or theλN
    system.


4 Notes



  1. In order to adapt the system to other target mRNAs with for
    example altered expression levels or to use the system in other
    organisms it is advisable to fine tune the number of stem-loops
    to obtain optimal results. Therefore, it might be necessary to
    design the array of stem-loops de novo. In this case, we recom-
    mend using the sequence information given in Fig.4a for the
    stem-loops and separate the stem-loops by spacer sequences of
    about 40 nucleotides. The spacer sequences should vary to
    improve genetic stability and expression of the tagged mRNA
    [38]. After optimization of the sequence we strongly recom-
    mend to verify correct stem-loop folding in silico using the web
    program mFold (http://unafold.rna.albany.edu/?q¼mfold).
    The required plasmid DNA can be ordered by various compa-
    nies offering gene synthesis. If then for example an array of 16
    stem-loops is available, oligonucleotides for PCR reactions can
    be easily directed against the spacer sequences to obtain PCR
    products containing for example 6, 8, or 12 stem-loops.

  2. To construct vectors encoding a C-terminal fusion of the RBP
    fused to a fluorescent protein we recommend the use of the
    versatile Golden-Gate cloning system recently established for
    U. maydis[34]. In brief, the stop codon of the RBP of interest
    is replaced by a sequence encoding a short linker amino acid
    sequence AANAAT, which is fused to the start codon of the FP
    such as GFP. This is achieved by using the DNA sequence
    GCGGCCAACGCGGCCACC [33]. Thereby anSfiI restric-
    tion enzyme site (underlined) is introduced that can also be
    used for further standard cloning procedures, if for example the
    FP should be replaced by a different color (e.g., replace GFP
    with mCherry; [33]).

  3. Switching the nitrogen source induces the hyphal growth ofU.
    maydisdue to the expression of the responsible genes with the
    nar1promoter [39].

  4. Swaying the microscope slide ensures an appropriate distribu-
    tion of cells. It is highly recommended to let the cell suspension
    dry on the slide to increase plane orientation of hyphae.

  5. For better visualization the exposure time can be adjusted
    ranging from 100 to 250 ms.


332 Sabrina Zander et al.

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