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. 2016 Nov 23;5:e19881. doi: 10.7554/eLife.19881

Figure 3. EJC proteins associate with nascent transcripts of both intron and intronless genes.

(A) Immunolocalization of GFP-LacI (red band in boxed areas) at transgene insertion site: S118 (intron plus) on the X (panel I) and of S136 (intron minus) on the 3L (III) chromosome arm. Bands were mapped at 3B for S118 (II) and 63B for S136 (IV) using a standard polytene chromosome map shown above. (B) DAPI-stained (gray) segments of the X chromosome encompassing 3B (I, II) and 3L chromosome encompassing 63B (III, IV), without (I, III) or with (II, IV) ecdysone treatment, which produces a distinct puff at the transgene insertion locus. (C) Immunolocalization of RNA Pol II Ser2 (red) and eIF4AIII (green) at 3B (I-IV and IX-XII) and 63B (V-VIII and XIII-XVI) loci in S118 (I-VIII) and S136 (IX-XVI) transgene following ecdysone treatment. As there is no insert at locus 63B in S118 (V-VIII) and at 3B in S136 (IX-XII), these are used as ecdysone-unresponsive control loci for the transgene at 63B in S136 (XIII-XVI) and for 3B in S118 (I-IV), respectively. Scale bar represents 20 µm length.

DOI: http://dx.doi.org/10.7554/eLife.19881.010

Figure 3.

Figure 3—figure supplement 1. Y14 associates with nascent transcript of both intron and intronless gene reporters.

Figure 3—figure supplement 1.

Immunolocalization of RNA Pol II Ser2 (red) and Y14 (green) at an intro-containing gene reporter (S118 construct at 3B) (I-IV and IX-XII) and intronless counterpart (S136 at 63B) (V-VIII and XIII-XVI). Both genes were induced by ecdysone treatment as described in Material and methods. As there is no insert at locus 63B in S118 (V-VIII) and at 3B in S136 (IX-XII), these are used as ecdysone-unresponsive control loci for the transgene at 63B in S136 (XIII-XVI) and for 3B in S118 (I-IV), respectively.