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. 2018 Oct 22;13(10):e0205867. doi: 10.1371/journal.pone.0205867

Fig 1. HP1b16 and HP1b 86 are null alleles.

Fig 1

A. Top—diagram showing the genomic region near the HP1b locus on the X chromosome. The P element mobilized to generate the HP1b alleles is indicated by a triangle above the genes shown in blue above the position on the X chromosome (bp). Black arrows mark the primers used to screen for deletions. Bottom—close-up of HP1b with the three deletion alleles shown below. All three deletions remove the HP1b start codon. B. RT-PCR analysis shows that full-length HP1b mRNA is transcribed in wildtype OR embryos, but not in HP1b16 or HP1b86 homozygous embryos. CG7346 and APC4 are transcribed in all samples, as is the Rpl32 positive control. RT: reverse transcriptase. C. No HP1B protein is detected in HP1b16 and HP1b86 homozygous larvae (left panel; *); Actin (right panel; **) serves as loading control.