Extended Data Fig. 4: Culturing, whole genome sequencing, and RNA–seq of Flagellimonas taeanensis strains that encode dCas12f-σE systems. | Nature

Extended Data Fig. 4: Culturing, whole genome sequencing, and RNA–seq of Flagellimonas taeanensis strains that encode dCas12f-σE systems.

From: Exapted CRISPR–Cas12f homologues drive RNA-guided transcription

Extended Data Fig. 4: Culturing, whole genome sequencing, and RNA–seq of Flagellimonas taeanensis strains that encode dCas12f-σE systems.The alternative text for this image may have been generated using AI.

a, Summary table of strain information and culturing conditions for five F. taeanensis (Fta) strains and one Mucilaginibacter rigui strain, which were acquired because of the likely presence of rpoE-dcas12f loci. The number of loci identified after whole-genome sequencing (WGS) is highlighted. b, BioCircos plots of the six strains in a after WGS analysis, with the positions of rpoE-dcas12f loci highlighted in red. Information regarding the internal strain ID, total genome size, GC content; contigs are denoted in cases where genome assembly was incomplete. c, Genomic neighbourhoods of rpoE-dcas12f loci in the indicated strains from a. Genes encoding HTH (hth), σE (rpoE) and dCas12f (dcas12f) are shown in yellow, blue, and red, respectively; gRNAs and hth-associated ncRNAs are annotated in orange and magenta, respectively. d, Magnified RNA–seq coverage plots from Fta strain sSL4759 for two distinct loci, highlighting the abundance of reads corresponding to hth-associated ncRNAs at both rpoE-dcas12f locus 1 (left) and the presumed susC target site of dCas12f-associated gRNAs (right). The top panels show a 2-kbp window; the bottom panels zoom in on the ncRNA sequence. Coverage is shown as counts per million (CPM).

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