For Cas9 sites with compatible PAMs, what directs sequence-specific targeting?
What can become a spacer in a bacterial CRISPR array?
A stored spacer must supply RNA through transcription before its sequence can guide Cas9 defence.
Circle one: True False
End joining repairs a Cas9 break without copying a donor. Which description fits its possible outcomes?
What normally helps spare the stored spacer in a native Cas9 system?
A target base is A. A matching donor has G at that position. Which outcome could homology-directed repair using this donor produce, and how?
Every new compatible DNA target requires a newly designed Cas9 protein, even when the guide can be changed.
Circle one: True False
A guide has a close DNA lookalike elsewhere beside a compatible PAM. What should researchers do about that site?