Sigma factor specificity—what does the bacterial holoenzyme recognize? During transcription initiation in bacteria, the RNA polymerase holoenzyme (core + sigma) recognizes which promoter elements?

Introduction / Context:
Promoter recognition in bacteria depends on the sigma factor, which confers sequence specificity to the RNA polymerase core enzyme. The canonical promoter contains two key hexamer elements centered near -10 and -35 relative to the transcription start site.

Given Data / Assumptions:

• Consensus sequences: -10 (Pribnow box) and -35 motifs.
• Sigma factor contacts both regions during closed and open complex formation.

Concept / Approach:
The holoenzyme binds and recognizes both elements to position polymerase correctly and to facilitate melting at -10. Variations exist across promoters and sigma factors, but the classic model involves recognition of both the -10 and -35 sites.

Step-by-Step Solution:
Identify the bacterial initiation machinery: RNA polymerase + sigma.Recall canonical promoter architecture: -35 and -10 hexamers.Select the option indicating recognition of both.

Verification / Alternative check:
Mutational analyses reducing matches to either element diminish binding/initiation; sigma factor crosslinking shows contacts at both motifs.

Why Other Options Are Wrong:

• Only one element: Oversimplifies typical promoter recognition.
• None of the above / only UP element: UP elements aid some promoters but are not universally recognized by all sigmas.

Common Pitfalls:
Assuming -10 alone defines promoter strength; spacing and -35 integrity are critical.

Final Answer:
Both the -10 element and the -35 element.