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#DNA modification

2 public questions tagged with this topic.

Which base does DMS specifically modify in Maxam-Gilbert method?

Maxam-Gilbert sequencing is a chemical method where base-specific reagents modify nucleotides before piperidine cleavage. Dimethyl sulfate, DMS, methylates guanine at the N7 position, making the glycosidic bond labile and susceptible to breakage. Upon hot piperidine treatment, the strand cleaves at methylated guanines, producing fragments terminating at G positions specifically. Under different conditions DMS also methylates adenine, but classical G reaction uses low temperature to favor guanine selectivity. Thymine and cytosine are targeted by hydrazine instead, adenine by formic acid chemistry.

Ref: NCERT Biology Class XII Principles on Klenow fill-in labeling, Lehninger Chapter 9 DNA cloning techniques, and Molecular Cloning by Sambrook Chapter 10 documenting end-labeling of cohesive termini.

DNA

Which modification is commonly found in bacterial DNA?

N6-Methyladenosine is the correct answer as it accurately identifies the biological location, composition, or distribution described in this question. In Nucleic Acid, the spatial organization and localization of molecules are critical to their function. N6-Methyladenosine is specifically associated with the structure or compartment mentioned because of its unique biochemical properties and physiological role. The other options (5-Methylcytidine, Pseudouridine, and 7-Methylguanine) are primarily associated with different cellular compartments, tissues, or structural contexts.

Ref: Campbell Biology, Urry et al., 12th Ed.