In Apis mellifera (honeybees), female larvae are genetically identical at hatching, yet develop into morphologically and behaviorally divergent castes—either reproductive queens or sterile workers. For decades, researchers attributed this phenotypic divergence solely to nutritional differences, specifically the presence of royal jelly in the larval diet. However, recent molecular investigations have revealed that epigenetic modifications mediate this developmental bifurcation. In particular, the enzyme DNA methyltransferase 3 (DNMT3) adds methyl groups to cytosine bases in larval DNA, silencing specific genetic programs required for queen development. When researchers experimentally silenced the gene encoding DNMT3 in newly hatched worker-destined larvae fed a standard worker diet, a substantial proportion developed queen-like physiological traits, including functional ovaries and queen-specific mandibular gland secretions. Conversely, larvae provided royal jelly naturally exhibit suppressed DNMT3 activity, permitting the expression of the queen phenotype. These findings demonstrate that worker sterility is actively enforced by DNA methylation rather than being a default physiological state.
Based on the passage, which of the following statements are logically supported? (Select all that apply.)
- The physiological development of worker honeybees involves active epigenetic suppression of genetic pathways that would otherwise produce queen characteristics.Cevap
- Artificially suppressing the expression of the DNMT3 gene in larvae on a worker diet can yield anatomical traits that normally require a royal jelly diet to emerge.Cevap
- CRoyal jelly contains specialized biochemical compounds that directly stimulate the transcription of worker-suppression genes.
- DNewly hatched female honeybee larvae already possess distinct underlying DNA sequences corresponding to their eventual caste outcomes.
- EExperimental inhibition of DNMT3 in honeybee larvae produces reproductive queens across all social insect species.