The question is...
Based on the data presented in the passage, which statement best describes the HSP110ΔE9 allele?
The passage stated, "Researchers studying MSI in CRC cell lines and primary tumors observed that 100% of those analyzed contained deletions of 3 to 8 base pairs in the 17-thymine nucleotide microsatellite (T17) located in Intron 8 of the gene encoding heat shock protein 110 (HSP110)..." The larger deletions form "the mutant protein HSP110ΔE9. People with MSI CRC have HSP110ΔE9 transcripts in cancerous tissue only."
Later, Figure 1 shows that HSP110ΔE9 produces lower-volume tumors than HSP110WT.
These two points seem contradictory to me. The text makes it sound like HSP110ΔE9 is cancer-promoting, but the figure indicates that it's cancer-suppressing (or at least less cancer-promoting than the WT).
Is there something I'm missing?
Based on the data presented in the passage, which statement best describes the HSP110ΔE9 allele?
- A.
Cancer-promoting and dominant to HSP110WT - B.
Cancer-promoting and recessive to HSP110WT - C.
Cancer-suppressing and dominant to HSP110WT - D.
Cancer-suppressing and recessive to HSP110WT
The passage stated, "Researchers studying MSI in CRC cell lines and primary tumors observed that 100% of those analyzed contained deletions of 3 to 8 base pairs in the 17-thymine nucleotide microsatellite (T17) located in Intron 8 of the gene encoding heat shock protein 110 (HSP110)..." The larger deletions form "the mutant protein HSP110ΔE9. People with MSI CRC have HSP110ΔE9 transcripts in cancerous tissue only."
Later, Figure 1 shows that HSP110ΔE9 produces lower-volume tumors than HSP110WT.
These two points seem contradictory to me. The text makes it sound like HSP110ΔE9 is cancer-promoting, but the figure indicates that it's cancer-suppressing (or at least less cancer-promoting than the WT).
Is there something I'm missing?