In a lysosomal storage disease, newly synthesized lysosome hydrolases are secreted from the cells rather than being delivered to the lysosomes. What is one possible mechanism for this result?
The cis-Golgi network lacks a proton gradient
The ER is unable to produce lysosomal vesicles
Lysosomal enzymes are not phosphorylated in the rER
Mannose is not phosphorylated in the cis-Golgi network
All the hydrolase genes are mutated, resulting in synthesis by ribosomes free in the cytoplasm rather than on the endoplasmic reticulum membrane
Mannose is not phosphorylated in the cis-Golgi network