Lysosomal storage diseases:

• Hurler’s disease

• Inclusion-cell disease

TLS Online TPP Program

#Id: 8218

#Section 3: Genetics, Cellular and Molecular Biology

Sorting signal that directs lysosomal hydrolases from the TGN to the late endosome is- Mannose 6-phosphate (M6P).

TLS Online TPP Program

#Id: 8217

#Section 3: Genetics, Cellular and Molecular Biology

In selective autophagy

specific cargo is packaged into autophagosomes that tend to contain little cytosol, mediates the degradation of worn out, or unwanted, mitochondria, peroxisomes, ribosomes, and ER; used to destroy invading microbes.

TLS Online TPP Program

#Id: 8216

#Section 3: Genetics, Cellular and Molecular Biology

In nonselective autophagy, a bulk portion of cytoplasm is sequestered in autophagosomes

TLS Online TPP Program

#Id: 8215

#Section 3: Genetics, Cellular and Molecular Biology

Autophagy can be either

• Nonselective autophagy

• Selective autophagy

TLS Online TPP Program

#Id: 8213

#Section 3: Genetics, Cellular and Molecular Biology

Autophagy occurs in the following sequence of steps:

Induction by activation of mTOR complex 1

• Nucleation of autophagosome formation by ATG9

• Closure of the membrane cup to form autophagosome

• Fusion of the autophagosome with lysosomes, catalyzed by SNAREs.

• Digestion of the inner membrane and the lumenal contents of the autophagosome

TLS Online TPP Program

#Id: 8212

#Section 3: Genetics, Cellular and Molecular Biology