Chapter 18 Part II Flashcards
Gene expression can be fine-tuned
- after transcription that enables the cell to rapidly respond to specific cellular needs
- 2 post-transcription ways and 1 post-translation
1) Alternative RNA splicing
2) mRNA degradation or destruction
3) Translation initiation and post-translation
1) Alternative RNA splicing
- different mRNA molecules are produced from the same primary transcript
- create RNA variation or different lengths
2) mRNA degradation or destruction
in the cytoplasm is an important factor in determining the protein synthesis in a cell
- degrade
3) Translation initiation and post-translation
of various types of protein processing are also subject to control
Protein processing after translation
including cleavage and the addition of chemical groups, are subject to control
Ubiquitin
will tag proteins and target them for destruction
Proteasomes
giant protein complexes that bind protein molecules and degrade them
Cancer
may result from genetic changes that affect normal genes for cell cycle control and gene regulation systems
i.e. Ras, ERK, ELK-1, p53
Oncogene
cancer-causing genes
Proto-oncogenes
normal cellular genes that code for proteins that stimulate normal growth and division
i.e. RAS, ERK, ELK-1
Tumor-suppressor genes
encode proteins that inhibit abnormal cell division
i.e. p53
DNA change of a proto-oncogene
that makes a proto-oncogene excessively active converts it to an oncogene, which may promote excessive cell division and cancer
Conversion of photo-oncogene to an oncogene
can lead to abnormal stimulation of the cell cycle by
1) movement of DNA
2) Amplification
3) Point mutations
1) Movement of DNA within the genome
if it ends up near an active promoter, transcription may increase
2) Amplification of a proto-oncogene
increases the number of copies of the gene