Chapter 3, Problem 10RQ

Which of the following statements is correct? a. Ribosomes are only found in bacteria and archaea. b. Some animal cells are prokaryotic c. Only eukaryotic cells have mitochondria d. The plasma membrane is the outermost boundary of all cells. e. Some cell membranes do not consists of lipids.

Match each organelle with its correct function.

Assign a function(s) to the following cellular structures: a. plasma membrane b. mitochondrion c. nucleus d. ribosome

Organelles and Cystic Fibrosis A plasma membrane transport protein called CFTR moves chloride ions out of cells lining cavities and ducts of the lungs, liver, pancreas, intestines, and reproductive system. Water that follows the ions creates a thin film that allows mucus to slide easily through these structures. People with cystic fibrosis (CF) have too few copies of the CFTR protein in the plasma membranes of their cells. Not enough chloride ions leave the cells, and so not enough water leaves them either. The result is thick, dry mucus that clogs the airways to the lungs and other passages. Symptoms include difficulty breathing and chronic lung infections. In 2000, researchers tracked the cellular location of the CFTR protein as it was being produced in cells from people with CF (Figure 3.13). Figure 3.13 Cellular location of the CFTR protein. Graph compares the amounts of CFTR protein found in endoplasmic reticulum, vesicles travel in g from ER to Golgi, and Golgi bodies in CF cells and normal cells. Which organelle contains the least amount of CFTR protein in normal cells? In CF cells?

Organelles and Cystic Fibrosis A plasma membrane transport protein called CFTR moves chloride ions out of cells lining cavities and ducts of the lungs, liver, pancreas, intestines, and reproductive system. Water that follows the ions creates a thin film that allows mucus to slide easily through these structures. People with cystic fibrosis (CF) have too few copies of the CFTR protein in the plasma membranes of their cells. Not enough chloride ions leave the cells, and so not enough water leaves them either. The result is thick, dry mucus that clogs the airways to the lungs and other passages. Symptoms include difficulty breathing and chronic lung infections. In 2000, researchers tracked the cellular location of the CFTR protein as it was being produced in cells from people with CF (Figure 3.13). Figure 3.13 Cellular location of the CFTR protein. Graph compares the amounts of CFTR protein found in endoplasmic reticulum, vesicles traveling from ER to Golgi, and Golgi bodies in CF cells and normal cells. In which organelle is the amount of CFTR protein most similar in both types of cells?

The main function of the endomembrane system is _______ . a. building and modifying proteins and lipids b. isolating DNA from toxic substances c. secreting extracellular matrix onto the cell surface d. producing ATP by aerobic respiration

What controls the passage of molecules into and out of the nucleus? a. endoplasmic reticulum, an extension of the nucleus b. nuclear pores, which consists of membrane proteins c. nucleoli, in which ribosome subunits are made d. dynamically assembled microtubules e. tight junctions

Enzymes contained in __________ break down worn-out organelles, bacteria, and other particles. a. lysosomes b. mitochondria c. endoplasmic reticulum d. peroxisomes

Why is cell furrowing important in cell division? If cytokinesis did not occur, what would be the end result?