Biology: Life on Earth with Physiology (11th Edition)
Biology: Life on Earth with Physiology (11th Edition)
11th Edition
ISBN: 9780133923001
Author: Gerald Audesirk, Teresa Audesirk, Bruce E. Byers
Publisher: PEARSON
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Chapter 13.5, Problem 1CSC
Summary Introduction

To determine:

How can a functional chloride channel (CFTR protein) produced by CFTR alleles causes cystic fibrosis.

Introduction:

Cystic fibrosis is the recessive genetic disorder caused by defective alleles of a gene that encodes a crucially important protein called CFTR (cystic fibrosis transmembrane conductance regulator). It occurs when a person is homozygous for defective CFTR alleles. The CFTR protein is found in the pancreas, intestine, sweat glands, and in the cells lining the airways of the lungs. Mutations in the CFTR genes affect the structure and function of the protein.

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Introns in mRNA bind to tRNA at the ribosome true False
Cystic Fibrosis is a genetically heritable disease caused by the loss of the chloride channel, CFTR. Studies of this gene have found that the Gene includes 250,000bp in the DNA. Scientists found that the mRNA had 6,500 nucleotides, and the final protein had 1480 amino acids. How much of the mRNA is untranslated? How much of the RNA that is produced does not leave the nucleus? One of the mutations that results in a disease phenotype can be easily identified because the mutation results in a much longer mRNA then normal. Where would you look for this mutation? What might this mutation have affected?
Spliceosomes include all of the following EXCEPT   enzymes catalyzing acetylation of histone proteins   snRNPs   RNA-annealing proteins   ATP-dependent RNA-unwinding proteins
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Mitochondrial mutations; Author: Useful Genetics;https://www.youtube.com/watch?v=GvgXe-3RJeU;License: CC-BY