Campbell Biology (11th Edition)
Campbell Biology (11th Edition)
11th Edition
ISBN: 9780134093413
Author: Lisa A. Urry, Michael L. Cain, Steven A. Wasserman, Peter V. Minorsky, Jane B. Reece
Publisher: PEARSON
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Chapter 17.2, Problem 1CC

MAKE CONNECTIONS → In a research artide about alkaptonuria published in 1902, Garrod suggested that humans inherit two "characters" (alleles) for a particular enzyme and that both parents must contribute a faulty version for the offspring to have alkaptonuria. Today, would this disorder be called dominant or recessive? (See Concept 14.4.)

1. What is a promoter? Is it located at the upstream or downstream end of a transcription unit?

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Q1. Predict the effects (on translation of coat gene and replicase gene) of the following mutations on phage R17 coat gene and replicase gene translation and explain the logic of your answers: a. An amber mutation (premature stop codon) six codons downstream of the coat gene initiation codon. b. Mutations in the stem loop around the coat gene initiation codon that weakens the base-pairing in the stem loop. c. Mutations in the interior of the replicase gene that cause it to base-pair with the coat gene initiation codon.
Q1: In your own words, define RNA splicing. When during gene expression does it occur? Q2: What do you predict would happen if the introns were not removed from RNA before translation? Why would it be a problem if the introns were not removed? Q3: Where is the mRNA destined to go once it has been transported out of the nucleus?
Q.) A.)Search in human genome if any examples of mRNA translated from 2 different sites?and give examples? B.)aminoacyl tRNA synthetase is specialized or not ? And why?

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Campbell Biology (11th Edition)

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