Essentials of Genetics - Masteringgenetic
Essentials of Genetics - Masteringgenetic
9th Edition
ISBN: 9780134143699
Author: KLUG
Publisher: PEARSON
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Chapter 11, Problem 20PDQ

The human genome contains approximately 106 copies of an Alu sequence, one of the best-studied classes of short interspersed elements (SINEs), per haploid genome. Individual Alus share a 282–nucleotide consensus sequence followed by a 3'-adenine- rich tail region (Schmid, 1998. Nucl. Acids Res. 26: 4541–4550). Given that there are approximately 3 × 109bp per human haploid genome, about how many base pairs are spaced between each Alu sequence?

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The human genome contains approximately 106 copies of an Alusequence, one of the best-studied classes of short interspersedelements (SINEs), per haploid genome. Individual Alus share a282-nucleotide consensus sequence followed by a 3'-adeninerichtail region. Given that there are approximately 3 * 109bp per human haploid genome, about how many base pairs arespaced between each Alu sequence?
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The DNA-binding domain of each CREB protein subunit recognizes the sequence 5′–TGACGTCA–3′. Due to random chance, how often would you expect this sequence to occur in the human genome, which contains approximately 3 billion base pairs? Actually, only a few doze genes are activated by the CREB protein. Does the value of a few dozen agree with the number of random occurrences expected in the human genome? If the number of random occurrences of the sequence in the human genome is much higher than a few dozen, provide at least one explanation why the CREB protein is not activating more than a few dozen gene Actually, only a few doze genes are activated by the CREB protein. Does the value of a few dozen agree with the number of random occurrences expected in the human genome? If the number of random occurrences of the sequence in the human genome is much higher than a few dozen, provide at least one explanation why the CREB protein is not activating more than a few dozen gene
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