TLS Online TPP Program

#Question id: 8689


Which of the following statements best describes the rationale for applying the principle of maximum parsimony in constructing phylogenetic trees?

#Unit 9. Diversity of Life Forms
  1. Parsimony allows the researcher to "root" the tree.
  2. Similarity due to common ancestry should be more common than similarity due to convergent evolution.
  3. The molecular clock validates the principle of parsimony.
  4. The outgroup roots the tree, allowing the principle of parsimony to be applied.
More Questions
TLS Online TPP Program

#Question id: 4254

#Unit 3. Fundamental Processes

Which of the following statements is the most current description of a gene?

TLS Online TPP Program

#Question id: 4255

#Unit 3. Fundamental Processes

How might a single base substitution in the sequence of a gene affect the amino acid sequence of a protein encoded by the gene?

TLS Online TPP Program

#Question id: 4256

#Unit 2. Cellular Organization

With respect to CpG islands in our genomic DNA, which, if any, of the following descriptions do not apply?

1) frequently occurring (there are about 30,000 in the human genome).

2) long DNA sequences (typically from 10 kb to 100 kb in length).

3) low CG dinucleotide frequency.

4) frequently associated with transcriptional start sites.

TLS Online TPP Program

#Question id: 4257

#Unit 3. Fundamental Processes

An original section of DNA has the base sequence AGCGTTACCGT. A mutation in this DNA strand results in the base sequence AGGCGTTACCGT. What type of mutation does this change represent?

TLS Online TPP Program

#Question id: 4258

#Unit 3. Fundamental Processes

A single base substitution mutation is likely to have a less deleterious effect when the base change exhibits which of the following results?

TLS Online TPP Program

#Question id: 4259

#Unit 3. Fundamental Processes

Rank the following one-base point mutations with respect to their likelihood of affecting the structure of the corresponding polypeptide (from most likely to least likely).

1. insertion mutation deep within an intron

2. substitution mutation at the third position of a codon in an exon

3. substitution mutation at the second position of a codon in an exon

4. deletion mutation within the first exon of the gene