GRE Subject Test: Biochemistry, Cell, and Molecular Biology : Help with Transposable and Repeated Elements
Study concepts, example questions & explanations for GRE Subject Test: Biochemistry, Cell, and Molecular Biology
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Example Questions
Example Question #1 : Help With Transposable And Repeated Elements
Which of the following is not true about transposable elements?
Transposable elements are primarily considered non-coding DNA
Transposable elements often move around the genome
Transposable elements can cause disease
Transposable elements are only found in eukaryotes
Transposable elements are only found in eukaryotes
Transposable elements are portions of the DNA that are free to move around the genome and are generally considered non-coding DNA. This can be potentially dangerous, however. Transposable elements can insert themselves in the coding regions of genes, thus making them non-functional. This can lead to disease. Both eukaryotic and prokaryotic genomes contain transposable elements.
Example Question #4 : Genomics
Transposable elements, or transposons, are separated into two classes. Which of these categories of life have class I transposons in their genomes?
I. Bacteria
II. Yeast
III. Eukaryotes
III only
I, II, and III
None of these
I and II
II and III
II and III
Class I transposable elements are RNA-mediated elements of a single evolutionary origin, and are found in yeast, which only have class I elements, and in eukaryotes, which have both class I and class II elements. Bacteria only have class II elements, and hence are not included in the correct answer to this question.
Example Question #5 : Genomics
What differentiates a LTR retrotransposon and a retrovirus?
LTR retrotransposons cannot move between organisms
Retroviruses do not insert DNA into their host
Retroviruses are the only ones present in eukaryotes
None of these are correct
Retroviruses encode an envelope protein
Retroviruses encode an envelope protein
The only difference between most LTR retrotransposons and retroviruses are that retroviruses can encode an envelope protein. Phylogenetic analyses have shown that retrotransposons and retroviruses are extremely closely related, and may be direct ancestors of one another.
Example Question #6 : Genomics
The hybrid dysgenesis phenomenon was observed in Drosophila flies. It was determined that this was caused by a transposon no longer under control in wild type - lab strain crosses. What are transposons commonly controlled by in their hosts?
Other types of transposons
None of these
RNAi and piRNAs
A transposase inhibitor
The immune system
RNAi and piRNAs
Movement of transposons is very commonly controlled by RNA interference. The RNAi system cuts up problematic RNAs, and uses these small pieces to target transposons for destruction.
Example Question #7 : Genomics
How do transposons rapidly propogate through and between species?
Horizontal transfer
Vertical transfer
Bacterial infections
Transposons cannot move between species
None of these are correct
Horizontal transfer
It is hypothesized that transposons can rapidly move through populations and species by horizontal transfer, most likely through viruses.
Example Question #1 : Help With Transposable And Repeated Elements
Barbara McClintock initially discovered transposons in her work on corn at Cold Spring Harbor Lab, which she called the Ac / Ds system. What were dissociators (Ds)?
A transposon that suppresses another transposon
None of these are correct
Transposons that are mobile and insert all over the genome
Genes that are interrupted by a transposon
Defective transposons that served as sites of chromosome breakage
Defective transposons that served as sites of chromosome breakage
Barbara McClintock named the transposons that are defective, and serve as sites of chromosomal breakage where other transposons insert (the associator, Ac) the dissociators. These were likely transposons that lacked the transposase that catalyzes their movement.
Example Question #2 : Help With Transposable And Repeated Elements
Transposable elements can be significant factors in causing newly resistant bacterial strains. How do transposons cause resistance to develop?
A composite of two transposons and a gene insert into the bacterial genome
A transposon modifies a bacterial resistance plasmid
Transposons are not actually involved in creating resistance
Transposons change gene expression levels
An individual transposon incorporates into the genome and is adapted
A composite of two transposons and a gene insert into the bacterial genome
Two transposons flanking an antibiotic resistance gene can easily move between bacteria and confer new resistance. A mix of transposons and new genes such as this is called a composite transposon. Recall that bacteria exchange genetic information via conjugation, transduction, and transformation.
Example Question #3 : Help With Transposable And Repeated Elements
What makes an LTR retrotransposon unique among other transposons?
LTR retrotransposons are not present in eukaryotes like humans
The transposon is bound by repeats that contain a series of proteins
The LTR regions allows insertion of the transposon anywhere in the genome, versus other restricted transposons
None of these are correct
LTR retrotransposons are derived from short RNAs
The transposon is bound by repeats that contain a series of proteins
LTR stands for Long Terminal Repeats, which are 250-500 base pair repeats located on the ends of a transposon. These repeats encode a series of proteins, most significantly transposase. These are very likely to be early evolutionarily stages of retroviruses.
Example Question #4 : Help With Transposable And Repeated Elements
How do non-LTR retrotransposons insert into the genome?
The transposon carries an RNA polymerase promoter
The transposon uses the standard transposase insertion method
The ends of the transposon mimic ribosomal RNA gene sequences
None of these are correct
Host DNA repair functions are tricked into integrating the transposon
Host DNA repair functions are tricked into integrating the transposon
Non-LTR retrotransposons use an endonuclease that nicks thymine-rich host DNA, which eventually leads to incorporation of the transposon by host DNA repair functions. These other methods are all associated with different specializations of transposon.
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