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The U.S. Department of Justice has established a database that catalogs \(P C R\) amplification products from short tandem repeats of the \(Y\) (Y-SIRs) chromosome in humans. The database contains polymorphisms of five U.S. ethnic groups (African Americans, European Americans, Hispanics, Native Americans, and Asian Americans) as well as worldwide population (a) Given that STRs are repeats of varying lengths, for example \((\mathrm{TCTG})_{9-17}\) or \((\mathrm{TAT})_{6-14}\) explain how PCR could reveal differences (polymorphisms) among individuals. How could the Department of Justice make use of those differences? (b) \(Y-S T R s\) from the nonrecombining region of the \(Y\) chromosome (NRY) have special relevance for forensic purposes. Why? (c) What would be the value of knowing the ethnic population differences for \(Y\) -STR polymorphisms? (d) For forensic applications, the probability of a "match" for a crime scene DNA sample and a suspect's DNA often culminates in a guilty or innocent verdict. How is a "match" determined, and what are the uses and limitations of such probabilities?

Short Answer

Expert verified
Answer: Some limitations of using DNA matches in forensic applications include the possibility of false matches due to laboratory errors, cross-contamination, or the presence of identical twins. Additionally, the absence of a DNA match does not necessarily mean the suspect is innocent; it could indicate that evidence was lost or not found. It is crucial to consider the context and corroborate DNA evidence with other types of evidence to ensure a reliable verdict.

Step by step solution

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a) Understanding Polymerase Chain Reaction (PCR) and its application

PCR is a technique used to amplify a specific DNA sequence, producing millions of copies. It can reveal differences (polymorphisms) among individuals by amplifying the short tandem repeats (STRs) in their DNA. These polymorphisms can be observed by analyzing the lengths of amplified DNA fragments. The Department of Justice can use these differences to distinguish between individuals and help in identifying potential suspects in criminal cases by comparing DNA samples found at crime scenes with those stored in the database.
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b) Relevance of Y-STRs from the NRY region for forensic purposes

Y-STRs are present in the nonrecombining region of the Y chromosome (NRY), which means that they do not undergo recombination during the formation of sperm cells. This makes them particularly relevant for forensic purposes because Y-STR patterns are passed from father to son with minimal alterations. Consequently, Y-STRs can be used in cases where biological evidence contains exclusively male DNA, for example, in sexual assault cases, as well as in paternity testing and tracing male lineage in genealogical studies.
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c) The value of knowing ethnic population differences for Y-STR polymorphisms

Knowing the ethnic population differences for Y-STR polymorphisms can help increase the accuracy and relevance of forensic DNA analysis. Different ethnic groups may have distinctive Y-STR patterns, which can aid in narrowing down the pool of potential suspects, providing valuable context in investigations. Additionally, understanding ethnic distribution of Y-STR polymorphisms can facilitate the improvement of the statistical analysis models used in calculating the probability of a DNA match, further enhancing the reliability of forensic evidence.
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d) Determining a DNA "match" and its uses, limitations

A DNA "match" is determined by analyzing and comparing specific regions of DNA in two samples, such as an evidence sample found at a crime scene and a suspect's DNA sample. If the DNA profiles from the two samples are identical at the examined regions, a match is declared. The forensic investigators then calculate the probability of this match occurring by chance, considering the frequency of the observed DNA profile in the general population. Though DNA matches have significant value in criminal investigations, it is essential to acknowledge their limitations. If a DNA match is found, it does not mean the suspect is guilty but rather that the suspect should be investigated further. False matches can occur due to laboratory errors, cross-contamination, or the presence of identical twins. Additionally, the absence of a DNA match does not necessarily mean the suspect is innocent; it could indicate that evidence was lost or not found. It is crucial to consider the context and corroborate DNA evidence with other types of evidence to ensure a reliable verdict.

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Most popular questions from this chapter

Assume you have conducted a DNA sequencing reaction using the chain- termination (Sanger) method. You performed all the steps correctly and electrophoresced the resulting DNA fragments correctly, but when you looked at the sequencing gel, many of the bands were duplicated (in terms of length) in other lanes. What might have happened?

The human insulin gene contains a number of sequences that are removed in the processing of the mRNA transcript. In spite of the fact that bacterial cells cannot excise these sequences from mRNA transcripts, explain how a gene like this can be cloned into a bacterial cell and produce insulin.

A human cDNA clone was isolated from a cDNA library using a homologous mouse gene as a probe. The clone was grown in \(E\) coll, miniprepped to isolate the \(c D N A\), and then amplificd by \(\mathrm{PCR}\) using primers designed to the sequence of the mouse gene. When the PCR reaction was run on an agarose gel, there were multiple weak bands present instead of one clear band. What are the possible reasons for this result? How can the experiment be improved so that one clear band is amplified next time?

You have recovered a cloned DNA segment from a vector and determine that the insert is 1300 bp in length. To characterize this cloned segment, you isolate the insert and decide to construct a restriction map, Using enzyme I and enzyme II, followed by gel clectrophoresis, you determine the number and size of the fragments produced by enzymes I and II alone and in combination, as recorded in the following table. Construct a restriction map from these data, showing the positions of the restriction-enzyme cutting sites relative to one another and the distance between them in units of base pairs.

If you performed a PCR experiment starting with only one copy of double- stranded DNA, approximately how many DNA molecules would be present in the reaction tube after 15 cycles of amplification?

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