Problem 9
Question
Pedigree analysis is necessary when studying human inheritance patterns because ______________ a. humans have approximately 20,000 genes b. of ethical problems with experimenting on humans c. inheritance in humans is more complicated than it is in other organisms d. genetic disorders occur only in humans
Step-by-Step Solution
Verified Answer
The correct answer is b.
1Step 1: Understanding the Question
We need to identify why pedigree analysis is important for studying human inheritance patterns. We'll carefully examine each option to determine the most accurate reason.
2Step 2: Analyzing Option a
Option a states that humans have approximately 20,000 genes. While it's true that humans have many genes, this alone does not necessitate pedigree analysis for studying human inheritance patterns.
3Step 3: Considering Option b
Option b suggests that ethical problems with experimenting on humans make pedigree analysis necessary. This is an important reason because experimenting on humans for genetic studies presents ethical issues, making non-experimental methods like pedigree analysis vital.
4Step 4: Evaluating Option c
Option c claims that human inheritance is more complicated than in other organisms. While human inheritance can be complex, complexity itself isn't the primary reason for using pedigree analysis.
5Step 5: Reviewing Option d
Option d states that genetic disorders occur only in humans. This is incorrect, as genetic disorders can and do occur in other organisms as well.
6Step 6: Determining the Best Answer
The best answer is option b, as ethical concerns are a significant reason for using pedigree analysis in human genetic studies instead of direct experimentation.
Key Concepts
Human Inheritance PatternsEthical Issues in GeneticsGenetic DisordersNon-Experimental Methods
Human Inheritance Patterns
Understanding human inheritance patterns involves looking at how specific traits or diseases are passed down through family trees. This process is intricate, mainly because multiple factors can influence these patterns:
- Autosomal Dominant and Recessive: Traits could be dominant, appearing even if only one parent contributes them, or recessive, showing only when both parents pass on the gene.
- Sex-Linked Traits: Men and women can inherit traits differently based on chromosomes, particularly the X and Y chromosomes.
- Polygenic Traits: Characteristics like height or skin color depend on multiple genes instead of one.
Ethical Issues in Genetics
When it comes to genetic research, especially involving humans, ethical considerations are paramount. Experimenting directly on humans can pose significant ethical dilemmas because:
- It may harm participants or invade their privacy without clear consent.
- It could lead to discrimination if information about genetic disorders is misused.
- There’s a potential for eugenics, where the information might be used to promote selective breeding practices.
Genetic Disorders
Genetic disorders arise due to anomalies or mutations in an individual's DNA. They can affect people in various ways and are categorized based on their causes:
- Dominant Disorders: These appear if a person gets even one defective gene from a parent. Huntington's disease is an example.
- Recessive Disorders: Conditions like cystic fibrosis occur when both parents pass on a defective gene without showing any symptoms themselves.
- Chromosomal Disorders: These are caused by abnormalities in chromosome number or structure. Down syndrome is a well-known condition in this category.
Non-Experimental Methods
In genetic studies, non-experimental methods provide a way to gather valuable information without direct intervention. These methods include:
- Pedigree Analysis: As a tool to study inheritance, pedigrees display family relationships and track traits through the lineage, offering insights into genetic links and probability of disorders.
- Surveys and Questionnaires: Collection of genetic information or family histories through self-reported data assisting researchers in detecting patterns or correlations.
Other exercises in this chapter
Problem 7
One gene that gives rise to three traits is an example of ____________ a. polygenic inheritance b. codominance c. pleiotropy
View solution Problem 8
____________ in a trait is indicated by a bell curve. a. An epigenetic effect b. Nondisjunction c. Incomplete dominance d. Continuous variation
View solution Problem 11
Nondisjunction at meiosis can result in _____________ a. base-pair substitutions b. aneuploidy c. crossing over d. pleiotropy
View solution Problem 12
True or false? An individual with three or more complete sets of chromosomes is polyploid.
View solution