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Ch. 14 - Analysis of Gene Function via Forward Genetics and Reverse Genetics
Sanders - Genetic Analysis: An Integrated Approach 3rd Edition
Sanders3rd EditionGenetic Analysis: An Integrated ApproachISBN: 9780135564172Not the one you use?Change textbook
Chapter 14, Problem C.11a

Go to the website http://www.ncbi.nlm.nih.gov/omim and enter 'Lynch syndrome' in the Search box at the top of the page. From the list of options given, select '#120435—Lynch Syndrome.' Use the information you retrieve to answer the following questions. There are two types of Lynch syndrome. What are they?

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Understand that Lynch syndrome is a hereditary condition associated with a high risk of colorectal cancer and other cancers, caused by mutations in DNA mismatch repair genes.
Go to the website http://www.ncbi.nlm.nih.gov/omim and enter 'Lynch syndrome' in the search box to access detailed genetic information about the condition.
From the search results, select the entry labeled '#120435—Lynch Syndrome' to view the specific OMIM record for this disorder.
Read through the summary and clinical features sections of the OMIM entry to identify the classification or types of Lynch syndrome described.
Note that the two main types of Lynch syndrome are typically distinguished based on the specific genes involved or clinical presentation, such as Lynch syndrome type I and type II, and record their definitions as provided.

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Key Concepts

Here are the essential concepts you must grasp in order to answer the question correctly.

Lynch Syndrome Overview

Lynch syndrome is an inherited disorder that increases the risk of colorectal cancer and other cancers due to mutations in DNA mismatch repair genes. Understanding its genetic basis helps explain why affected individuals have a higher cancer risk and guides diagnosis and management.
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Overview of Transcription

Types of Lynch Syndrome

Lynch syndrome is classified into two main types based on the specific genes involved and clinical features: Lynch syndrome type I primarily involves colorectal cancer, while Lynch syndrome type II includes a broader spectrum of associated cancers such as endometrial and ovarian cancers.
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Types of Maternal Inheritance

Use of OMIM Database

The Online Mendelian Inheritance in Man (OMIM) database is a comprehensive resource for genetic information. It provides detailed entries on genetic disorders like Lynch syndrome, including gene mutations, clinical features, and classification, which are essential for accurate understanding and research.
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Bioinformatics
Related Practice
Textbook Question

You have identified a gene encoding the protein involved in the rate-limiting step in vitamin E biosynthesis. How would you create a transgenic plant producing large quantities of vitamin E in its seeds?

Textbook Question

Go to the website http://www.ncbi.nlm.nih.gov/omim and enter 'Lynch syndrome' in the Search box at the top of the page. From the list of options given, select '#120435—Lynch Syndrome.' Use the information you retrieve to answer the following questions. What genes are most commonly mutated in Lynch syndrome?

Textbook Question

Go to the website http://www.ncbi.nlm.nih.gov/omim and enter 'Lynch syndrome' in the Search box at the top of the page. From the list of options given, select '#120435—Lynch Syndrome.' Use the information you retrieve to answer the following questions. What are the approximate rates of cancer that develop in people carrying a mutation of one of these genes?

Textbook Question

Go to the website http://www.ncbi.nlm.nih.gov/omim and enter 'Lynch syndrome' in the Search box at the top of the page. From the list of options given, select '#120435—Lynch Syndrome.' Use the information you retrieve to answer the following questions. Provide a brief summary of the normal functions of the protein products of these genes.

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Textbook Question

You have identified a recessive mutation that alters bristle patterning in Drosophila and have used recombinant DNA technology to identify a genomic clone that you believe harbors the gene. How would you demonstrate that your gene is on the genomic clone?

Textbook Question

Genetic counseling has not been discussed in this chapter, but it is a service provided by trained professional counselors who also have detailed knowledge of medical genetics, as described in Application Chapter A. Genetic counselors provide details about gene mutations and have knowledge of most of the details of diseases associated with genetic abnormalities. With regard to genetic testing to identify one's personal risk of cancer, what are the three or four topics you think are most important to be able to discuss with a genetic counselor?

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