Brock Biology of Microorganisms (14th Edition)
Brock Biology of Microorganisms (14th Edition)
14th Edition
ISBN: 9780321897398
Author: Michael T. Madigan, John M. Martinko, Kelly S. Bender, Daniel H. Buckley, David A. Stahl, Thomas Brock
Publisher: PEARSON
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Chapter 26.7, Problem 1MQ
Summary Introduction

Major histocompatibility complex is the group of genes that encode for proteins that are crucial for antigen presentation. This MHC gene is located on chromosome 6 and code for MHC protein. MHC proteins are classified into two classes MHC I and MHC II, these cell surface proteins recognize and bind with antigens from pathogens and present them to immune cells. MHCs regulate adaptive immune response.

The MHC proteins are called as human leukocyte antigens (HLAs) in case of humans. These proteins are responsible for antigen presentation to the T cell receptors. T cell receptors are formed by combination of three different complementarity determining regions CDR (1, 2 and 3).

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*Example 2: Tracing the path of an autosomal dominant trait Trait: Neurofibromatosis Forms of the trait: The dominant form is neurofibromatosis, caused by the production of an abnormal form of the protein neurofibromin. Affected individuals show spots of abnormal skin pigmentation and non-cancerous tumors that can interfere with the nervous system and cause blindness. Some tumors can convert to a cancerous form. i The recessive form is a normal protein - in other words, no neurofibromatosis.moovi A typical pedigree for a family that carries neurofibromatosis is shown below. Note that carriers are not indicated with half-colored shapes in this chart. Use the letter "N" to indicate the dominant neurofibromatosis allele, and the letter "n" for the normal allele. Nn nn nn 2 nn Nn A 3 N-
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