Chapter 21 The Genetic Control of Animal Development
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Transcript Chapter 21 The Genetic Control of Animal Development
The Differentiation of
Vertebrate Immune Cells
In the immune system, two types of cells participate
directly in defense against pathogens.
Plasma B cells produce and secrete immunoglobulins
(antibodies), and killer T cell produce membranebound proteins that act as receptors for various
substances.
B cell antibodies and T cell receptors bind to specific
antigens. A cell must make many varieties of these
proteins because there are many potential
pathogens.
An Antigen-Antibody Complex
Structure of an Antibody Molecule
Human Antibody Genes
Two light chain loci: the on
chromosome 2 and on
chromosome 22
One heavy chain locus on
chromosome 14.
Each locus consists of a long array
of gene segments.
Gene Segments for a Kappa
Polypeptide
1.
An LV gene segment, encoding a leader peptide,
which is removed later, and the N-terminal 95
amino acids of the variable region of the kappa light
chain. (76 gene segments in humans; 40 of these
are functional)
2.
A J gene segment, encoding the last 13 amino
acids of the variable region of the kappa light chain.
(5 gene segments in humans)
3.
A C gene segment, encoding the constant region
of the kappa light chain. (1 gene segment in
humans)
The Kappa Locus
During B cell development, the kappa light
chain gene that will be expressed is
assembled from one LV segment, one J
segment, and the C segment by somatic
recombination.
Segment joining is mediated by recombination signal
sequences adjacent to each gene segment by a
protein complex including RAG1 and RAG2
(recombination activating gene proteins 1 and 2).
Many Different Antibodies Can
Be Produced
40 LV segments 5 J segments 1 C segment
= 200 kappa light chains.
Recombination of gene segments can create
120 lambda light chains and 6600 different
heavy chains.
Combinatorial assembly of these allows
production of 2,112,000 different antibodies.
Even more antibodies are possible due to
variation in recombination sites and
hypermutability of the variable regions.
Evidence for DNA Rearrangement
During Immune Cell Differentiation