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MAJOR HISTOCOMPATIBILITY
COMPLEX & HEAT SHOCK
PROTEIN
IN CHICKEN
Dr.S.Sivaramakrishnan
MVM15032(PSC)
DepartmentofPoultryScience
MadrasVeterinaryCollege
MHC
(Major histocompatibility complex)
A large cluster of linked genes located in
some chromosome of chicken, encode for MHS
and relate to immune response, immune
regulation and cell-cell recognition.
History
• MHC is a group of highly conserved genes defined by its
influence on tissue graft acceptance.
• MHC was discovered in the 1930s by Peter Gorer in his
pioneering studies of antigenic responses to transplanted
sera by inbred mouse strains (Gorer 1936)
• The chicken was the second animal species in which the
MHC was identified (Schierman and Nordskog, 1961)
• Chicken MHC has been designated as the B complex
because of its linkage with the B blood group (Briles et al.,
1950)
MHC function
MHC Peptides
Pathogen
T Cell
 Present antigen to initiate immune response with a phenomena
known as MHC restriction
 Endogenous Ag is presented to CD8+ T cell by MHC class Ⅰ
molecule
 Exogenous Ag is presented to CD4+ T cell by MHC class Ⅱ
molecule
 Participant in both humoral and cell-mediated immunity
 Act as antigen presenting structures
Biological function of MHC
Properties of MHC
1. MHC is polygenic it contains several
different MHC class I and MHC class II
genes - different ranges of peptide-binding
specificities.
2. MHC is highly polymorphic – multiple
variants of each gene within the population as
a whole.
– Class I MHC genes (B-F)
• Glycoproteins expressed on all nucleated cells
• Major function to present processed Ags to TC
– Class II MHC genes (B-L)
• Glycoproteins expressed on M, B-cells, Monocytes
• Major function to present processed Ags to TH
MHC Classes
– Class III MHC genes
• Products that include secreted proteins that have immune
functions. Ex. Complement system, inflammatory molecules
- Class IV MHC genes (B-G)
• expressed on erythrocytes and other cells such as liver cells, bursal and
thymic lymphoblast and stromal cells.
• The class IV MHC is involved in antibody response, which is supposed to
involve B cell repertoire and the B cell antigen recognition and binding
• The other unique MHC linked gene in the avian, is
the Rfp-Y that is recognised by DNA restriction
fragment pattern (Rfp) of the MHC class I, II and IV
genes in one MHC haplotype
1
3
2
MHC-encoded -chain of 43kDa
Structure of MHC class I molecules
3 domain & 2m have structural & amino acid sequence
homology with Ig G domains Ig GENE SUPERFAMILY
2m
2-microglobulin, 12kDa, non-MHC encoded, non-
transmembrane, non covalently bound to -chain
Peptide antigen in a groove formed
from a pair of -helicies on a floor of anti-
parallel  strands
-chain anchored to the cell membrane
2
1
and a -chain of 29kDa
MHC-encoded, -chain of 34kDa
2
1
Structure of MHC class II molecules
 and  chains anchored to the cell membrane
2 & 2 domains have structural & amino acid sequence
homology with Ig G domains Ig GENE SUPERFAMILY
No -2 microglobulin
Peptide antigen in a groove formed from a pair of -helicies
on a floor of anti-parallel  strands
MHC and immune response
MHC molecules interact with both the foreign
antigen and with complementary structure of
other immune cells, thereby generating an
immune response that is specific for the
inducing antigen
The T-/B-cell co-operation necessary for
antibody production and for the generation of
germinal centres in the spleen requires identity
at the MHC
Interaction of APCs and T cells, evaluated by
the in vitro proliferation of T cells in response
to specific antigen in the presence of APCs, is
also MHC-restricted.
The B-F/B-L antigens are the restriction
elements for all of these cellular interaction
phenomena.
The MHC effects on genetic control of immuno-
responsiveness, either due to restriction element
or through specific MHC-linked immune response
genes.
Antibody production against a variety of antigens,
such as immune response to synthetic
polypeptides, is linked to the chicken MHC
(Gunther et al., 1974)
Complement proteins are extremely important
in the immune reaction as a means to destroy
invading pathogens.
The levels of total serum haemolytic
complement have been associated with the
MHC in chickens.
MHC and disease resistance
 MHC – resistance to a specific disease concerns Marek's disease
(MD), a herpesvirus-induced lymphoma.
 Using MHC recombinants to the B-F/B-L region, partial MHC control
has been mapped.
 The MHC is associated with MD-related traits of incidence of tumour
formation, mortality and transient paralysis induced by MDV.
 The haplotype B21 conveys MD resistance to many different genetic
backgrounds.
 Variation in response to MDV by sublines that are identical at the B
locus, however, illustrates the influence of non-MHC genes on
response to MD (Bacon L.D. - 1987)
Selected diseases for which an association of resistance or
severity is found with the chicken MHC
Type of disease Disease
Neoplastic diseases (virally induced) Marek's disease neoplasia
Marek's disease transient paralysis
Rous' sarcomas
Lymphoid leucosis
Bacterial diseases Staphylococcus aureus
Fowl cholera (Pasteurella multocida)
Salmonella enteritidis
Parasitic diseases (coccidiosis) Eimeria tenella
Eimeria acervulina
Autoimmune diseases Autoimmune thyroiditis
Chicken MHC and production traits
 Economically important traits, such as juvenile and adult
mortality, body weight, fertilization rate, embryonic
mortality, hatchability and egg production are influenced
by MHC genotype (Bacon L.D. - 1987)
 Several independent studies have shown that long-term
selection for egg production traits and disease resistance
have significantly altered MHC allelic frequencies (Gavora
et al., 1986)
 From these selection studies, B2 and B21 appeared to show
overall beneficial associations with economic traits in
chickens.
• Birds which were aneuploid (trisomic) for the
MHC-bearing chromosome were used to map
the MHC to microchromosome 16 and to
examine the effects of MHC gene dosage on
several biological systems.
Selected production traits for which an association with the
MHC is found
Production traits
Body weight
Juvenile survival
Adult survival
Egg production
Hatchability
Embryonic mortality
Fertilization rate
Applications of MHC manipulation to the poultry
industry
 Differences between MHC types can be identified by
using serological blood typing or by restriction fragment
length polymorphism analysis of DNA and can be utilized
in several ways by the breeding industry.
 An MHC (or B blood group) allele can be used as a
pedigree marker, if it is unique to a genetic line within a
company, and thus can identify that line and any
accidental crosses made with it.
 MHC manipulation is to alter the frequency of alleles
in the population to improve associated traits such as
disease resistance, immune response and production
traits (Lamont, 1989).
 Future industrial applications of MHC manipulation
may include alteration of the gene copy number in
individual animals by use of natural variation or genetic
engineering (Bloom et al., 1988).
HEAT SHOCK PROTEINS(HSP)
History
• HSP Discovered in 1962 Ferruccio Ritossa (1936-
2014)
• chromosomes of salivary glands in Drosophila
melanogaster larva
• Heat shock proteins are highly conserved
molecules that are present, and can be induced, in
all eukaryotic and prokaryotic species, including
plants
Functions
• The primary function of these proteins is to govern the
folding and refolding mechanism of native and stress
denatured proteins.
• Unfolded polypeptides, prevent their aggregation and
thereby, potentiate the folding process.
• Hsps are also involved in diverse cellular roles such as
protein assembly, translocation and degradation.
• Hence these proteins are the essential determinants of
protein quality control in cell.
Classification
Based on their molecular mass and function, HSPs
are classified into six families namely;
1. Small Heat Shock Proteins (sHsp/Hsp20),
2. Hsp40 (J-class proteins),
3. Hsp60 (Caperonin),
4. Hsp70,
5. Hsp90,
6. Hsp100 proteins
Temp
environ
Temp
cell
Folded
Proteins
Unfolded
Proteins Aggregates
Loss of Protein
Function
Network
failure
Death
Cell
Need for HSP
HSP Synthesis
• Transcription of HSP genes is mediated by the
interaction of heat shock factor (HSF)
• Chickens, four HSFs have been identified
• HSF1 and HSF2 are ubiquitously expressed and
conserved.
• HSF1 – physiological and environmental stress
• HSF2 – mostly induced during differentiation and
early development.
• HSF1 - present in the cytoplasm as a latent monomeric molecule
that is unable to bind to DNA.
• When exposed to stress, an intracellular flux of newly
synthesised non-native proteins activates HSF1
(hyperphosphorylated)
• HSF1 is converted to phosphorylated trimers that have the
capacity to bind DNA, and which translocate from the cytoplasm
to the nucleus.
• HSF2 has the characteristics of a temperature-sensitive protein; it
is inactivated when exposed to raised temperature, and
sequestered to the cytoplasm, and is thereby prevented from
interference with HSF1 activity in stressed cells.
Major family Intracellular localisation Intracellular function
Hsp27 Cytoplasm/nucleus Actin dynamics
Hsp32 Cytoplasm Haem catabolism, antioxidant of properties
Hsp40 Cytoplasm/nucleus Regulates the activity of Hsp70; binds non-native
Proteins
Hsp47 ER Processing of pro-collagen; processing and/or secretion of
collagen
Hsp60 Mitochondria Bind to partly folded polypeptides and assist correct
folding. Assembly of multimeric complexes
Hsp70
HSP Location and Function
Hsp70 Cytoplasm/nucleus Bind to extended polypeptides. Prevent aggregation
of unfolded peptides. Dissociate some oligomers.
ATP binding. ATPase activity. Hsp70 downregulates
HSF1 activity
Hsp90 Cytoplasm Bind to other proteins. Regulate protein activity.
Prevent aggregation of refolded peptide. Correct
assembly and folding of newly synthesised protein.
Hsp90 assists the maintenance of the HSF1
monomeric state in non- stressful conditions.
Hsp110
(human)
Nucleolus/cytoplasm Thermal tolerance
Hsp105 Cytoplasm Protein refolding
HSPs in antigen presentation by MHC class I/II
molecules
HSPs and autoimmunity
• HSPs, particularly Hsp60 and Hsp70, are highly
immunogenic capable of inducing antibody production and
T cell activation.
• The antibodies and T cells against bacterial Hsp60 and
Hsp70 also recognize chicken Hsp60 and Hsp70
respectively, as a result of cross reactivity.
• These anti-Hsp60 and anti-Hsp70 anti- bodies and T cells
injure tissues and cause inflammatory reactions. Thus,
Hsp60 and Hsp70 have been implicated in the pathogenesis
of a number of autoimmune diseases and inflammatory
conditions.
HSP influenced on immunity
HSP on specific immunity
HSP in Disease resistance
• Zulkifli et al., 1994a and Liew et al., 2003. They reported
that stress due to neonatal feed restriction can improve
resistance to marble spleen disease and infectious bursal
disease in feed restricted chickens in comparison to those
fed ad libitum.
• Solemani et al., 2012 stated that 60% feed restriction and
60% feed restriction plus quercetin (1500mg/kg) from day 4
to 6. Resulted that both the groups had significantly lower
Salmonella enteritidis colonization and lower HSP70
expression then that of controlled chickens
• Zulkifli et al., 2003. conducted a trial on 36 days old
birds was administered 10 times the normal dose of live
IBD vaccine. After heat exposure , the Feed Restricted
Heat treatment birds had higher HSP70 density and
weight gain and lower bursal histological score then
their heat treatment and control birds. They concluded
that Feed Restricted Heat treatment could improve
weight gain and resistance to Infectious Bursal Disease
in male broiler chickens
HSP in Heat tolerance
• Yahav et al. (1997) reported that exposure to acute heat
stress resulted in enhanced synthesis of heat shock protein.
Synthesis of heat shock protein induced to a lesser extent in
tissues of broiler chicken, which acquired improved heat
tolerance, than in tissues of control chickens.
• Azim (2012) observed that exposing chicks to heat
treatment at 40ºC for 4 hours daily during the first 14 days.
He reported to improve the heat tolerance of broilers
through heat treatment during the first two weeks.
• Yahav and McMurtry (2001) found that thermal conditioning
of chicks results in improvements in performance and heat
tolerance at marketing age. He resulted thermal conditioning is
growth retardation followed by an immediate compensatory
growth period, which resulted in complete compensation for
the loss of weight gain, and lead to higher body weight of the
conditioned chickens at 42 day of age.
Conclusions
• MHC and HSP are highly conserved genes. MHC mainly acts on immune
regulation.
• HSP are extremely potent molecules, importance for physiological and
immunological process is indicated by the high degree to which their
structure and function are phylogenetically conserved.
• Through the gene mapping to develop the disease resistance breeds.
• In native chicken like Aseel are more disease resistant due to the highly
expression of MHC genes compared to commercial chicken. Likewise HSP
in native chickens highly expressed in stress conditions compared to
commercial chickens so that mortality also low in native chickens.
• Both MHC and HSP genes used to increase the production traits of the
chicken.
Major Histocompatibility Complex & Heat Shock Protein in Chicken

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Major Histocompatibility Complex & Heat Shock Protein in Chicken

  • 1. MAJOR HISTOCOMPATIBILITY COMPLEX & HEAT SHOCK PROTEIN IN CHICKEN Dr.S.Sivaramakrishnan MVM15032(PSC) DepartmentofPoultryScience MadrasVeterinaryCollege
  • 2. MHC (Major histocompatibility complex) A large cluster of linked genes located in some chromosome of chicken, encode for MHS and relate to immune response, immune regulation and cell-cell recognition.
  • 3. History • MHC is a group of highly conserved genes defined by its influence on tissue graft acceptance. • MHC was discovered in the 1930s by Peter Gorer in his pioneering studies of antigenic responses to transplanted sera by inbred mouse strains (Gorer 1936) • The chicken was the second animal species in which the MHC was identified (Schierman and Nordskog, 1961) • Chicken MHC has been designated as the B complex because of its linkage with the B blood group (Briles et al., 1950)
  • 5.  Present antigen to initiate immune response with a phenomena known as MHC restriction  Endogenous Ag is presented to CD8+ T cell by MHC class Ⅰ molecule  Exogenous Ag is presented to CD4+ T cell by MHC class Ⅱ molecule  Participant in both humoral and cell-mediated immunity  Act as antigen presenting structures Biological function of MHC
  • 6. Properties of MHC 1. MHC is polygenic it contains several different MHC class I and MHC class II genes - different ranges of peptide-binding specificities. 2. MHC is highly polymorphic – multiple variants of each gene within the population as a whole.
  • 7. – Class I MHC genes (B-F) • Glycoproteins expressed on all nucleated cells • Major function to present processed Ags to TC – Class II MHC genes (B-L) • Glycoproteins expressed on M, B-cells, Monocytes • Major function to present processed Ags to TH MHC Classes
  • 8. – Class III MHC genes • Products that include secreted proteins that have immune functions. Ex. Complement system, inflammatory molecules - Class IV MHC genes (B-G) • expressed on erythrocytes and other cells such as liver cells, bursal and thymic lymphoblast and stromal cells. • The class IV MHC is involved in antibody response, which is supposed to involve B cell repertoire and the B cell antigen recognition and binding
  • 9. • The other unique MHC linked gene in the avian, is the Rfp-Y that is recognised by DNA restriction fragment pattern (Rfp) of the MHC class I, II and IV genes in one MHC haplotype
  • 10. 1 3 2 MHC-encoded -chain of 43kDa Structure of MHC class I molecules 3 domain & 2m have structural & amino acid sequence homology with Ig G domains Ig GENE SUPERFAMILY 2m 2-microglobulin, 12kDa, non-MHC encoded, non- transmembrane, non covalently bound to -chain Peptide antigen in a groove formed from a pair of -helicies on a floor of anti- parallel  strands -chain anchored to the cell membrane
  • 11. 2 1 and a -chain of 29kDa MHC-encoded, -chain of 34kDa 2 1 Structure of MHC class II molecules  and  chains anchored to the cell membrane 2 & 2 domains have structural & amino acid sequence homology with Ig G domains Ig GENE SUPERFAMILY No -2 microglobulin Peptide antigen in a groove formed from a pair of -helicies on a floor of anti-parallel  strands
  • 12.
  • 13. MHC and immune response MHC molecules interact with both the foreign antigen and with complementary structure of other immune cells, thereby generating an immune response that is specific for the inducing antigen
  • 14. The T-/B-cell co-operation necessary for antibody production and for the generation of germinal centres in the spleen requires identity at the MHC
  • 15. Interaction of APCs and T cells, evaluated by the in vitro proliferation of T cells in response to specific antigen in the presence of APCs, is also MHC-restricted. The B-F/B-L antigens are the restriction elements for all of these cellular interaction phenomena.
  • 16. The MHC effects on genetic control of immuno- responsiveness, either due to restriction element or through specific MHC-linked immune response genes. Antibody production against a variety of antigens, such as immune response to synthetic polypeptides, is linked to the chicken MHC (Gunther et al., 1974)
  • 17. Complement proteins are extremely important in the immune reaction as a means to destroy invading pathogens. The levels of total serum haemolytic complement have been associated with the MHC in chickens.
  • 18. MHC and disease resistance  MHC – resistance to a specific disease concerns Marek's disease (MD), a herpesvirus-induced lymphoma.  Using MHC recombinants to the B-F/B-L region, partial MHC control has been mapped.  The MHC is associated with MD-related traits of incidence of tumour formation, mortality and transient paralysis induced by MDV.  The haplotype B21 conveys MD resistance to many different genetic backgrounds.  Variation in response to MDV by sublines that are identical at the B locus, however, illustrates the influence of non-MHC genes on response to MD (Bacon L.D. - 1987)
  • 19. Selected diseases for which an association of resistance or severity is found with the chicken MHC Type of disease Disease Neoplastic diseases (virally induced) Marek's disease neoplasia Marek's disease transient paralysis Rous' sarcomas Lymphoid leucosis Bacterial diseases Staphylococcus aureus Fowl cholera (Pasteurella multocida) Salmonella enteritidis Parasitic diseases (coccidiosis) Eimeria tenella Eimeria acervulina Autoimmune diseases Autoimmune thyroiditis
  • 20. Chicken MHC and production traits  Economically important traits, such as juvenile and adult mortality, body weight, fertilization rate, embryonic mortality, hatchability and egg production are influenced by MHC genotype (Bacon L.D. - 1987)  Several independent studies have shown that long-term selection for egg production traits and disease resistance have significantly altered MHC allelic frequencies (Gavora et al., 1986)  From these selection studies, B2 and B21 appeared to show overall beneficial associations with economic traits in chickens.
  • 21. • Birds which were aneuploid (trisomic) for the MHC-bearing chromosome were used to map the MHC to microchromosome 16 and to examine the effects of MHC gene dosage on several biological systems.
  • 22. Selected production traits for which an association with the MHC is found Production traits Body weight Juvenile survival Adult survival Egg production Hatchability Embryonic mortality Fertilization rate
  • 23. Applications of MHC manipulation to the poultry industry  Differences between MHC types can be identified by using serological blood typing or by restriction fragment length polymorphism analysis of DNA and can be utilized in several ways by the breeding industry.  An MHC (or B blood group) allele can be used as a pedigree marker, if it is unique to a genetic line within a company, and thus can identify that line and any accidental crosses made with it.
  • 24.  MHC manipulation is to alter the frequency of alleles in the population to improve associated traits such as disease resistance, immune response and production traits (Lamont, 1989).  Future industrial applications of MHC manipulation may include alteration of the gene copy number in individual animals by use of natural variation or genetic engineering (Bloom et al., 1988).
  • 26. History • HSP Discovered in 1962 Ferruccio Ritossa (1936- 2014) • chromosomes of salivary glands in Drosophila melanogaster larva • Heat shock proteins are highly conserved molecules that are present, and can be induced, in all eukaryotic and prokaryotic species, including plants
  • 27. Functions • The primary function of these proteins is to govern the folding and refolding mechanism of native and stress denatured proteins. • Unfolded polypeptides, prevent their aggregation and thereby, potentiate the folding process. • Hsps are also involved in diverse cellular roles such as protein assembly, translocation and degradation. • Hence these proteins are the essential determinants of protein quality control in cell.
  • 28. Classification Based on their molecular mass and function, HSPs are classified into six families namely; 1. Small Heat Shock Proteins (sHsp/Hsp20), 2. Hsp40 (J-class proteins), 3. Hsp60 (Caperonin), 4. Hsp70, 5. Hsp90, 6. Hsp100 proteins
  • 29. Temp environ Temp cell Folded Proteins Unfolded Proteins Aggregates Loss of Protein Function Network failure Death Cell Need for HSP
  • 30.
  • 31. HSP Synthesis • Transcription of HSP genes is mediated by the interaction of heat shock factor (HSF) • Chickens, four HSFs have been identified • HSF1 and HSF2 are ubiquitously expressed and conserved. • HSF1 – physiological and environmental stress • HSF2 – mostly induced during differentiation and early development.
  • 32. • HSF1 - present in the cytoplasm as a latent monomeric molecule that is unable to bind to DNA. • When exposed to stress, an intracellular flux of newly synthesised non-native proteins activates HSF1 (hyperphosphorylated) • HSF1 is converted to phosphorylated trimers that have the capacity to bind DNA, and which translocate from the cytoplasm to the nucleus. • HSF2 has the characteristics of a temperature-sensitive protein; it is inactivated when exposed to raised temperature, and sequestered to the cytoplasm, and is thereby prevented from interference with HSF1 activity in stressed cells.
  • 33.
  • 34. Major family Intracellular localisation Intracellular function Hsp27 Cytoplasm/nucleus Actin dynamics Hsp32 Cytoplasm Haem catabolism, antioxidant of properties Hsp40 Cytoplasm/nucleus Regulates the activity of Hsp70; binds non-native Proteins Hsp47 ER Processing of pro-collagen; processing and/or secretion of collagen Hsp60 Mitochondria Bind to partly folded polypeptides and assist correct folding. Assembly of multimeric complexes Hsp70 HSP Location and Function
  • 35. Hsp70 Cytoplasm/nucleus Bind to extended polypeptides. Prevent aggregation of unfolded peptides. Dissociate some oligomers. ATP binding. ATPase activity. Hsp70 downregulates HSF1 activity Hsp90 Cytoplasm Bind to other proteins. Regulate protein activity. Prevent aggregation of refolded peptide. Correct assembly and folding of newly synthesised protein. Hsp90 assists the maintenance of the HSF1 monomeric state in non- stressful conditions. Hsp110 (human) Nucleolus/cytoplasm Thermal tolerance Hsp105 Cytoplasm Protein refolding
  • 36. HSPs in antigen presentation by MHC class I/II molecules
  • 37.
  • 38. HSPs and autoimmunity • HSPs, particularly Hsp60 and Hsp70, are highly immunogenic capable of inducing antibody production and T cell activation. • The antibodies and T cells against bacterial Hsp60 and Hsp70 also recognize chicken Hsp60 and Hsp70 respectively, as a result of cross reactivity. • These anti-Hsp60 and anti-Hsp70 anti- bodies and T cells injure tissues and cause inflammatory reactions. Thus, Hsp60 and Hsp70 have been implicated in the pathogenesis of a number of autoimmune diseases and inflammatory conditions.
  • 39. HSP influenced on immunity
  • 40. HSP on specific immunity
  • 41. HSP in Disease resistance • Zulkifli et al., 1994a and Liew et al., 2003. They reported that stress due to neonatal feed restriction can improve resistance to marble spleen disease and infectious bursal disease in feed restricted chickens in comparison to those fed ad libitum. • Solemani et al., 2012 stated that 60% feed restriction and 60% feed restriction plus quercetin (1500mg/kg) from day 4 to 6. Resulted that both the groups had significantly lower Salmonella enteritidis colonization and lower HSP70 expression then that of controlled chickens
  • 42. • Zulkifli et al., 2003. conducted a trial on 36 days old birds was administered 10 times the normal dose of live IBD vaccine. After heat exposure , the Feed Restricted Heat treatment birds had higher HSP70 density and weight gain and lower bursal histological score then their heat treatment and control birds. They concluded that Feed Restricted Heat treatment could improve weight gain and resistance to Infectious Bursal Disease in male broiler chickens
  • 43. HSP in Heat tolerance • Yahav et al. (1997) reported that exposure to acute heat stress resulted in enhanced synthesis of heat shock protein. Synthesis of heat shock protein induced to a lesser extent in tissues of broiler chicken, which acquired improved heat tolerance, than in tissues of control chickens. • Azim (2012) observed that exposing chicks to heat treatment at 40ºC for 4 hours daily during the first 14 days. He reported to improve the heat tolerance of broilers through heat treatment during the first two weeks.
  • 44. • Yahav and McMurtry (2001) found that thermal conditioning of chicks results in improvements in performance and heat tolerance at marketing age. He resulted thermal conditioning is growth retardation followed by an immediate compensatory growth period, which resulted in complete compensation for the loss of weight gain, and lead to higher body weight of the conditioned chickens at 42 day of age.
  • 45. Conclusions • MHC and HSP are highly conserved genes. MHC mainly acts on immune regulation. • HSP are extremely potent molecules, importance for physiological and immunological process is indicated by the high degree to which their structure and function are phylogenetically conserved. • Through the gene mapping to develop the disease resistance breeds. • In native chicken like Aseel are more disease resistant due to the highly expression of MHC genes compared to commercial chicken. Likewise HSP in native chickens highly expressed in stress conditions compared to commercial chickens so that mortality also low in native chickens. • Both MHC and HSP genes used to increase the production traits of the chicken.

Editor's Notes

  1. 1. MHC molecules is to bind peptide fragments derived from pathogens and display them on the cell surface for recognition by the appropriate T cells
  2. Figure 1: induction and regulation of heat shock protein expression Physical or chemical stress induces production of unfolded or misfolded proteins. Heat shock factor monomers in the cytoplasm form trimers, are phosphorylated, and translocate into the nucleus. HSF homotrimers bind to heat shock protein gene promoter regions, leading to induction of Hsp gene transcription. Hsp70 gene transcription is downregulated by interaction of Hsp70 or HSBP1 with the HSF trimers.
  3. (a)In non-APCs, endogenous proteins are proteolytically cleaved in the cytosol and (b)the resulting peptides are chaperoned by the HSPs that protect, transport and deliver them to TAP. (c)The peptides are introduced by HSPs to TAP and are introduced via TAP into the ER; (d)there, they are received by a different set of HSPs. (e)These HSPs participate in antigen processing and loading onto MHC class I molecules destined for the cell surface. (f)Upon stress or death, HSPs of the ER and cytosol gain access to the extracellular space
  4. (g)there, they encounter APCs that express specific receptors such as CD91. (h)Interaction of HSP−peptide complexes with CD91 leads to receptor-mediated endocytosis, processing of the antigenic peptide by the endogenous MHC class I pathway and (i)re-presentation on the cell surface. (j)Additionally, HSPs may activate professional APCs, through CD91 or other receptors, to stimulate secretion of proinflammatory cytokines and upregulation of co-stimulatory molecules