Allele-specific expression analysis reveals CD79B has a cis-acting regulatory element that responds to Marek's disease virus infection in chickens


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Meydan H., YILDIZ M. A., Dodgson J. B., Cheng H. H.

POULTRY SCIENCE, cilt.90, sa.6, ss.1206-1211, 2011 (SCI-Expanded) identifier identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 90 Sayı: 6
  • Basım Tarihi: 2011
  • Doi Numarası: 10.3382/ps.2010-01295
  • Dergi Adı: POULTRY SCIENCE
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Sayfa Sayıları: ss.1206-1211
  • Anahtar Kelimeler: Marek's disease, genetic resistance, allele-specific expression, CD79B, growth hormone, AFFECTING SUSCEPTIBILITY, GENE-EXPRESSION, IDENTIFICATION, RESISTANCE, COMPLEX, PROTEIN, SCREEN, CELLS
  • Akdeniz Üniversitesi Adresli: Hayır

Özet

Marek's disease (MD) is a T cell lymphoma disease of domestic chickens induced by the Marek's disease virus (MDV), a highly infectious and naturally oncogenic alphaherpesvirus. Enhancing genetic resistance to MD in poultry is an attractive method to augment MD vaccines, which protect against MD but do not prevent MDV replication and horizontal spread. Previous work integrating QTL scans, transcript profiling, and MDV-chicken protein-protein interaction screens revealed 3 MD resistance genes; however, a major challenge continues to be the identification of the other contributing genes. To aid in this search, we screened for allele-specific expression (ASE) in response to MDV infection, a simple and novel method for identifying polymorphic cis-acting regulatory elements, which may contain strong candidate genes with specific alleles that confer MD genetic resistance. In this initial study, we focused on immunoglobulin beta (CD79B) because it plays a critical role in the immune response and, more important, is transcriptionally coupled with growth hormone (GH1), one of the previously identified MD resistance genes. Using a coding SNP in CD79B and pyrosequencing to track the relative expression of each allele, we monitored ASE in uninfected and MDV-infected F(1) progeny from reciprocal intermatings of highly inbred chicken lines 6(3) (MD resistant) and 7(2) (MD susceptible). Upon screening 3 tissues (bursa, thymus, and spleen) at 5 time points (1, 4, 7, 11, and 15 d postinfection), we observed that MDV infection alters the CD79B allelic ratios in bursa and thymus tissues at 4 and 15 d postinfection in both mating directions. Our results suggest that CD79B has a cis-acting regulatory element that responds to MDV infection and probably cooperates with GH1 in conferring genetic resistance to MD. This result helps validates the use of ASE screens to identify specific candidate genes for complex traits such as genetic resistance to MD.

Marek’s disease (MD) is a T cell lymphoma
disease of domestic chickens induced by the Marek’s
disease virus (MDV), a highly infectious and naturally
oncogenic alphaherpesvirus. Enhancing genetic resistance
to MD in poultry is an attractive method to augment
MD vaccines, which protect against MD but do
not prevent MDV replication and horizontal spread.
Previous work integrating QTL scans, transcript profiling,
and MDV–chicken protein–protein interaction
screens revealed 3 MD resistance genes; however, a
major challenge continues to be the identification of
the other contributing genes. To aid in this search, we
screened for allele-specific expression (ASE) in response
to MDV infection, a simple and novel method for identifying
polymorphic cis-acting regulatory elements,
which may contain strong candidate genes with specific
alleles that confer MD genetic resistance. In this initial
study, we focused on immunoglobulin β (CD79B)
because it plays a critical role in the immune response
and, more important, is transcriptionally coupled with
growth hormone (GH1), one of the previously identified
MD resistance genes. Using a coding SNP in CD79B
and pyrosequencing to track the relative expression
of each allele, we monitored ASE in uninfected and
MDV-infected F1 progeny from reciprocal intermatings
of highly inbred chicken lines 63 (MD resistant) and
72 (MD susceptible). Upon screening 3 tissues (bursa,
thymus, and spleen) at 5 time points (1, 4, 7, 11, and 15
d postinfection), we observed that MDV infection alters
the CD79B allelic ratios in bursa and thymus tissues at
4 and 15 d postinfection in both mating directions. Our
results suggest that CD79B has a cis-acting regulatory
element that responds to MDV infection and probably
cooperates with GH1 in conferring genetic resistance to
MD. This result helps validates the use of ASE screens
to identify specific candidate genes for complex traits
such as genetic resistance to MD.