scholarly journals MHC genes in Invertebrates: The Echinodermata

2019 ◽  
Vol 2 (4) ◽  
pp. 102-105
Author(s):  
Leclerc Michel ◽  
◽  
Jolly Ariane ◽  
de la Grange Pierre ◽  
◽  
...  

The MHC is a set of genes that codes for cell surface proteins essential for the acquired immune system to recognize foreign molecules in vertebrates and MHC II gene was described in Echinodermata for the first time. For the present time, MHC Class I gene was not found in a significant manner so for concluding the existence of MHC I gene in Echinodermata, further studies will be necessarily done.

2021 ◽  
Vol 2021 ◽  
pp. 1-14
Author(s):  
Muhammad Usman Ghani ◽  
Li Bo ◽  
An Buyang ◽  
Xu Yanchun ◽  
Shakeel Hussain ◽  
...  

In vertebrate animals, the molecules encoded by major histocompatibility complex (MHC) genes play an essential role in the adaptive immunity. MHC class I deals with intracellular pathogens (virus) in birds. MHC class I diversity depends on the consequence of local and global environment selective pressure and gene flow. Here, we evaluated the MHC class I gene in four species of the Turdidae family from a broad geographical area of northeast China. We isolated 77 MHC class I sequences, including 47 putatively functional sequences and 30 pseudosequences from 80 individuals. Using the method based on analysis of cloned amplicons ( n = 25 ) for each species, we found two and seven MHC I sequences per individual indicating more than one MHC I locus identified in all sampled species. Results revealed an overall elevated genetic diversity at MHC class I, evidence of different selection patterns among the domains of PBR and non-PBR. Alleles are found to be divergent with overall polymorphic sites per species ranging between 58 and 70 (out of 291 sites). Moreover, transspecies alleles were evident due to convergent evolution or recent speciation for the genus. Phylogenetic relationships among MHC I show an intermingling of alleles clustering among the Turdidae family rather than between other passerines. Pronounced MHC I gene diversity is essential for the existence of species. Our study signifies a valuable tool for the characterization of evolutionary relevant difference across a population of birds with high conservational concerns.


Science ◽  
1993 ◽  
Vol 260 (5112) ◽  
pp. 1320-1322 ◽  
Author(s):  
T. Howcroft ◽  
K Strebel ◽  
M. Martin ◽  
D. Singer

2000 ◽  
Vol 51 (6) ◽  
pp. 491-495 ◽  
Author(s):  
A. Sato ◽  
Holger Sültmann ◽  
Werner E. Mayer ◽  
Jan Klein

1990 ◽  
Vol 31 (5-6) ◽  
pp. 405-409 ◽  
Author(s):  
Guido Kroemer ◽  
Rima Zoorob ◽  
Charles Auffray

Blood ◽  
1991 ◽  
Vol 78 (2) ◽  
pp. 524-532 ◽  
Author(s):  
RA Zeff ◽  
YF Zhao ◽  
R Tatake ◽  
H Lachman ◽  
F Borriello ◽  
...  

Abstract Numerous tumor cell lines of leukemic origin are known to modulate cell surface expression of major histocompatibility complex (MHC) class I antigens resulting in alterations in their immune detection and tumorigenicity. We have been studying the mechanisms responsible for attenuation of MHC class I gene expression in an H-2 heterozygous (H-2b x H-2d) Abelson-Murine leukemia virus (A-MuLV)-transformed leukemic cell line (designated R8). Here we report that treatment of the R8 cell line with the protein synthesis inhibitor cycloheximide (CHX) increased H-2Kb steady-state messenger RNA (mRNA) levels several fold. The induced H-2Kb mRNA transcripts were functional, as demonstrated by their ability to be translated into immunoprecipitable H-2Kb alloantigen. H-2Kb null variants derived from the R8 cell line were shown to be the product of both cis- and trans-acting mechanisms, insomuch as the treatment of R8-derived H-2Kb non-expressor lines with CHX re-established expression of H-2Kb mRNA to the same extent as transfection of the variant cell line with the wild-type H-2Kb gene. Such findings indicate that downregulation of MHC class I gene expression is constitutive for the R8 leukemic cell line, a phenomenon that may be related to the immature pre-B-cell phenotype of this A-MuLV transformant.


2002 ◽  
Vol 3 (1) ◽  
pp. 20-24 ◽  
Author(s):  
D Lio ◽  
C R Balistreri ◽  
G Colonna-Romano ◽  
M Motta ◽  
C Franceschi ◽  
...  

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