cDNA sequences and organization of IgM heavy chain genes in two holostean fish

Immunoglobulin M heavy chain (μ) sequences of two holostean fish, the bowfin, Amia calva, and the longnose gar, Lepisosteus osseus, were amplified from spleen mRNA by RACE-PCR, cloned, and sequenced. Each μ chain showed the conserved four constant domain structure typical of a secreted μ chain. Sout...

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Published in:Developmental and comparative immunology Vol. 19; no. 2; pp. 153 - 164
Main Authors: Wilson, Melanie R., Ravenstein, Eric van, Miller, Norman W., Clem, L.William, Middleton, Darlene L., Warr, Gregory W.
Format: Journal Article
Language:English
Published: United States Elsevier Ltd 01-03-1995
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Abstract Immunoglobulin M heavy chain (μ) sequences of two holostean fish, the bowfin, Amia calva, and the longnose gar, Lepisosteus osseus, were amplified from spleen mRNA by RACE-PCR, cloned, and sequenced. Each μ chain showed the conserved four constant domain structure typical of a secreted μ chain. Southern blot analyses with specific heavy chain variable (V H) and constant (C H) region probes suggest that both fish possess an IgH locus that resembles that of the teleosts, amphibians, and mammals in its organization. The overall sequence similarity of gar and bowfin μ chains was 60% and 48% at the nucleotide and amino acid levels, respectively, while similarity to the μ chains of teleosts and elasmobranchs was lower. The bowfin μ chain possesses a distinctive proline-rich sequence at the Cμ1/Cμ2 boundary; a shorter proline-rich sequence is present at this position in the gar μ chain. Both gar and bowfin show, in their Cμ4 sequences, motifs that could serve as cryptic splice donor sites for the production of mRNA encoding the membrane-bound form of the μ chains, and the bowfin also shows a potential cryptic splice donor site in the Cμ3 exon.
AbstractList Immunoglobulin M heavy chain (mu) sequences of two holostean fish, the bowfin, Amia calva, and the longnose gar, Lepisosteus osseus, were amplified from spleen mRNA by RACE-PCR, cloned, and sequenced. Each mu chain showed the conserved four constant domain structure typical of a secreted mu chain. Southern blot analyses with specific heavy chain variable (VH) and constant (CH) region probes suggest that both fish possess an IgH locus that resembles that of the teleosts, amphibians, and mammals in its organization. The overall sequence similarity of gar and bowfin mu chains was 60% and 48% at the nucleotide and amino acid levels, respectively, while similarity to the mu chains of teleosts and elasmobranchs was lower. The bowfin mu chain possesses a distinctive proline-rich sequence at the C mu 1/C mu 2 boundary; a shorter proline-rich sequence is present at this position in the gar mu chain. Both gar and bowfin show, in their C mu 4 sequences, motifs that could serve as cryptic splice donor sites for the production of mRNA encoding the membrane-bound form of the mu chains, and the bowfin also shows a potential cryptic splice donor site in the C mu 3 exon.
Immunoglobulin M heavy chain (μ) sequences of two holostean fish, the bowfin, Amia calva, and the longnose gar, Lepisosteus osseus, were amplified from spleen mRNA by RACE-PCR, cloned, and sequenced. Each μ chain showed the conserved four constant domain structure typical of a secreted μ chain. Southern blot analyses with specific heavy chain variable (V H) and constant (C H) region probes suggest that both fish possess an IgH locus that resembles that of the teleosts, amphibians, and mammals in its organization. The overall sequence similarity of gar and bowfin μ chains was 60% and 48% at the nucleotide and amino acid levels, respectively, while similarity to the μ chains of teleosts and elasmobranchs was lower. The bowfin μ chain possesses a distinctive proline-rich sequence at the Cμ1/Cμ2 boundary; a shorter proline-rich sequence is present at this position in the gar μ chain. Both gar and bowfin show, in their Cμ4 sequences, motifs that could serve as cryptic splice donor sites for the production of mRNA encoding the membrane-bound form of the μ chains, and the bowfin also shows a potential cryptic splice donor site in the Cμ3 exon.
Author Ravenstein, Eric van
Clem, L.William
Miller, Norman W.
Warr, Gregory W.
Middleton, Darlene L.
Wilson, Melanie R.
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  givenname: Melanie R.
  surname: Wilson
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  givenname: Eric van
  surname: Ravenstein
  fullname: Ravenstein, Eric van
  organization: Department of Microbiology, University of Mississippi Medical Center, Jackson, MS 39216-4505 U.S.A
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  surname: Miller
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  givenname: L.William
  surname: Clem
  fullname: Clem, L.William
  organization: Department of Microbiology, University of Mississippi Medical Center, Jackson, MS 39216-4505 U.S.A
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  givenname: Darlene L.
  surname: Middleton
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  givenname: Gregory W.
  surname: Warr
  fullname: Warr, Gregory W.
  organization: Department of Biochemistry and Molecular Biology, Medical University of South Carolina, Charleston, SC 29425-2211 U.S.A
BackLink https://www.ncbi.nlm.nih.gov/pubmed/7556802$$D View this record in MEDLINE/PubMed
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Keywords cDNA sequence
Gar
Bowfin
Immunoglobulin gene organization
Holostean fish
Language English
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Snippet Immunoglobulin M heavy chain (μ) sequences of two holostean fish, the bowfin, Amia calva, and the longnose gar, Lepisosteus osseus, were amplified from spleen...
Immunoglobulin M heavy chain (mu) sequences of two holostean fish, the bowfin, Amia calva, and the longnose gar, Lepisosteus osseus, were amplified from spleen...
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SubjectTerms Amino Acid Sequence
Animals
Base Sequence
Bowfin
cDNA sequence
DNA, Complementary - isolation & purification
Fishes - genetics
Gar
Holostean fish
Immunoglobulin Constant Regions - genetics
Immunoglobulin gene organization
Immunoglobulin Heavy Chains - genetics
Immunoglobulin M - genetics
Immunoglobulin mu-Chains - genetics
Molecular Sequence Data
Sequence Homology, Amino Acid
Sequence Homology, Nucleic Acid
Title cDNA sequences and organization of IgM heavy chain genes in two holostean fish
URI https://dx.doi.org/10.1016/0145-305X(94)00063-L
https://www.ncbi.nlm.nih.gov/pubmed/7556802
https://search.proquest.com/docview/77609324
Volume 19
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