Abstract
Poly(A)RNAs prepared from the thymuses of C57BL/6J and DBA/2J mice were used to construct cDNA libraries in the bacterial expression vector lambda gt11. The libraries were scanned first for protein production with polyvalent antiserum prepared against the 73kDa gag protein of mouse intracisternal A-particles (IAP). Reactive plaques were crossed-screened by hybridization with an IAP-specific DNA probe. Two IAP-specific protein-producing plaques were obtained from the C57BL/6 library and 4 from the DBA/2 library. One C57BL/6 cDNA clone (B12) and two DBA cDNA clones (D8 and D20) were sequenced in their entirety. Clones B12 and D8 were remarkably similar, particularly when compared to the 6 other IAP elements that have been sequenced thus far. We discuss the evidence which leads us to suggest that these clones may be derived from allelic IAP elements expressed in mouse thymus.
MeSH Terms
Alleles
Amino Acid Sequence
Animals
Base Sequence
DNA/genetics
Gene Expression Regulation
Gene Products, gag
Genes, Intracisternal A-Particle
Mice
Mice, Inbred C57BL/genetics
Mice, Inbred DBA/genetics
Poly A/genetics,isolation & purification
Proto-Oncogenes
RNA, Messenger/genetics,isolation & purification
Retroviridae Proteins/biosynthesis,genetics
Sequence Homology, Nucleic Acid
Thymus Gland/analysis
Chemicals
Gene Products, gag
RNA, Messenger
Retroviridae Proteins
Poly A
DNA
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Grossman Z
Mietz J A
Kuff E L
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