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Mol. Cell. Biol., 02 1997, 989-998, Vol 17, No. 2
ZB Mackey, W Ramos, DS Levin, CA Walter, JR McCarrey and AE Tomkinson
Three mammalian genes encoding DNA ligases have been identified. However,
the role of each of these enzymes in mammalian DNA metabolism has not been
established. In this study, we show that two forms of mammalian DNA ligase
III, alpha and beta, are produced by a conserved tissue-specific
alternative splicing mechanism involving exons encoding the C termini of
the polypeptides. DNA ligase III-alpha cDNA, which encodes a 103-kDa
polypeptide, is expressed in all tissues and cells, whereas DNA ligase
III-beta cDNA, which encodes a 96-kDa polypeptide, is expressed only in the
testis. During male germ cell differentiation, elevated expression of DNA
ligase III-beta mRNA is restricted, beginning only in the latter stages of
meiotic prophase and ending in the round spermatid stage. In 96-kDa DNA
ligase III-beta, the C- terminal 77 amino acids of DNA ligase III-alpha are
replaced by a different 17- to 18-amino acid sequence. As reported
previously, the 103-kDa DNA ligase III-alpha interacts with the DNA strand
break repair protein encoded by the human XRCC1 gene. In contrast, the
96-kDa DNA ligase III-beta does not interact with XRCC1, indicating that
DNA ligase III-beta may play a role in cellular functions distinct from the
DNA repair pathways involving the DNA ligase III-alpha x XRCC1 complex. The
distinct biochemical properties of DNA ligase III-beta, in combination with
the tissue- and cell-type-specific expression of DNA ligase III-beta mRNA,
suggest that this form of DNA ligase III is specifically involved in the
completion of homologous recombination events that occur during meiotic
prophase.
Copyright © 1997, American Society for Microbiology
An alternative splicing event which occurs in mouse pachytene spermatocytes generates a form of DNA ligase III with distinct biochemical properties that may function in meiotic recombination
Department of Molecular Medicine, Institute of Biotechnology, The University of Texas Health Science Center at San Antonio, 78245, USA.
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