Molecular Biology and Evolution, Vol 13, 767-779, Copyright © 1996 by Society for Molecular Biology and Evolution
LC Samuelson, RS Phillips and LJ Swanberg
Amylase transcription in the human salivary gland results from the
evolutionary juxtaposition of two inserted elements, a gamma-actin
pseudogene and an endogenous retrovirus, to create an unusual salivary-
specific promoter. We utilized these structures as molecular tags to
characterize the amylase genes in extant primates by polymerase chain
reaction amplification of promoter fragments from genomic DNA. Six distinct
amylase promoter structures were identified, which allowed us to infer the
structures of common ancestors and trace the evolution of the modern human
amylase promoters. Our data show that integration of the pseudogene and
retrovirus were evolutionarily recent events. The gamma-actin pseudogene
integrated after the divergence of the New World monkeys from the primate
ancestral tree, and the retrovirus integrated later, after the divergence
of the Old World monkeys. The New World monkey amylase promoter represents
the mammalian amylase precursor structure before integration of the two
retroposons. Two distinct amylase genes were identified in the Old World
monkeys, one with a complete gamma-actin pseudogene insert and another
novel structure with a truncation of the gamma-actin sequences. We
demonstrated abundant amylase expression in the saliva of an Old World
monkey, indicating that the endogenous retrovirus is not required for
amylase transcription in the primate salivary gland.
ORIGINAL ARTICLE
Amylase gene structures in primates: retroposon insertions and promoter evolution
Department of Physiology, University of Michigan.
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