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Arrb1
Mus musculus
Rattus norvegicus
Homo sapiens
Bos taurus
Xenopus laevis
Danio rerio
b Arr1
Homo sapiens
chr.11
b Arr1
Mus musculus
chr.7
Rattus norvegicus
b Arr1
chr.1
b Arr1
Xenopus tropicalis
GL174850.1
GL173361.1
GL173305.1
GL172913.1
b rrb1
Danio rerio
chr.10
chr.15
chr.21
Arrb2
Xenopus laevis
Xenopus tropicalis
Danio rerio_a
Danio rerio_b
B os taurus
M us musculus
Rattus norvegicus
Homo sapiens
Homo sapiens
b Arr2
chr.17
Mus musculus
b Arr2
chr.11
Rattus norvegicus
b Arr2
Xenopus tropicalis
b Arr2
GL172659.1
GL173518.1
GL173293.1
b Arr2b
Danio rerio
chr.5
chr.7
chr.23
b Arr2a
chr.10
Figure 9.1 Conservation of vertebrate b-arrestins (barrs). Phylogenetic and synteny
analyses show the significant conservation of vertebrate arrestins. However, the phylo-
genetic analyses clearly indicate that barrs from aquatic species are somewhat distinct
from mammalian barrs. Upper panel: Comparison of barr1 (Arrb1) in different species.
On the chromosomal level, evolutionary conservation of b arr1 can be seen. The frag-
mented appearance of the Xenopus and zebrafish locus is due to the partially assembled
genomes in these species. Lower panels: comparison of barr2 (Arrb2). Note that in
zebrafish, the
b arr2
gene is duplicated.
with reduced expression of the glucocorticoid receptor. 9,10 Consistent with
these findings, mice deficient in glucocorticoid receptors die perinatally of
respiratory failure, 11 similar to the
arr1/2 double KO mice. Furthermore,
glucocorticoid receptors in the lung epithelium have been implicated in the
production of surfactant. 12 At present, however, little is known about the
signaling defects involved in the perinatal lethality of
b
b
arr1/2 double KO
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