Cytogenet Cell Genet 87:182–188 (1999)
Evolutionary disruptions of human syntenic
groups 3, 12, 14, and 15 in Ateles paniscus
chamek (Platyrrhini, Primates)
F.C. Canavez,
a
M.A.M. Moreira,
b
C.R. Bonvicino,
b
P. Parham,
a
and
H.N. Seua ´ nez
b, c
a
Department of Structural Biology, Stanford University School of Medicine, Stanford, CA (USA);
b
Genetics Section, Instituto Nacional de Câncer, Rio de Janeiro (Brazil); and
c
Department of Genetics, Universidade Federal do Rio de Janeiro, Rio de Janeiro (Brazil)
Supported by the Instituto Nacional de Câncer, Fundaça ˜o Ary Frauzino, Fundaça ˜o O
Botica ´ rio de Proteça ˜o à Natureza, and Fundaça ˜o de Amparo a Pesquisa do
Estado do Rio de Janeiro (Brazil), and by Grant No. AI 31168 from the National
Institutes of Health.
Received 2 July 1999; revision accepted 3 September 1999.
Request reprints from Dr. Héctor N. Seua ´ nez, Genetics Section,
Instituto Nacional de Câncer, Praça da Cruz Vermelha, 23,
20230-130 Rio de Janeiro, RJ (Brazil);
telephone: +55-21-506-6209; e-mail: genetics@inca.org.br.
ABC
Fax + 41 61 306 12 34
E-mail karger@karger.ch
www.karger.com
© 2000 S. Karger AG, Basel
0301–0171/99/0874–0182$17.50/0
Accessible online at:
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Abstract. Comparative gene assignments of 18 markers,
based on analyses of somatic cell hybrids and previous data in
the literature, indicated that human (HSA) syntenic groups 3,
12, 14, and 15 are dissociated in the spider monkey species
Ateles paniscus chamek (APC). Markers present in HSA 3p
were allocated to APC 3 and APC 9. The HSA 12 cluster was
split into two syntenic groups, one mainly including HSA 12p
markers in APC 16 and the other, including HSA 12q markers,
in APC 2p. The HSA 14q cluster split into three syntenic
groups, corresponding to APC 2q, APC 6, and APC 12. Finally,
the HSA 15 cluster split into two syntenic groups, APC 2q and
APC 3. Comparisons with previous gene assignments and
human SROs led to the tentative postulation of rearrangements
having occurred during the evolutionary divergence of man
and A. paniscus chamek. Chromosome painting data in the
congeneric species A. geoffroyi, other New World and Old
World primates, and several representative non-primate ani-
mals were compared in an attempt to delineate the ancestral
and derived conditions underlying the evolutionary rearrange-
ment of syntenic groups in mammals.
Copyright © 2000 S. Karger AG, Basel
Different extents of karyotypic rearrangements have taken
place during the phyletic radiation of mammals, resulting in
disparate syntenic assortments among mammalian orders
(O’Brien et al., 1988). Thus, while rodents are extremely shuf-
fled, karyotypic evolution in the primates has been more con-
servative, except in selected groups where rearrangements have
been prominent, as in the case of gibbons (among Old World
primates) and of owl, howler, and spider monkeys (among New
World primates).
Among the 15 or 16 extant genera of New World (neotropi-
cal) primates, the genus Ateles (2n = 32/34) was shown to be
greatly rearranged by karyotypic comparison with species be-
longing to other primate genera, including man (Turleau et al.,
1974; Seua ´ nez et al., 1993). This was later demonstrated by gene
assignment with primate × rodent cell hybrid panels showing
numerous disruptions of evolutionary conserved syntenic clus-
ters and de novo associations in Ateles paniscus chamek (2n =
34; Seua ´ nez et al., 1994, 1997; Moreira et al., 1997; Canavez et
al., 1998, 1999). Moreover, in the karyotypically similar congen-
eric species A. geoffroyi (2n = 34), chromosome painting with
human whole-chromosome probes (Morescalchi et al., 1997)
clearly showed a high amount of karyotypic shuffling that was
congruent with the syntenic associations previously described in
A. paniscus chamek. Taken together, these studies supported the
proposition that Ateles is a very derived primate lineage, as dem-
onstrated by cladistic analyses of DNA sequences of the Â-globin,
Á
1
-globin, and interstitial retinol-binding protein genes (Meireles
et al., 1995; Schneider et al., 1996).