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Ital. J. Zool., 66. 265-272 (1999)
Downloaded by [31.185.101.115] at 11:07 10 April 2016Genomic evolution in parental and INTRODUCTION
hybrid taxa of the genus Bacillus
(Insecta Phasmatodea) An ample series of investigations earned out by means
of morphological, karyological, and allozymatic ap-
BARBARA MANTOVANI proaches (Mantovani et al, 1997, and references therein)
MARCO PASSAMONTI demonstrated that the holo-Mediterranean genus Bacillus
VALERIO SCALI comprises the bisexuals B. rossius and B. grandii, the
Dipartimento di Biologia Evoluzionistica Sperimentale, unisexual B. atticus and, in Sicily, their related hybrids:
Università di Bologna, the diploids B. rossius-grandii and B. whitei, and the
via Selmi 3, I-40126 Bologna (Italy) triploid B. lynceorum (Figs 1, 2). These have been inves-
tigated also for their peculiar reproductive biology. Hy-
ABSTRACT brid taxa can actually reproduce by parthenogenesis (B.
whitei and B. lynceorum) or hybridogenesis and andro-
Fifteen-year-long investigations have demonstrated that bisexual genesis (B. rossius-grandii, Fig. 3). The genus Bacillus,
Bacillus species (B. rossius and B. grandii), although sharply dif- on the whole, constitutes a good example of reticulate
ferentiated for allozyme genes (Nei's D, 1.23-1.62), have hybridized evolution (Scali et al, 1995, and references therein).
several times in Sicily, generating hybridogenetic strains (B. rossius-
grandii) and parthenogenetic taxa, the diploid B. whitei (B. ros- The bisexual B. rossius (2n = 36, XX female; 35, X0
sius/B. grandii) and, together with the telytokous taxon B. atticus, male) ranges over most of the western Mediterranean
the triploid trihybrid B. lynceorum (B. rossius/B. grandii/B. atticus). basin with eight races mainly defined on the basis of
B. atticus is much closer to B. grandii (D, 0.31-0.36) than to B. ros- genetic distances obtained from gene-enzyme analyses.
sius (D = 1.82). Furthermore, SEM and allozymatic investigations Two such races are found in Italy: B. rossiusrossiusand
allowed it to be established that body and egg characters are more B. rossius redtenbacheri. The latter is widespread in
conserved than gene-enzyme systems. Recently, satellite DNA se- Sicily and represents the maternal ancestor of all Bacil-
quences (the Bag320 family) and a mitochondrial coding gene lus hybrids (see below). The strictly bisexual B. grandii
(COII) were also analysed. It could be noticed that Bag sequences (2n = 34, XX female; 33, X0 male) is endemic to the Si-
provided differentiation values among taxa higher than coding nu- cilian area and is differentiated into three formally de-
clear genes. Furthermore, it was discovered that, while partheno- scribed subspecies: B. grandii grandii located with a
genesis in B. atticus leaves random levels of individual variability few relict populations in the Iblean region; B. grandii
of repeats - likely due to the absence of chromosome shuffling in benazzii with demes scattered over a narrow coastal
the progeny -, the nucleotide sequences of B. grandii split into belt in northwestern Sicily and on the Island of Levanzo
subspecific clusters, indicating that sequence variant homogeniza- (Egadi Archipelago); B. grandii maretimi endemic to
tion/fixation are at work in Mendelian reproducing species. In B. the Island of Marettimo (Egadi Archipelago). Also the
whitei and B, lynceorum, only a limited sequence variability of all-female parthenogen B. atticus is differentiated into
grandii-like repeats was observed, that suggested a rather recent three races on the basis of allozyme and karyological
origin for them, although sufficiently old to allow gene-conversion characterization: the diploid B. atticus atticus (2n = 33-
to start between grandii-like and atticus-like sequences in B. 34) widely distributed in the central Mediterranean
lynceorum. The invention of both grandii-like and atticus-like Bag basin (Sardinia, Sicily, southern Italian peninsula, Croatia
320 clones also established beyond doubt the B. atticus contibu- and Greece); B. atticus carius including the Greek and
tion to the structure of this triploid hybrid. MtDNA of the COII Turkish triploid demes (3n = 48-51) and a single diploid
gene gave indications of a more homogeneous degree of differen- Turkish population (2n = 34); B. atticus cyprius (2n =
tiation among taxa than that suggested by nuclear compartments, 32) from the island of Cyprus (Scali et al, 1995).
since B. rossius,B. grandii, and B. atticus appear to be differentiat-
ed from each other to a similar degree. Furthermore, COII unex- Morphological features, karyotype characters and ge-
pectedly demonstrated that, in addition to hybridogens and B. netic distances on allozyme loci (Nei's D value = 0.31-
whitei, also B. lynceorum has B. rossius as the maternal ancestor, 0.36) point to a close relationship between the bisexual
thus indicating a hybridization route different from that previously B. grandii and the unisexual B. atticus. For the sake of
thought for this hybrid. Finally, mtDNA served as a genetic marker argument, it should be borne in mind, though, that
to demonstrate that androgenesis does occur in nature, since from parthenogenetic reproduction could have slowed down
hybridogenetic females, B. grandii specimens were produced, car- the differentiation in B. atticus. On the contrary, when
rying mtDNA of B. rossius.Androgens provide an unusual oppor- these two species are compared to B. rossiusa high de-
tunity of genome evolution since gene-size fragments of DNA can gree of differentiation emerges. This is well supported
escape from mitochondria and migrate to the nucleus. by several diagnostic morphological characters, high
Nei's distance values (Nei's D value = 1.23-1.62) and
KEY WORDS: Stick insects - Genome evolution - mtDNA - clear differences in karyotypes (Scali et al, 1995).
satDNA - Allozymes - Hybrid parentage - Parthenogenesis - Natur-
al androgenesis. Owing to the above-reported interspecific diver-
gences, the hybrid structure and the origin of the
ACKNOWLEDGEMENTS diploid unisexuals B. rossius-grandii and B. whitei
have been clearly traced and defined. Both hybridoge-
We appreciate the skilful suggestions made by Dr. Ombretta netic and parthenogenetic females derive from B. ros-
Marescalchi for egg maturation process drawing.
Invited paper at the Symposium on "Structure and Evolution of
Genome", 59th National Congress of the Unione Zoologica Ital-
iana held in San Benedetto del Tronto in September 1998.