1 However, oskar has only been identified in
holometabolous ("
higher") insects that specify their ger
2 We review recent and older work on
holometabolous insect development that sheds light on th
3 ar results were obtained in the more derived
holometabolous insect Drosophila melanogaster, suggestin
4 utionary derived state restricted to several
holometabolous insect lineages.
5 body reorganization during metamorphosis in
holometabolous insect species outside of the Diptera.
6 or, was identified and investigated in three
holometabolous insect species: Drosophila melanogaster,
7 -stranded RNA-mediated silencing, in a basal
holometabolous insect, the beetle Tribolium castaneum.
8 A key regulatory gene in metamorphosing (
holometabolous)
insect life histories is the transcripti
9 phology of the CSD neurons originated in the
holometabolous insects (those that undergo complete meta
10 mentation LXXLL motif was stably acquired in
holometabolous insects after the appearance of striped e
11 may reflect evolutionary changes within the
holometabolous insects and serves as a model to study in
12 We considered OXPHOS genes of six
holometabolous insects and their orthologs from three Na
13 Corresponding events in
holometabolous insects are simplified and lack formal na
14 This essential role of E93 is conserved in
holometabolous insects as TcE93 RNAi in Tribolium castan
15 The timely onset of metamorphosis in
holometabolous insects depends on their reaching the app
16 During metamorphosis,
holometabolous insects eliminate obsolete larval tissues
17 In
holometabolous insects growth ends at the onset of metam
18 Experiments in Drosophila and other
holometabolous insects have demonstrated that either dam
19 Metamorphosis in
holometabolous insects is an ecdysone-dependent process
20 The ventral nerve cord of
holometabolous insects is reorganized during metamorphos
21 Holometabolous insects like Drosophila proceed through t
22 The neuromuscular systems of
holometabolous insects must be remodeled during metamorp
23 r subsequent transformation to appendages in
holometabolous insects remains elusive at the developmen
24 Adult structures in
holometabolous insects such as Drosophila are generated
25 have been studied functionally in only a few
holometabolous insects that undergo metamorphosis.
26 Our data suggest that in ancestral
holometabolous insects the female Dsx form is the defaul
27 tus of mosquitoes, flies, and possibly other
holometabolous insects to be monitored.
28 (~345 Ma), and the major diversification of
holometabolous insects to the Early Cretaceous.
29 Holometabolous insects undergo complete metamorphosis to
30 that the larval visual organs (stemmata) of
holometabolous insects were derived from and are therefo
31 nes occur only in Tribolium and not in other
holometabolous insects with a sequenced genome.
32 In
holometabolous insects, a species-specific size, known a
33 mplicated in many developmental processes in
holometabolous insects, but its mechanism of signaling r
34 e situation exists in first instar larvae of
holometabolous insects, in which absence of UbdA express
35 inherited germ plasm, in contrast with many
holometabolous insects, including Drosophila.
36 he tobacco hornworm Manduca sexta, like many
holometabolous insects, makes two versions of its thorac
37 s a wide variety of biological activities in
holometabolous insects, ranging from vitellogenesis and
38 In
holometabolous insects, segment identity may be specifie
39 ntrasts with the more evolutionarily derived
holometabolous insects, such as the honey bee and the fr
40 In
holometabolous insects, the adult appendages and interna
41 ult metamorphosis in both hemimetabolous and
holometabolous insects, thus acting as the universal adu
42 has led to the successful diversification of
holometabolous insects, yet the origin of the pupa remai
43 to its well-known essential germline role in
holometabolous insects.
44 jor events, including the diversification of
holometabolous insects.
45 use thus provides a reference for studies of
holometabolous insects.
46 in Drosophila melanogaster, and possibly all
holometabolous insects.
47 portant role in the evolution of the pupa in
holometabolous insects.
48 re sparsely known compared with more derived
holometabolous insects.
49 iation was present in the common ancestor of
holometabolous insects.
50 ifera, a member of the most basal lineage of
holometabolous insects.
51 ocation originated in the common ancestor of
holometabolous insects.
52 ents the ancestral form of CNS patterning in
Holometabolous insects.
53 esis seen in the larva-to-pupa transition of
holometabolous insects.
54 estigated during adult muscle development in
holometabolous insects.
55 ila well describe embryogenesis of advanced,
holometabolous,
insects generally.
56 ment in hemimetabolous insects suggests that
holometabolous metamorphosis combines patterning process
57 d several times in different lineages of the
holometabolous,
or fully metamorphosing, insects.
58 tion rates only occurred in the four richest
holometabolous orders.