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chapter 1 - Bentham Science

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Neurohormones and Second Messengers in Lepidoptera HPFP: Recent Advances in Insects and Other Arthropods Vol. 1 113<br />

larvae of D. melanogaster has also been isolated using chromatographic techniques and amino acid<br />

sequence analysis [20], and is composed of A and B fragments, each consisting of 21 amino acid residues<br />

of about 2310 daltons each, linked to an oligosaccharide and arranged to form a glycopeptide of 66 KDa.<br />

Bombyx PTTH and Drosophila PTTHs are not chemically related and do not appear to be mutually<br />

antigenic [20]. Bombyxin resembles vertebrate insulin A, and can affect carbohydrate metabolism as well<br />

as other tasks [10] including induction of ecdysteroidogenesis in ovaries of the blowfly Phormia regina<br />

[22]. The structure of OEH, the larger brain factor that induces ovaries to synthesize ecdysteroid, was<br />

derived from a preparation of 6 million mosquito heads. It is a peptide composed of 31 amino acid residues<br />

(PTNVEMRCKLYSGPAVQNTGECVHGAELN), although longer sequences up to 108 residues and<br />

polymeric forms were also identified. No sequence similarity to the PTTHs was detected, although 29% of<br />

the OEH sequence resembled another insect neuropeptide, locust neuroparsin [14]. The sequence of LTE<br />

was derived from a homogenate of 13,000 brains of L. dispar pupae by using protein sequence analysis and<br />

electrospray mass spectrometry. The most prevalent fraction, active in inducing ecysteroid synthesis by<br />

testes from H. virescens and L. dispar, proved to be a 21 amino acid residue with a molecular weight of<br />

2473 da. Its molecular sequence was determined to be NH2-ISDFDEYEPLNDNDDDEVLDF-OH, [23-<br />

24]. An analog of TE stimulated ecdysteroid synthesis by cricket ovarian mesenteries [25] but was not<br />

active in eliciting ecdysteroid synthesis by prothoracic glands of either L. dispar or B. mori [cited in 24].<br />

Lymantria TE does not share any sequence with the large dimeric form of B. mori PTTH [19], nor was it<br />

immunologically interactive with the 66 KDa PTTH isolated from D. melanogaster [20] or Aedes aegypti<br />

OEH [14]. A U.S.National Institutes of Health peptide database (BLAST) search of Lymantria TE indicated<br />

homology with inhibitory peptides, such as those inhibiting cytolysis [26]. Fullbright et al [27] have shown<br />

that the Bombyx ovarian receptor for the prothoracicotropic hormone Bombyxin is similar to the<br />

mammalian insulin receptor, while Rewitz et al. [28] report that the prothoracotropic hormone receptor in<br />

Drosophila is a tyrosine kinase. Thus, the various steroidogenic peptides probably stimulate different<br />

receptors and/or physiological cascades in their respective target tissues even though the steroid hormones<br />

they induce in the various organs appear similar. The ecdysteroid hormones that are produced in each case<br />

may have local effects or play different roles at different times in development.<br />

Figure 2: Schematic diagram of sagittal (A) and frontal (B) view of the regions of the pupal central nervous system<br />

containing LTE-reactive cells and nerve tracts. AL: antennal lobe; AN: antennal nerve; CA: corpus allatum; CC: corpus<br />

cardiacum; E: esophagus; FC: frontal connectives; FG: frontal ganglion; LNC: lateral neurosecretory cells; MNC:<br />

medial neurosecretory cells; NCCI, II: nervi corporis cardiaci; OLC: optic lobe neurosecretory cells; P: protocerebrum;<br />

SG: subesophageal ganglion; T: tritocerebrum [18].

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