EVOLUTION OF THE LARVAL CUTICLE PROTEINS CODED BY THE SECONDARY SEX-CHROMOSOME PAIR - X2 AND NEO-Y OF DROSOPHILA-MIRANDA .2. COMPARISON AT THE AMINO-ACID-SEQUENCE LEVEL
M. Steinemann et al., EVOLUTION OF THE LARVAL CUTICLE PROTEINS CODED BY THE SECONDARY SEX-CHROMOSOME PAIR - X2 AND NEO-Y OF DROSOPHILA-MIRANDA .2. COMPARISON AT THE AMINO-ACID-SEQUENCE LEVEL, Journal of molecular evolution, 43(4), 1996, pp. 413-417
The larval cuticle proteins (LCPs) are encoded by a multigene family,
Lcp1-4, located at the right arm of the metacentric autosome 2 (2R) in
Drosophila melanogaster. Due to a chromosome fusion the Lcp locus of
Drosophila miranda is situated on a pair of secondary sex chromosomes,
the X2 and neo-Y chromosomes. Comparing the deduced amino acid sequen
ces of the autosomal D. melanogaster loci with the sex-chromosomal loc
i of D. miranda, we were able to trace the evolution of the Lcp loci w
ith respect to their different chromosomal inheritance. The length of
the signal peptide is conserved in all four LCPs, while the size of th
e mature LCPs varies. Conserved protein motifs became obvious from the
alignment, indicating regions of structural and functional importance
. Analyzing intra- and interspecific sequence similarities of the Lcp
gene families allowed us to reconstruct the phylogeny of the gene clus
ter. Alignment with cuticle amino acid sequences originating from dive
rgent insect species reveals motifs already present in the primordial
insect LCPs. These motifs indicate different levels of constraint acti
ng during the evolution of the LCPs.