TY - JOUR
T1 - Expression pattern of a butterfly achaete-scute homolog reveals the homology of butterfly wing scales and insect sensory bristles
AU - Galant, Ron
AU - Skeath, James B.
AU - Paddock, Steve
AU - Lewis, David L.
AU - Carroll, Sean B.
N1 - Funding Information:
We thank Jayne Selegue and Julie Gates for technical assistance, Grace Panganiban for the Tribolium AS-C gene homolog sequence, Georg Halder for comments on the manuscript, and Jamie Wilson for help on its preparation. R.G. is a National Institutes of Health Predoctoral Trainee in Genetics; J.B.S. is supported by the Cancer Research Fund of the Damon Runyon-Walter Winchell Foundation Award, DRS-9, a Howard Hughes Medical Institute Research Resources Program for Medical Schools Junior Faculty Award #76296-538202, and by National Institute of Neurological Disorders and Stroke grant, RBI-NS36570; S.B.C. is supported by National Science Foundation grant IBN-9418499 and is an Investigator of the Howard Hughes Medical Institute. In memory of Tony Bladl.
PY - 1998/7/2
Y1 - 1998/7/2
N2 - Background: Lepidopteran wing scales are the individual units of wing color patterns and were a key innovation during Lepidopteran evolution. On the basis of developmental and morphological evidence, it has been proposed that the sensory bristles of the insect peripheral nervous system and the wing scales of Lepidoptera are homologous structures. In order to determine if the developmental pathways leading to Drosophila sensory bristle and butterfly scale formation use similar genetic circuitry, we cloned, from the butterfly Precis coenia, a homolog of the Drosophila achaete-scute (AS-C) genes - which encode transcription factors that promote neural precursor formation - and examined its expression pattern during development. Results: During embryonic and larval development, the expression pattern of the AS-C homolog, ASH1, forecasted neural precursor formation. ASH1 was expressed both in embryonic proneural clusters - within which an individual cell retained ASH1 expression, enlarged, segregated, and became a neural precursor - and in larval wing discs in putative sensory mother cells. ASH1 was also expressed in pupal wings, however, in evenly spaced rows of enlarged cells that had segregated from the underlying epidermis but, rather than give rise to neural structures, each cell contributed to an individual scale. Conclusions: ASH1 appears to perform multiple functions throughout butterfly development, apparently promoting the initial events of selection and formation of both neural and scale precursor cells. The similarity in the cellular and molecular processes of scale and neural precursor formation suggests that the spatial regulation of an AS-C gene was modified during Lepidopteran evolution to promote scale cell formation.
AB - Background: Lepidopteran wing scales are the individual units of wing color patterns and were a key innovation during Lepidopteran evolution. On the basis of developmental and morphological evidence, it has been proposed that the sensory bristles of the insect peripheral nervous system and the wing scales of Lepidoptera are homologous structures. In order to determine if the developmental pathways leading to Drosophila sensory bristle and butterfly scale formation use similar genetic circuitry, we cloned, from the butterfly Precis coenia, a homolog of the Drosophila achaete-scute (AS-C) genes - which encode transcription factors that promote neural precursor formation - and examined its expression pattern during development. Results: During embryonic and larval development, the expression pattern of the AS-C homolog, ASH1, forecasted neural precursor formation. ASH1 was expressed both in embryonic proneural clusters - within which an individual cell retained ASH1 expression, enlarged, segregated, and became a neural precursor - and in larval wing discs in putative sensory mother cells. ASH1 was also expressed in pupal wings, however, in evenly spaced rows of enlarged cells that had segregated from the underlying epidermis but, rather than give rise to neural structures, each cell contributed to an individual scale. Conclusions: ASH1 appears to perform multiple functions throughout butterfly development, apparently promoting the initial events of selection and formation of both neural and scale precursor cells. The similarity in the cellular and molecular processes of scale and neural precursor formation suggests that the spatial regulation of an AS-C gene was modified during Lepidopteran evolution to promote scale cell formation.
UR - http://www.scopus.com/inward/record.url?scp=0032474896&partnerID=8YFLogxK
U2 - 10.1016/S0960-9822(98)70322-7
DO - 10.1016/S0960-9822(98)70322-7
M3 - Article
C2 - 9663389
AN - SCOPUS:0032474896
SN - 0960-9822
VL - 8
SP - 807
EP - 813
JO - Current Biology
JF - Current Biology
IS - 14
ER -