A polycystic kidney-disease gene homologue required for male mating behaviour in C-elegans

Citation
Mm. Barr et Pw. Sternberg, A polycystic kidney-disease gene homologue required for male mating behaviour in C-elegans, NATURE, 401(6751), 1999, pp. 386-389
Citations number
30
Categorie Soggetti
Multidisciplinary,Multidisciplinary,Multidisciplinary
Journal title
NATURE
ISSN journal
00280836 → ACNP
Volume
401
Issue
6751
Year of publication
1999
Pages
386 - 389
Database
ISI
SICI code
0028-0836(19990923)401:6751<386:APKGHR>2.0.ZU;2-G
Abstract
The stereotyped mating behaviour of the Caenorhabditis elegans male is made up of several substeps: response, backing, turning, vulva location, spicul e insertion and sperm transfer. The complexity of this behaviour is reflect ed in the sexually dimorphic anatomy and nervous system(1). Behavioural fun ctions have been assigned to most of the male-specific sensory neurons by m eans of cell ablations; for example, the hook sensory neurons HOA and HOB a re specifically required for vulva location(2). We have investigated how se nsory perception of the hermaphrodite by the C. elegans male controls matin g behaviours. Here we identify a gene, lov-1 (for location of vulva), that is required for two male sensory behaviours: response and vulva location. l ov-1 encodes a putative membrane protein with a mucin-like, serine-threonin e-rich amino terminus' followed by two blocks of homology to human polycyst ins, products of the autosomal dominant polycystic kidney-disease loci PKD1 and PKD2 (ref 4). LOV-1 is the closest C. elegans homologue of PKD1. lov-1 is expressed in adult males in sensory neurons of the rays, hook and head, which mediate response, vulva location, and potentially chemotaxis to herm aphrodites, respectively(2,5). PKD-2, the C. elegans homologue of PKD2, is localized to the same neurons as LOV-1, suggesting that they function in th e same pathway.