Searchable abstracts of presentations at key conferences in endocrinology

ea0022p255 | Comparative endocrinology | ECE2010

Pituitary adenylate cyclase-activating polypeptide related peptide (PRP) in an Anabantidae fish: its mRNA expression in the brain during gonadal development and sexual behavior and its hypophysiotropic effect on pituitary hormonal gene expression

Levy Gal , Gothilf Yoav , Degani Gad

Pituitary adenylate cyclase activating polypeptide - related peptide (PRP) (formerly known as growth hormone releasing hormone-like peptide GHRHLP) can act as a hypophysiotropic factor in several teleosts by stimulating growth hormone (GH) secretion. However, as yet, no information on this peptide as a regulator of reproduction exists. Recently, the full-length PRP cDNA was cloned in the blue gourami (Trichogaster trichopterus) and was found to be expressed in the brain...

ea0049oc8.2 | Neuroendocrinology | ECE2017

Knocking down/out the prokineticin pathway during zebrafish development results in the GnRH neurons axons misguiding

Bassi Ivan , Marelli Federica , Vezzoli Valeria , Persani Luca , Gothilf Yoav , Bonomi Marco

Studies conducted using knockout mouse model revealed that defects of PROKR2 affect the correct ontogeny of GnRH neurons and, by consequence, neuroendocrine control of reproduction. Nevertheless its exact role during these processes and in the pathogenesis of congenital hypogonadotropic hypogonadism (CHH) remains elusive due to the phenotypic differences observed between mouse and human. Zebrafish (ZF) has emerged in the last ten years as a reliable model organism for studying...

ea0041oc5.5 | Neuroendocrinology | ECE2016

Zebrafish tool for the study of prokineticin receptor 2 (PROKR2) pathway on GNRH3 neuronal development

Bassi Ivan , Marelli Federica , Vezzoli Valeria , Persani Luca , Gothilf Yoav , Bonomi Marco

The G protein-coupled receptor PROKR2 play an important and not fully understood role in GnRH-secreting neurons physiology. Indeed, mutations of PROKR2 in humans are known to cause Congenital Hypogonadotropic Hypogonadism (CHH) although with an important reproductive and olfactory phenotypic heterogeneity. The attempt to mimic PROKR2 human allelic variants in mouse model has so far failed to give insights into the mechanisms involved. The zebrafish (ZF), due to its amenability...

ea0039oc5.1 | Oral Communications 5 | BSPED2015

Mutations in IGSF10 cause self-limited delayed puberty

Howard Sasha , Guasti Leonardo , Ruiz-Babot Gerard , Mancini Alessandra , David Alessia , Storr Helen , Metherell Louise , Cabrera Claudia , Warren Helen , Barnes Michael , Wehkalampi Karoliina , Gothilf Yoav , Andre Valentina , Cariboni Anna , Dunkel Leo

Background: Abnormal pubertal timing affects over 4% of adolescents and is associated with adverse health and psychosocial outcomes. Previous studies estimate that 60–80% of variation in the timing of pubertal onset is genetically determined. However, despite this strong heritability, little is known about the genetic control of human puberty. Self-limited delayed puberty (DP) segregates in an autosomal dominant pattern, but in the majority of patients the neuroendocrine ...

ea0038oc1.2 | Early Career Oral Communications | SFEBES2015

Mutations in IGSF10 cause self-limited delayed puberty, via disturbance of GnRH neuronal migration

Howard Sasha , Guasti Leo , Ruiz-Babot Gerard , Mancini Alessandra , David Alessia , Storr Helen , Metherell Louise , Sternberg Michael , Cabrera Claudia , Warren Helen , Barnes Michael , Wehkalampi Karoliina , Andre Valentina , Gothilf Yoav , Cariboni Anna , Dunkel Leo

Background: Timing of puberty is associated with height, cardiovascular health and cancer risk, with a significant public health impact. Previous studies estimate that 60–80% of variation in the timing of pubertal onset is genetically determined. Self-limited delayed puberty (DP) segregates in an autosomal dominant pattern, but the underlying genetic background is unknown.Methods: We performed whole exome sequencing in 111 members of 18 families fro...