Molecular biology of the kisspeptin receptor: Signaling, function, and mutations

Suzy Drummond Carvalho Bianco, Ursula B. Kaiser

Research output: Chapter in Book/Report/Conference proceedingChapter

9 Scopus citations

Abstract

Kisspeptin receptor (KISS1R) signaling is essential for the hallmark increase in pulsatile GnRH secretion characteristic of the onset of puberty in humans and experimental animals. Loss-of-function mutations in KISS1R are associated with idiopathic hypogonadotropic hypogonadism in humans. Also, mutations with confirmed association with idiopathic central precocious puberty were identified in kisspeptin and KISS1R. These observations underscore the role of KISS1R signaling for normal pubertal development. Moreover, investigation of the mechanisms underlying the gain-of-function mutation in KISS1R indicates that the duration of KISS1R signaling is critical for the role of this receptor in timing the onset of puberty in humans. These findings further endorse the need to uncover the mechanisms, as well as yet-unknown proteins, involved in each step of KISS1R signaling. This knowledge is expected to advance our understanding of normal and abnormal pubertal development, as well as to help uncover the role of KISS1R signaling in nonhypothalamic tissues such as the placenta. This chapter discusses recent advances in the investigation of KISS1R signaling and function, as well as potential pathophysiological implications of naturally occurring mutations in this receptor identified in humans with reproductive disorders.

Original languageEnglish
Title of host publicationAdvances in Experimental Medicine and Biology
Pages133-158
Number of pages26
Volume784
DOIs
StatePublished - Dec 1 2013

Publication series

NameAdvances in Experimental Medicine and Biology
Volume784
ISSN (Print)00652598

ASJC Scopus subject areas

  • Biochemistry, Genetics and Molecular Biology(all)
  • Medicine(all)

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  • Cite this

    Bianco, S. D. C., & Kaiser, U. B. (2013). Molecular biology of the kisspeptin receptor: Signaling, function, and mutations. In Advances in Experimental Medicine and Biology (Vol. 784, pp. 133-158). (Advances in Experimental Medicine and Biology; Vol. 784). https://doi.org/10.1007/978-1-4614-6199-9-7