Lecture 11: Sex Determination and Differentiation Flashcards
Bipotential gonad
tissue has two potential pathways of development (testis or ovary)
Müllerian duct
develops into female reproductive tract
Wolffian duct
develops into male reproductive tract
5 a - reductase and SRY
enzyme that converts T to DHT. Only happens in a genotype that contains a functional SRY.
46, XX
normal human female
46, XY
normal human male
45, XO
Turner Syndrome - ovary develops, broad spectrum of phenotypes from spontaneous abortion (98% of pregnancies) to short stature, ovarian failure and infertility. Most require therapy to develop secondary sex characteristics.
47, XXY
Klinefelter Syndome - testis develops, decreased testicular hormonal function known as hypogonadism, low testosterone production, unable to make sperm, enlarged breasts/sparse facial hair/small testes
Y chromosome – SRY, AZF
Sex Determining Region on the Y Chromosome (SRY) sits on the short arm of the Y chromosome and determines male appearance.
AMH
Anti Mullerian Hormone, expressed by sertoli cells and leads to degeneration of the Mullerian duct (no oviduct, uterus, upper part of vagina). Only expressed in men with functional SRY.
DHT and SRY
converted from T by enzyme 5-a reductase. Again, only happens in man with functional SRY region.
Endocrine-disrupting compounds
chemicals in the environment that can mimic (agonistic) or obstruct (antagonistic) hormone function. Can target estrogens, androgens, or any other hormone system. Can affect sex determination.