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Michael Cummings David Reisman University of South Carolina Development and Sex Determination Chapter 7

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7.1 The Human Reproductive System The human reproductive system We will not cover most of this information in this course because it is focused on anatomy rather than human genetics.

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Timing of Meiosis and Gamete Formation in Males and Females Males Spermatogenesis begins during puberty Millions of sperm are always in production Spermatogenesis takes about 48 days Each cell that undergoes meiosis produces 4 sperm Females Primary oocytes produced during embryonic development remain in meiosis I until ovulation Ovulation begins during puberty Meiotic division produces 1 large oocyte and 2-3 polar bodies

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The Largest Cell The human oocyte is the largest cell produced in the body. It is large enough to be seen with the naked eye

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Fig. 7-5a, p. 155

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7.2 From Fertilization to Birth Cell divisions in the zygote form an early embryonic stage called the blastocyst Blastocyst The developmental stage at which the embryo implants into the uterine wall Stem cells are derived from a blastocyst Inner cell mass A cluster of cells in the blastocyst that gives rise to the fetus

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Implantation Implantation The embryo implants in the uterine wall, and membranes develop to support the embryo Trophoblast Outer layer of cells in the blastocyst that gives rise to the membranes surrounding the embryo

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Embryonic Membranes and Placenta Chorion formed from trophoblast Releases human chorionic gonadotropin (hCG) hormone which maintains uterine lining and stimulates endometrial cells to produce hormoneshCG is what pregnancy tests detect Grows to eventually form the placenta

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Fig. 7-6a, p. 156 Fertilization Trophoblast (surface layer of cells of the blastocyst) Endometrium Implantation Endometrium Blastocoel Inner cell mass Uterine cavity Inner cell mass 21354

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Fig. 7-6b, p. 156 Start of amniotic cavity Start of embryonic disk Blood-filled spaces Chorionic villi Chorionic cavity Chorion Amniotic cavity Connective tissue Start of yolk sac Start of chorionic cavity Yolk sac Actual size 6 8 7

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Development is Divided into Three Trimesters First trimester First month: basic tissue layers form; most of the body is divided into paired segments Second month: most major organ systems are formed Third month: embryo becomes a fetus; sexual development is initiated

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Development is Divided into Three Trimesters Second trimester Increase in size and organ-system development Bony parts of skeleton form Heartbeat is heard with a stethoscope Fetal movements begin Third trimester Rapid growth Circulatory and respiratory systems mature Birth is a hormonally induced process at the end of the 3rd trimester

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WEEKS 56 Head growth exceeds growth of other regions Retinal pigment Future external ear Upper-limb differentiation (hand plates develop, then digital rays of future fingers; wrist, elbow start forming) Umbilical-cord formation between weeks 4 and 8 (amnion expands, forms tube that encloses the connecting stalk and a duct for blood vessels) Foot plate (b) Actual length Fig. 7-7ab, p. 158

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WEEK 8 Final week of embryonic period; embryo looks distinctly human compared to other vertebrate embryos Upper and lower limbs well formed; fingers and then toes have separated Primordial tissues of all internal, external structures now developed Tail has become stubby (c) Actual length Fig. 7-7cd, p. 159

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Placenta WEEK 16 Length: 16 centimeters (6.4 inches) 200 grams (7 ounces) Weight: WEEK 29 Length: 27.5 centimeters (11 inches) 1,300 grams (46 ounces) Weight: WEEK 38 (full term) Length: 50 centimeters (20 inches) 3,400 grams (7.5 pounds) Weight: During fetal period, length measurement extends from crown to heel (for embryos, it is the longest measurable dimension, as from crown to rump). (d)

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7.3 Teratogens Are a Risk to the Developing Fetus Teratogen Any physical or chemical agent with the potential to cause birth defects Radiation, viruses, medications, alcohol

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Alcohol is a Teratogen Fetal alcohol syndrome (FAS) A range of birth defects caused by maternal alcohol consumption during pregnancy Alcohol is the most common teratogenic problem and leading cause of preventable birth defects There is no safe amount of alcohol consumption during pregnancy

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Fig. 7-8, p. 160 Defects in physiology; physical abnormalities minor Major morphological abnormalities Weeks: 12345678916203638 Cleavage, implantation Future heart Future eye Future ear Palate forming Limb buds Teeth External genitalia Central nervous system Heart Upper limbs Eyes Lower limbs Teeth Palate External genitalia Insensitivity to teratogens Ear Future brain Tetatogens and their impact on organ formation

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Mechanisms of Sex Determination Mechanisms of sex determination vary from species to species XX/XY system XX/X0 ZW/ZZ Temp.

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Human Sex Ratios Sex ratio The proportion of males to females changes throughout the life cycle The ratio at conception is slightly higher for males. (**prenatal deaths most likely due to lethal X-linked recessive alleles) The ratio at birth is about 105 males/100 females The ratio of females to males increases as a population ages

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Sexual Development begins in the Seventh week of Gestation

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7.5 Defining Sex in Stages: Chromosomes, Gonads, and Hormones Sex of an individual is defined at three levels Chromosomal sex (established at fertilization) Gonadal sex (begins around week 7 or 8 of embryogenesis) Phenotypic sex Gonadal and phenotypic sex depend on the interaction of genes and environmental factors, especially hormones

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Gonadal Sex Differentiation For the fist 7 or 8 weeks, the embryo is neither male nor female Both male and female reproductive duct systems begin to develop Genes cause gonads to develop as testes or ovaries, establishing gonadal sex Alternative pathways produce an intermediate sex for 1 out of every 2000 births.

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Y Chromosome and Testis Development SRY gene Sex-determining region of the Y chromosome Plays a major role in causing the undifferentiated gonad to develop into a testis Testis development causes secretion of testosterone Mllerian inhibiting hormone (MIH) Hormone produced by developing testis that causes breakdown of Mllerian (female) ducts in the embryo

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Female Development Requires the absence of the Y chromosome and the presence of two X chromosomes for the embryonic gonad to develop as an ovary In the absence of testosterone, the Wolffian duct system degenerates In the absence of MIH, the Mllerian duct system forms female reproductive system

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Fig. 7-14, p. 167 Egg with X sex chromosome MaleFemale Fertilized by Sperm with Y chromosome Sperm with X chromosome Embryo with XY sex chromosomes Chromosomal sex Embryo with XX sex chromosomes Sex-determining region of the Y chromosome (SRY) brings about development of undifferentiated gonads into testes. No Y chromosome, so no SRY. With no masculinizing inuence, undifferentiated gonads develop into ovaries. Gonadal sex Testes secrete masculinizing hormones, including testosterone, a potent androgen. No androgens secreted In presence of testicular hormones, undifferentiated reproductive tract and external genitalia develop along male lines. With no masculinizing hormones, undifferentiated reproductive tract and external genitalia develop along female lines. Phenotypic sex

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Androgen Insensitivity Androgen insensitivity (CAIS) A mutation in the X-linked androgen receptor gene (AR) causes XY males to become phenotypic females Testosterone is produced, but not testosterone receptors; cells develop as females

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XY Female with Androgen Insensitivity Fig. 7-15, p. 168

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Exploring Genetics: Joan of Arc or John of Arc? Joan of Arc fought with the French at the Battle of Orleans, and was burned as a heretic by her enemies, the English, in 1431 From an examination of trial evidence and records of her physical examinations, R.B. Greenblatt proposed that Joan had phenotypic characteristics of androgen insensitivity

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Mutations can cause Sex Phenotypes to Change at Puberty Pseudohermaphroditism Mutations in several different genes cause XY individuals to develop the phenotype of females Affected individuals have structures that appear female at birth At puberty, testosterone burst causes a change into the male phenotype

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7.7 Equalizing the Expression of X Chromosomes in Males and Females Lyon hypothesis (proposed by Mary Lyon) How do females avoid getting a double dose of protein from X-linked genes? Random inactivation of one X chromosome in females equalizes the activity of X-linked genes Barr body A densely staining mass in the somatic nuclei of mammalian females An inactivated X chromosome, tightly coiled

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X Chromosomes and Barr Bodies Fig. 7-16, p. 169

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Female Mammals are Mosaics for X Chromosome Expression In females, some cells express the mothers X chromosome and some cells express the fathers X chromosome Inactivated chromosome can come from either mother or father Inactivation occurs early in development Inactivation is permanent; all descendants of a particular cell have the same X inactivated

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Female Mammals are Actually Mosaics for X Chromosome Expression

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Fig. 7-18, p. 171 Unaffected skin (X chromosome with recessive allele was condensed; its allele is inactivated. The dominant allele on other X chromosome is being expressed in this tissue.) Affected skin with no normal sweat glands (yellow). In this tissue, the X chromosome with dominant allele has been condensed. The recessive allele on the other X chromosome is being transcribed. (a) (b) Female Mammals are Mosaics for X Chromosome Expression

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Mosaic Expression in Female Mammals Fig. 7-17, p. 170 The gene for fur color in cats is on the X chromosome.

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Inactivation of X Chromosome by XIST RNA Fig. 7-19, p. 171 XIST gene codes for RNA that binds to the X chromosome and inactivates it

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7.8 Sex-Related Phenotypic Effects Sex-limited trait - affects a structure or function of the body that is present in only males or females Women do not get prostate cancer, women do not grow beards but pass on the gene for beard growth on to their sons Sex-influenced trait - an allele is dominant in one sex and recessive in the other Baldnessthe allele is dominant in males and recessive in females

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Imprinting Imprinting difference in expression of a gene depending upon whether it was inherited from mother or father More discussion to follow on this topic in Chapter 11.