Sexual differentiation in humans

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The Human Y Chromosome showing the SRY gene which codes for a protein regulating sexual differentiation.

Sexual differentiation in humans is the process of development of sex differences in humans. It is defined as the development of phenotypic structures consequent to the action of hormones produced following gonadal determination.[1] Sexual differentiation includes development of different genitalia and the internal genital tracts, breasts, body hair, and plays a role in gender identification.[2]

The development of sexual differences begins with the XY sex-determination system that is present in humans, and complex mechanisms are responsible for the development of the phenotypic differences between male and female humans from an undifferentiated zygote.[3] Females have two X chromosomes, and males have a Y chromosome and an X chromosome. At an early stage in embryonic development, both genders possess equivalent internal structures. These are the mesonephric ducts and paramesonephric ducts. The presence of the SRY gene on the Y chromosome causes the development of the testes in males, and the subsequent release of hormones which cause the paramesonephric ducts to regress. In females, the mesonephric ducts regress.

Abnormal sexual development, and ambiguous genitalia, can be a result of genetic and hormonal factors.[4]

Sex determination[edit]

A baby’s sex is determined at the time of conception. When the baby is conceived, a chromosome from the sperm cell, either X or Y, fuses with the X chromosome in the egg cell, determining whether the baby will be genetically female (XX) or male (XY).[5] To be genetically female, one needs to be (XX), whereas to be a genetic male, (XY) is needed. It is the Y chromosome that is essential for the development of the male reproductive organs, and with no Y chromosome, an embryo will develop into a female. This is because of the presence of the sex determining region of the Y chromosome, also known as the SRY gene.[6]

A fetus doesn't develop its external sexual organs until -the fourth month of pregnancy —seven weeks after conception. The fetus appears to be sexually indifferent, looking neither like a male or a female. Over the next five weeks, the fetus begins producing hormones that cause its sex organs to grow into either male or female organs. This process is called sexual differentiation. The precursor of the internal female sex organs is called the Müllerian system.

Reproductive system[edit]

Differentiation between the sexes of the sex organs occurs throughout embryological, fetal and later life. This includes both internal and external genital differentiation. In both males and females, the sex organs consist of three structures: the gonads, the internal genitalia, and the external genitalia. In males, the gonads are the testes and in females they are the ovaries. These are the organs that produce gametes (egg and sperm), the reproductive cells that will eventually meet to form the fertilized egg (zygote).

As the zygote divides, it first becomes the embryo, typically between zero to eight weeks, then from the eighth week until birth, it is considered the fetus. The internal genitalia are all the accessory glands and ducts that connect the gonads to the outside environment. The external genitalia consist of all the external reproductive structures. The sex of an early embryo cannot be determined because the reproductive structures do not differentiate until the seventh week. Prior to this, the tissue is considered bipotential because it cannot be identified as male or female.

Internal genital differentiation[edit]

The internal genitalia consist of two accessory ducts: mesonephric ducts (male) and paramesonephric ducts (female). The mesonephric system is the precursor to the male genitalia and the paramesonephric to the female reproductive system.[7] As development proceeds, one of the pairs of ducts develops while the other regresses. This depends on the presence or absence of the sex determining region of the Y chromosome, also known as the SRY gene.[6] In the presence of a functional SRY gene, the bipotential gonads develop into testes. Gonads are histologically distinguishable by 6–8 weeks of gestation.

Subsequent development of one set and degeneration of the other depends on the presence or absence of two testicular hormones: testosterone and anti-müllerian hormone (AMH). Disruption of typical development may result in the development of both, or neither, duct system, which may produce morphologically intersexual individuals.

Males: The SRY gene when transcribed and processed produces SRY protein that binds to DNA and directs the development of the gonad into testes. Male development can only occur when the fetal testis secretes key hormones at a critical period in early gestation. The testes begin to secrete three hormones that influence the male internal and external genitalia: they secrete anti-müllerian hormone (AMH), testosterone, and dihydrotestosterone (DHT). Anti-müllerian hormone causes the paramesonephric ducts to regress. Testosterone converts the mesonephric ducts into male accessory structures, including the epididymis, vas deferens, and seminal vesicle. Testosterone will also control the descending of the testes from the abdomen into the scrotum.[1] Many other genes found on other autosomes, includingWT-1, SOX9, SF-1 also play a role in gonadal development.[5]

Females: Without testosterone and AMH, the mesonephric ducts degenerate and disappear. The paramesonephric ducts develop into a uterus, fallopian tubes, and upper vagina.[5]

External genital differentiation[edit]

Alternative text

By 7 weeks, a fetus has a genital tubercle, urogenital groove and sinus, and labioscrotal folds. In females, without excess androgens, these become the clitoris, urethra and vagina, and labia.

Males become externally distinct between 8 and 12 weeks, as androgens enlarge the phallus and cause the urogenital groove and sinus to fuse in the midline, producing an unambiguous penis with a phallic urethra, and a thinned, rugated scrotum. Dihydrotestosterone will differentiate the remaining male characteristics of the external genitalia.[1]

A sufficient amount of any androgen can cause external masculinization. The most potent is dihydrotestosterone (DHT), generated from testosterone in skin and genital tissue by the action of 5α-reductase. A male fetus may be incompletely masculinized if this enzyme is deficient. In some diseases and circumstances, other androgens may be present in high enough concentrations to cause partial or (rarely) complete masculinization of the external genitalia of a genetically female fetus. The testes begin to secrete three hormones that influence the male internal and external genitalia. They secrete anti-müllerian hormone, testosterone, and Dihydrotestosterone. anti-Müllerian hormone (AMH) causes the paramesonephric ducts to regress. Testosterone, which is secreted and converts the mesonephric ducts into male accessory structures, such as epididymis, vas deferens and seminal vesicle. Testosterone will also control the descending of the testes from the abdomen into the scrotom. Dihydrotestosterone, also known as (DHT) will differentiate the remaining male characteristics of the external genitalia.[9]

Further sex differentiation of the external genitalia occurs at puberty, when androgen levels again become disparate. Male levels of testosterone directly induce growth of the penis, and indirectly (via DHT) the prostate.

Alfred Jost observed that while testosterone was required for mesonephric duct development, the regression of the paramesonephric duct was due to another substance. This was later determined to be paramesonephric inhibiting substance (MIS), a 140 kD dimeric glycoprotein that is produced by sertoli cells. MIS blocks the development of paramesonephric ducts, promoting their regression.[10]

Defeminization and masculinization[edit]

Defeminization and masculinization are the differentiating processes that a fetus goes through to become male. Although, it may seem that this would make the female brain the “default” brain, this is not necessarily the case. Female brains still use hormones, such as estradiol, to undergo differentiation.[11]

Biologically, this perspective is supported by the fact that there are neither female genes nor female hormones that correspond to the hormones active in males only. Estrogen, for instance, is present in both the male and female fetus.

Secondary sexual characteristics[edit]

Breast[edit]

Visible differentiation occurs at puberty, when estradiol and other hormones cause breasts to develop in girls. However, fetal or neonatal androgens may modulate later breast development by reducing the capacity of breast tissue to respond to later estrogen.[citation needed]

Psychological and behavioral differentiation[edit]

Human adults and children show many psychological and behavioral sex differences, both dichotomous and dimorphic. Some (e.g., dress) are learned and obviously cultural. Others are demonstrable across cultures and may have both biological and learned determinants. For example, girls are, on average, more verbally fluent than boys, but boys are, on average, better at spatial calculation.[12][13] Because people cannot explore hormonal influences on human behavior experimentally, the relative contributions of biological factors and learning to human psychological and behavioral sex differences (especially gender identity, role, and sexual orientation) remain unsettled and controversial.

Current theories of mechanisms of sexual differentiation of brain and behaviors in humans are based primarily on three sources of evidence: animal research involving manipulation of hormones in early life, observation of outcomes of small numbers of individuals with disorders of sexual development (intersex conditions or cases of early sex reassignment), and statistical distribution of traits in populations (e.g., rates of homosexuality in twins). Many of these cases suggest some genetic or hormonal effect on sex differentiation of behavior and mental traits.[14]

In addition to affecting development, changing hormone levels affect certain behaviors or traits that are gender dimorphic, such as superior verbal fluency among women.[15]

Biology of gender[edit]

Main article: Biology of gender

Biology of gender is the scientific analysis of the physical basis for behavioural differences between men and women. It deals with gender identity, gender roles and sexual orientation.

Pathologies[edit]

The following disorders are caused by a malfunction in the sex determination and differentiation process:[16]

  • A zygote with only X chromosome (XO) results in Turner’s syndrome and will develop with female characteristics.[6]
  • Congenital adrenal hyperplasia - Inability of adrenal to produce sufficient cortisol, leading to increased production of testosterone resulting in severe masculinization of 46 XX females.
  • Persistent müllerian duct syndrome - A rare type of pseudohermaphroditism that occurs in 46 XY males, caused by either a mutation in the Müllerian inhibiting substance (MIS) gene, on 19p13, or its type II receptor, 12q13. Results in a retention of Müllerian ducts (persistence of rudimentary uterus and fallopian tubes in otherwise normally virilized males), unilateral or bilateral undescended testes and sometimes causes infertility.
  • Male pseudohermaphroditism - Failure of androgen production or inadequate androgen response, which can cause incomplete masculinization in XY males. Varies from mild failure of masculinization with undescended testes to complete sex reversal and female phenotype (Androgen insensitivity syndrome)
  • Swyer syndrome. A form of complete gonadal dysgenesis, mostly due to mutations in the first step of sex determination; the SRY genes.
  • A 5-alpha reductase deficiency results in an androgen disorder characterized by female phenotype or severely undervirilized male phenotype with development of the epididymis, vas deferens, seminal vesicle, and ejaculatory duct, but also a pseudovagina. This is because testosterone is converted to the more potent DHT by 5-alpha reductase. DHT is necessary to exert androgenic effects farther from the site of testosterone production, where the concentrations of testosterone are too low to have any potency.

Timeline[edit]

Human prenatal sexual differentiation[17]
Fetal age
(weeks)
Crown-rump length
(mm)
Sex differentiating events
0 blastocyst Inactivation of one X chromosome
4 2-3 Development of wolffian ducts
5 7 Migration of primordial germ cells in the undifferentiated gonad
6 10-15 Development of müllerian ducts
7 13-20 Differentiation of seminiferous tubules
8 30 Regression of müllerian ducts in male fetus
8 32-35 Appearance of Leydig cells. First synthesis of testosterone
9 43 Total regression of müllerian ducts. Loss of sensitivity of müllerian ducts in the female fetus
9 43 First meiotic prophase in oogonia
10 43-45 Beginning of masculinization of external genitalia
10 50 Beginning of regression of wolffian ducts in the female fetus
12 70 Fetal testis is in the internal inguinal ring
12-14 70-90 Male penile urethra is completed
14 90 Appearance of first spermatogonia
16 100 Appearance of first ovarian follicles
17 120 Numerous Leydig cells. Peak of testosterone secretion
20 150 Regression of Leydig cells. Diminished testosterone secretion
24 200 First multilayered ovarian follicles. Canalisation of the vagina
28 230 Cessation of oogonia multiplication
28 230 Descent of testis

References[edit]

  1. ^ a b c Hughes, Ieuan A. . (June 12, 2011). Minireview: Sex Differentiation. Available: http://endo.endojournals.org/content/142/8/3281.full. Last accessed May 21, 2011.
  2. ^ http://www.gfmer.ch/Books/Reproductive_health/Human_sexual_differentiation.html[full citation needed]
  3. ^ Mukherjee, Asit B.; Parsa, Nasser Z. (1990). "Determination of sex chromosomal constitution and chromosomal origin of drumsticks, drumstick-like structures, and other nuclear bodies in human blood cells at interphase by fluorescence in situ hybridization". Chromosoma 99 (6): 432–5. doi:10.1007/BF01726695. PMID 2176962. 
  4. ^ Kučinskas, Laimutis; Just, Walter (2005). "Human male sex determination and sexual differentiation: Pathways, molecular interactions and genetic disorders". Medicina 41 (8): 633–40. PMID 16160410. 
  5. ^ a b c Harrison's principles of internal medicine. (17th ed. ed.). New York [etc.]: McGraw-Hill Medical. 2008. pp. 2339–2346. ISBN 978-0-07-147693-5. 
  6. ^ a b c Rey,Rodolfo, MD, PhD, Josso, Nathalie MD, PhD. (). Chapter 7. Sexual Differentiation. Available: http://www.endotext.org/pediatrics/pediatrics7/pediatrics7.html. Last accessed may 21, 2011.
  7. ^ http://www.albany.edu/faculty/cafrye/apsy601/Ch.09Sex.html
  8. ^ Silverthorn, Dee, U.. (2010). Reproduction and Development. In: Human Physiology: an integrated approach. 5th ed. san francisco: Pearson education. p828-831.
  9. ^ Hughes, Ieuan A. . (June 12, 2011).
  10. ^ Jost, A.; Price, D.; Edwards, R. G. (1970). "Hormonal Factors in the Sex Differentiation of the Mammalian Foetus [and Discussion]". Philosophical Transactions of the Royal Society B: Biological Sciences 259 (828): 119–31. doi:10.1098/rstb.1970.0052. JSTOR 2417046. 
  11. ^ Dohler KD, Hancke JL, Srivastava SS, Hofmann C, Shryne JE, Gorski RA. Participation of estrogens in female sexual differentiation of the brain; neuroanatomical, neuroendocrine and behavioral evidence. Prog Brain Res 1984; 61: 99–117.
  12. ^ Halpern, Diane F. (2011). Sex Differences in Cognitive Abilities: 4th Edition. NY: Psychology Press.
  13. ^ Geary, David C. (2009). Male, Female: The Evolution of Human Sex Differences (2nd Ed.) Washington, D.C.: American Psychological Association.
  14. ^ Pinker, Steven (2002). The Blank Slate. New York: Penguin. pp. 346–350. 
  15. ^ Pinker, Steven (2002). The Blank Slate. New York: Penguin. pp. 347–348. 
  16. ^ MacLaughlin, David T.; Donahoe, Patricia K. (2004). "Sex Determination and Differentiation". New England Journal of Medicine 350 (4): 367–78. doi:10.1056/NEJMra022784. PMID 14736929. 
  17. ^ PC Sizonenko in Pediatric Endocrinology, edited by J. Bertrand, R. Rappaport, and PC Sizonenko, (Baltimore: Williams & Wilkins, 1993), pp. 88–99

Further reading[edit]

  • Andy. (January 16, 2011). Sex determination and differentiation. AmericanTransMan. June 26, 2012. [1]
  • Marshall Graves, Jennifer A. (2000). "Human Y Chromosome, Sex Determination, and Spermatogenesis—A Feminist View". Biology of Reproduction 63 (3): 667–76. doi:10.1095/biolreprod63.3.667b (inactive October 31, 2012). PMID 10952906. 
  • Josso, Nathalie. (May 10, 2008). Sex Determination. Differences of Sex Determination. June 26, 2012. [2]
  • De Felici, M. (2010). "Germ stem cells in the mammalian adult ovary: Considerations by a fan of the primordial germ cells". Molecular Human Reproduction 16 (9): 632–6. doi:10.1093/molehr/gaq006. PMID 20086005. 
  • Rodolfo Rey. (November 10, 2009). Externalgenitalia. Endotext. June 26, 2012. [3]
  • Sharman, GB; Hughes, RL; Cooper, DW (1989). "The Chromosomal Basis of Sex-Differentiation in Marsupials". Australian Journal of Zoology 37 (3): 451. doi:10.1071/ZO9890451. 
  • Watson, CM; Margan, SH; Johnston, PG (1998). "Sex-chromosome elimination in the bandicoot Isoodon macrourus using Y-linked markers". Cytogenetics and cell genetics 81 (1): 54–9. doi:10.1159/000015008. PMID 9691176. 
  • Minireview: Sex Differentiation. Available: http://endo.endojournals.org/content/142/8/3281.full. Last accessed May 21, 2011.