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Chapter 12 simplifies complex concepts in human genetics, focusing on chromosomes and inheritance. Humans possess 23 pairs of chromosomes, including sex chromosomes (XX in females and XY in males). The Y chromosome uniquely defines maleness and is passed down paternally. This chapter also covers X-linked genes, showcasing their higher prevalence in males. Key concepts include incomplete dominance, codominance, polygenic traits, multifactorial inheritance, and the effects of extra chromosomes, such as Down syndrome. Aimed at demystifying genetic principles, this version is perfect for learners.
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COMPLEX INHERITANCE Chapter 12- Simplified Version
CHROMOSOMES: • Humans have 23 pairs of chromosomes • One pair is sex chromosome: • XX in females, XY in males • It is the presence of Y chromosome that determines maleness.
Y CHROMOSOME • Does not have a homologous partner, and does not experience recombination during meiosis • Y chromosome a son inherits from his father is identical to Y chromosome his father inherited from his father (grandfather) • This can be used to establish paternity
X-LINKED GENES • Located on X chromosome • Disorders inherited on X chromosome are called X-linked disorders • More common in males than in females
INCOMPLETE DOMINANCE • EX: hair type • Heterozygotes have a phenotype intermediate between homozygous dominant and homozygous recessive
CODOMINANT TRAIT • EX: ABO blood type • Both maternal and paternal alleles contribute equally and separately to the phenotype
POLYGENIC TRAITS • Traits that are influenced by additive effects of multiple genes • Show a normal distribution in the population
MULTIFACTORIAL INHERITANCE • A persons phenotype is determined by both his or her genotype at a number of different genes as well as by environmental influence • EX: human height, cardiovascular disease, and depression
EXTRA CHROMOSOMES • Some genetic disorders result from having a chromosome number that differs from the usual 46 • EX: down syndrome (trisomy 21) has an extra copy of chromosome 21