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BIOLOGY 12 CHROMOSOMAL MUTATIONS referenced Horton High E-Biology Chromosomal Mutations changes in chromosomal number changes in chromosomal structure Chromosomal Number monosomy occurs when and individual has only one of a particular type of chromosome trisomy occurs when and individual has three of a particular type of chromosome monosomy and trisomy occur in plants and animals generally lethal in the body cells of animals nonlethal human monosomies and trisomies include the following: Turner syndrome: monosomy where the individual has single X chromosome Down syndrome is most common trisomy among humans; it involves chromosome 21 Chromosomal Number cont. nondisjunction is the failure of chromosomes to separate it is more common during meiosis I than meiosis II it can occur in mitosis polyploidy: offspring end up with more than two complete sets of chromosomes polyploidy does not increase variation in animals, would likely be lethal polyploidy is a major evolutionary mechanism in plants successful polyploidy results in a new species Chromosomal Structure Disorders Down syndrome most common autosomal trisomy, involves chromosome 21 Down syndrome child has tendency for leukemia, cataracts, faster aging, and mental retardation Turner (XO) syndrome females have only one sex chromosome, an X Turner females are short, have broad chest and webbed neck ovaries of Turner females never become functional; therefore, do not undergo puberty Klinefelter syndrome males have one Y chromosome and two or more X chromosomes affected individuals are sterile males; testes and prostate are underdeveloped individuals have large hands and feet and long arms and legs Disorders cont. Triplo-X females have three or more X chromosomes there is no increased femininity; most lack any physical abnormalities there is an increased risk of having triplo-X daughters of XXY sons may experience menstrual irregularities, including early onset of menopause XYY males with Jacob syndrome have two Y chromosomes instead of one results from nondisjunction during meiosis II usually taller than average; suffer from persistent acne; tend to have lower intelligence earlier claims that XYY individuals were likely to be aggressive are not correct Disorders cont. Fragile X Syndrome X chromosome is nearly broken; most often found in males as children: hyperactive or autistic; delayed speech; account for part of higher proportion of males in institutions for mentally retardation as adults: large testes, unusually protruding ears occurs in females, but symptoms are less severe