BIOL 120 - Study Guide - Test #4

Exam is scheduled for Monday, December 5th
Includes information from Chapters 8, 9, 13, 14, and 15

The exam with be entirely multiple choice, true/false, and matching. BRING A #2 PENCIL, ERASER, AND A NARROW SCANTRON SHEET. The following is a general outline of what I consider to be some of the more important points that we have covered so far. Test material will include everything covered through the end of Friday’s (Dec. 2nd) lecture.

CHAPTERS 8 & 9: Human Genetics (8: 10, 11; 9: 14, 15)

 

·         Humans and many other eukaryotes have two “kinds” of chromosomes: Autosomes (normal, everyday chromosomes); Sex chromosomes (those involved with determining sex)

·         In humans, it is the Y (or genes on the Y, specifically the SRYgene) that determines sex, the X has nothing to do with sex, but instead has normal, everyday genes

·         Sex Linkage: Genes located on the sex chromosomes are inherited in a criss-cross fashion. Y-linked genes are never expressed in females. X-linked recessive traits tend to be expressed more often in males than females. Males are said to be hemizygous for X-linked genes

·         X-chromosome Inactivation: in female mammals, one X chromosome in each cell is inactivated (called dosage compensation).  This X inactivation accounts for some differences between different tissues in some female mammals (i.e. calico coat color in cats).  Allows for both male and female cells to be the same with respect to X-linked genes

·         Human Disorders Caused by Changed in Chromosome Number

·         Nondisjunction = failure of chromosomes (or chromatids) to disjoin during meiosis.  1/2 of the gametes will have an extra chromosome, and 1/2 of the gametes will be missing a chromosome.  Results in aneuploidy.

·         Human Aneuploidy: Sex chromosome nondisjunction - know the following- Klinefelter syndrome, triplo-X, Turner syndrome, XXY.

·         Autosomal nondisjunction – know the following - Down syndrome, Edward syndrome, Patau syndrome.

·         Alterations of Chromosome Structure – Deletions, Duplications, Translocation, Inversion

·         Detection of chromosomal or genetic disorders: Amniocentesis, Chorionic villus sampling.

 

CHAPTERS 13 & 14: Classification, Speciation & Evolution (13:4; 14:1, 4, 5, 6, 7, 9, 12)

 

Chapter 15 – Geologic History & Macroevolution (15:3, 4, 5, 6, 10)