DOC PREVIEW
TAMU BIOL 111 - Exam 3 Study Guide
Type Study Guide
Pages 6

This preview shows page 1-2 out of 6 pages.

Save
View full document
View full document
Premium Document
Do you want full access? Go Premium and unlock all 6 pages.
Access to all documents
Download any document
Ad free experience
View full document
Premium Document
Do you want full access? Go Premium and unlock all 6 pages.
Access to all documents
Download any document
Ad free experience
Premium Document
Do you want full access? Go Premium and unlock all 6 pages.
Access to all documents
Download any document
Ad free experience

Unformatted text preview:

BIOL 111 1st EditionExam 3 Study Guide- Before Mendel (<1860s)—ideas about inheritanceo- Gregor Mendel (1822-1884): the Revolutionary monko Training in mathematicso Simple system-Pea plants: True breeding plants- Very prolific (get lots of offspring), grow very quickly, have lots of characteristics that are easy to follow- If you let the plant self-fertilize, the characteristics of the plant stay true Study one characteristic at a time- Mendel didn’t try to study everything at once and used different experimentsto study different characteristics Use quantitative analysis, determine patterns- Counting, measuring to get data- Experiment #1o Monohybrid cross: two true-breeding plants What traits appear in F1?- Purple and white flowers, the dominant trait is purple and the recessive is white Review:- P-the parents- F1-the offspring- True-breed- Hybrid- one of each of the traits from the true-breeding parents- Dominant-the trait that appears - Recessive –the trait that is covered up by the dominant traito Mendel’s simple system True breeding pea plants Study one characteristic at a time Count and determine patterns- Experiment #2 o What traits appear in F2?o Repeat with different characteristicso Notice ratio~3:1—Why? Realized that the blending hypothesis did not work anymore and decided to make a different modelo What is an allele (or heritable factor)? Like sister chromatids except that alleles are different from one another because one is from mom and one is from dad while sister chromatids are exactly identical to each other o Review  F2-second generation of species Allele-heritable factors that can be passed down form generation to generation - Meiosis oo Where are alleles during gamete formation? An individual trait has only one allele in gamete formation - How to geneticists represent alleles?o Dominant trait-CAPITAL lettero Recessive trait-lower case lettero Use letters to show all possible alleles present in gameteso Punnent square: used to predict possible offspring allele combos from parents with known genetic makeup - Law of segregation o Following one trait o Allele pairs separate (segregate) suring gametogenesis and re-pair at fertilizationo Review:  Homozygous-same alleles (AA, aa) Heterozygous-different alleles (Aa) Phenotype-the outward appearance of an individual (flower color purple) Genotype-the actual genetic make up of the individual (the alleles, AA)o F2 ratios: - Experiment #3: Test Crosso Determine unknown genotype of a dominant phenotype by crossing with recessive homozygote—why? If you did not cross with the homozygote, you would not know whether the unknown was homozygous or heterozygouso- Experiment #4: Dihybrid cross follow two traits for two generationso Now following two traits, start out with true breeding individuals and wants to find out if two traits are inherited independently/dependentlyo How to alleles segregate?  Independently or dependently?- Law of independent assortmento Determine possible gamete alleles for P generation RRYY, rryyo Predict genotype and phenotype of F1 Dependent assortment you would get YYRR, YyRr, YyRr yyrr and would get a phenotypic ratio of 3:1 Independent assortment you would get YYRR, YYRr, YyRR, YyRr, YYRr, YYrr, YyRr, Yyrr, YyRR, YyRr, yyRR, yyRr, YyRr, Yyrr, yyRr, yyrr and the phenotypic ratio is 9:3:3:1o Following two traits at a time=dihybrid crosso Each allele pair segregates independently of other pairs of alleles during gamete formation - Sex determination in mammals o Sex chromosomes—XY systemo Sex linked genes Examples in mammals- SRY gene-sex determining region of Y chromosomes- DAX gene-dosage sensitive gene on X chromosome- Sex-linked traits/disorderso Due to gene on a sex chromosome (X or Y)o Often recessive Female (XX)—carrier if heterozygous or affected by homozygous Male (XY)—hemizygous, affected if have gene- Ex. Color blindness, hemophiliao Sex-linked traits were one of the original pieces of evidence for genes associating with chromosomes- Discovery timelineo 1860s—Mendel’s laws of inheritanceo 1870-1890s—physical process of mitosis and meiosis discoveredo 1902—Sutton and Boveri propose chromosomal theory of inheritance (Medelian genes have specific loci/positions on chromosomes)- Thomas Hunt Morgan (early 1900’s)o Provided physical evidence for genes associating with chromosomeo Used Drosophilia melanogaster (Fig 15.3)o Studied sex-linked traits o Morgan’s correlation: a trait (eye-color) correlates with an individual’s sex lends support to chromosomal theory of inheritance- Genetic variation recombination of geneso Independent assortment recombines unlinked genes Examine figure 15.2—do all of the offspring look like the parents?o Independent assortment recombines unlinked genes Use TESTCROSS to study (figure 15.UN2 Pg. 294)o Crossing over recombines linked genes Figure 15.9—Morgan’s experiment #3 TESTCROSSo If TESTCROSS results in: Parental type—greater than 50% offspring phenotypes Recombinant type—much less than 50% offspring phenotypes new combos- THEN Linked genes: genes located on the same chromosome, “tend” to be inherited together but not always du to crossing over- Abnormal chromosome number o Nondisjunction-when homologous chromosomes or sister chromatids do NOT separate  Aneuploidy-offspring with abnormal number of a particular chromosome (monosomy, trisomy)- Ex. Down syndrome—trisomy 21, klinefelter syndrome (XXYY), turner syndrome (XO) Polyploidy-offspring with more than 2 complete chromosome sets- Triploidy (3N), tetraploid (4N), etc.- Testing for Genetic Disorderso Identify carriers-use in vitro fertilization and screen embryoso Fetal testing (Fig. 14-18)-amniocentesis, chorionic villus sampling, ultrasoundo Newborn screening-PKU (phenylketonuria)-treat with special


View Full Document

TAMU BIOL 111 - Exam 3 Study Guide

Type: Study Guide
Pages: 6
Documents in this Course
Water

Water

44 pages

Chapter 2

Chapter 2

26 pages

The Cell

The Cell

23 pages

Taxonomy

Taxonomy

45 pages

Notes

Notes

6 pages

Load more
Download Exam 3 Study Guide
Our administrator received your request to download this document. We will send you the file to your email shortly.
Loading Unlocking...
Login

Join to view Exam 3 Study Guide and access 3M+ class-specific study document.

or
We will never post anything without your permission.
Don't have an account?
Sign Up

Join to view Exam 3 Study Guide 2 2 and access 3M+ class-specific study document.

or

By creating an account you agree to our Privacy Policy and Terms Of Use

Already a member?