1. THE CHROMOSOMAL BASIS OF INHERITANCE

2. YOU MUST KNOW…
HOW THE CHROMOSOME THEORY OF INHERITANCE CONNECTS THE PHYSICAL MOVEMENT OF CHROMOSOMES IN MEIOSIS TO MENDEL’S LAWS OF INHERITANCE
THE UNIQUE PATTERN OF INHERITANCE IN SEX-LINKED GENES
HOW ALTERATION OF CHROMOSOME NUMBER OR STRUCTURALLY ALTERED CHROMOMES (DELETION, DUPLICATIONS, ETC.) CAN CAUSE GENETIC DISORDERS

3. CONCEPT 15.1
MENDELIAN INHERITANCE HAS ITS PHYSICAL BASIS IN THE BEHAVIOR OF CHROMOSOMES

4. CHROMOSOME THEORY OF INHERITANCE
STATES THAT GENES HAVE SPECIFIC LOCATIONS (LOCI) ON CHROMOSOMES AND THAT IT IS CHROMOSOMES THAT SEGREGATE AND
ASSORT
INDEPENDENTLY
SEX-LINKED GENE –
LOCATED ON A
SEX CHROMOSOME

5. CONCEPT 15.2
SEX-LINKED GENES EXHIBIT UNIQUE PATTERNS
OF INHERITANCE

6. SEX-LINKED GENES LOCATED ON THE X CHROMOSOME
SEX IS DETERMINED BY THE MALE SPERM CELL
FATHERS PASS SEX-LINKED GENES ON TO THEIR DAUGHTER BUT NOT TO THEIR SONS
FEMALES WILL EXPRESS A SEX-LINKED TRAIT LIKE ANY OTHER TRAIT BUT MALES WITH ONLY ONE X CHROMOSOME, WILL EXPRESS THE ALLELE ON THE X CHROMOSOME THEY INHERITED FROM THEIR MOTHER
THE VAST MAJORITY OF GENES ON THE X CHROMOSOME ARE NOT RELATED TO SEX

7. SEX-LINKED DISORDERS
DUCHENNE MUSCULAR DYSTROPHY – PROGRESSIVE WEAKING OF THE MUSCLES AND LOSS OF COORDINATION, RARELY LIVE PAST THEIR EARLY 20’S
HEMOPHILIA – BLOOD WITH AN INABILITY TO CLOT NORMALLY, CAUSED BY THE ABSENCE OF PROTEINS REQUIRED FOR BLOOD CLOTTING

9. X-INACTIVATION – REGULATES GENE DOSAGE IN FEMALES
ONE OF THE X CHROMOSOMES IN EACH CELL OF THE BODY BECOMES INACTIVATED DURING EMBRYONIC DEVELOPMENT BY METHYLATION
MALES AND FEMALES HAVE THE SAME EFFECTIVE DOSE OF GENES WITH LOCI ON THE X CHROMOSOME

10. THE INACTIVE CHROMOSOME CONDENSES INTO A BARR BODY WHICH LIES ALONG THE INSIDE OF THE NUCLEAR ENVELOPE
FEMALES ARE NOT AFFECTED AS HETEROZYGOTE CARRIERS OF PROBLEMATIC ALLELES BECAUSE HALF OF THEIR SEX CHROMOSOMES ARE NORMAL AND PRODUCE THE NECESSARY PROTEINS

11. CONCEPT 15.3
LINKED GENES TEND TO BE INHERITED TOGETHER BECAUSE THEY ARE LOCATED NEAR EACH OTHER ON THE SAME CHROMOSOME

12. LINKED GENES ARE LOCATED ON THE SAME CHROMOSOME AND THEREFORE TEND TO BE INHERITED TOGETHER DURING CELL DIVISION
GENETIC RECOMBINATION IS THE PRODUCTION OF OFFSPRING WITH A NEW COMBINATION OF GENES INHERITED FROM THE PARENTS
SAME PHENOTYPE AS ONE OF THE PARENTS (PARENT TYPES)
DIFFERENT PHENOTYPE THAN PARENTS (RECOMBINANTS)

13. CROSSING OVER – CAN EXPLAIN WHY SOME LINKED GENES GET SEPARATED DURING MEIOSIS
DURING MEIOSIS UNLINKED GENES FOLLOW INDEPENDENT ASSORTMENT BECAUSE THEY ARE LOCATED ON DIFFERENT CHROMOSOMES
LINKED GENES ARE LOCATED ON THE SAME CHROMOSOME AND WOULD NOT BE PREDICTED TO FOLLOW INDEPENDENT ASSORTMENT

15. LINKAGE MAP – GENETIC MAP THAT IS BASED ON THE % OF CROSS-OVER EVENTS
MAP UNIT – IS EQUAL TO A 1% RECOMBINATION FREQUENCY, USED TO EXPRESS RELATIVE DISTANCES ALONG THE CHROMOSOME

16. CONCEPT 15.4
ALTERATIONS OF CHROMOSOME NUMBER OR STRUCTURE CAUSE SOME GENETIC DISORDERS

17. NONDISJUNCTION
OCCURS WHEN THE MEMBERS OF A PAIR OF HOMOLOGOUS CHROMOSOMES DOES NOT SEPARATE PROPERLY
DURING MEIOSIS I OR
SISTER CHROMATIDS
DON’T SEPARATE
PROPERLY DURING
MEIOSIS II

18. ONE GAMETE RECEIVES TWO COPIES OF THE CHROMOSOME WHILE THE OTHER GAMETE RECEIVE NONE
IF THE FAULTY GAMETES ENGAGE IN FERTILIZATION, THE OFFSPRING WILL HAVE AN INCORRECT CHROMOSOME NUMBER KNOWN AS ANEUPLOIDY

19. TRISOMY – FERTILIZED EGG RECEIVES 3 COPIES OF THE CHROMOSOME (trisomy 21, 18, 13)
MONOSOMY – FERTILIZED EGG RECEIVES ONLY ONE COPY OF A CHROMOSOME

20. POLYPLOIDY – CONDITION OF HAVING MORE THAN TWO COMPLETE SETS OF CHROMOSOMES, FORMING A 3n OR 4n INDIVIDUAL

21. MUTATIONS
DELETION – WHEN A CHROMOSOMAL FRAGMENT IS LOST (MISSING GENES)
DUPLICATION – WHEN A CHROMOSOMAL FRAGMENT THAT BROKE OFF BECOMES ATTACHED TO ITS SISTER CHROMATID (ZYGOTE GETS A DOUBLE DOSE OF THE GENES)

23. MUTATIONS
INVERSION – WHEN A CHROMOSOME FRAGMENT BREAKS OFF AND REATTACHED TO ITS ORIGINAL POSITION BUT BACKWARD
TRANSLOCATION – WHEN A DELETED CHROMOSOME FRAGMENT JOINS A NONHOMOLOGOUS CHROMOSOME

25. DOWN SYNDROME – TRISOMY 21 – CHARACTERISTIC FACIAL FEATURES, SHORT STATURE, HEART DEFECTS, MENTAL RETARDATION
KLINEFELTER SYNDROME – XXY – HAVE MALE SEX ORGANS BUT ARE STERILE
TURNER SYNDROME – X – FEMALES ARE STERILE BECAUSE REPRODUCTIVE ORGANS DON’T MATURE