exam 1 Flashcards
preformation/uniparental inheritance vs blended inheritance
preformation/ uniparental inhertiance: traits determined by just one parent (female for “ovists”, male for “spermists”)
blended inheritance: offspring merge information from both parents, resulting in a unique blend
prevalent views of inheritance before Mendel
- problem was they lacked explanatory or predictive power
walther flemming
- discovered mitosis: “process of threads”
- looked at live salamander tail fin cells
- dyed cells inside nucleus stained vigorously
- called it chromatin
Theodor Boveri (1895) and E.B. Wilson (1896)
found that there was something special about the nucleus
- removed nuclei from sea urchin eggs and replaced them with transplanted nuclei
- never grew to adulthood but sometimes eggs with transplanted nuclei were able to hatch into larvae!
- suggests that something in the nuclei (chromosomes) are required for creating an organism
eukaryotic chromosomes
are a nucleoprotein complex
- eukaryotic chromosomes have linear DNA molecules associated with large amount of protein
- DNA wrapped around histone proteins
- wrapping and unwrapping is highly regulated
chromatin
chromatin, complex of DNA and protein, is found in the nucleus of eukaryotic cells
- during cell division, chromatin condenses to form structures seen by Flemming (not easily visible during interphase, easily visible during mitosis)
5 phases of mitosis
Prophase: chromosomes starting to condense, spindle forming
Prometaphase: chromosomes condensed, nuclear envelope breakdown
Metaphase: chromosomes meet at the middle
Anaphase: chromosomes move apart
Telophase: cells start dividing; cytokinesis (separation of 2 daughter cells)
Walter sutton (1903)
- discovered that chromosomes come in pairs
- via meiosis in gonads, each gametes gets a single member of a chromosome pair: eggs and sperm have half the regular number of chromosomes
- surmised that during fertilization, the egg and sperm each contribute a member of a chromosome pair, regenerating the full number of chromosomes
2 sets of cell divisions in meiosis
meiosis I: separation of homologous chromosomes
meiosis II: separation of sister chromatids
- 2 cell divisions result in 4 daughter cells rather than 2 daughter cells in mitosis
- each daughter cell has only half as many chromosomes as the parent cell
nattie stevens (1905)
- used drosophila (fruit flies)
- died of breast cancer early though
- discovered that males have the Y and females have the XX
T.H. Morgan (1910)
- discovered sex linkage after discovering and mating the white-eyed male
- concluded that Mendel’s genes reside physically on chromosomes (on the X chromosome)
carrier
someone who carries one of the diseased alleles but themselves is not affected
Alfred sturtevant +recombinant frequency
stared at Morgan (white eye cross guy)’s data and said that recombinant frequencies are a measure of the physical distance between genes on a chromosome
- mapped distance between genes on chromosomes
recombinant frequency = distance b/w genes
chiasmata
X-shaped regions where crossing over occurs
- each tetrad usually has 1 or more chiasmata
tetrad: each pair of chromosomes forms a tetrad, a group of 4 chromatids
when do homologous chromosomes cross over
in prophase I
crossing over: non sister chromatids exchange DNA segments
importance of sexual reproduction + 3 important contributing factors
creates genetic variation because of:
- independent assortment of chromosomes
- random fertilization
- crossing over (recombination)