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Chapter 5 Linkage, recombination, and the mapping of genes on chromosomes
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Fig. 5.1 linkage recombination
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w Y+ W+ y w Y+ W+ y w Y+ w Y+ w Y+ W+ y W+ Y+ wywy
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When genes are linked, parental combinations outnumber recombination types.
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W+ Y+ wywy W+ Y+ W+ Y+ wywy W+ Y+ Two parental types Two recombination types
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W+ Y+ wywy W+ Y+ W+ Y+ wywy W+ Y+
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Fig. 5.5 Autosomal genes can also exhibit linkage bb: blackcc: curved b c+ b c+ b+ c b c+ b+ c b+ c
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The Chi square test pinpoints the probability that experimental results are evident for linkage Chi test measures the “goodness of fit”: How often an experimentally observed deviation from the prediction of a particular hypothesis will occur solely by chance.
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Fig. 5.6 Assume A and B genes are not linked. F1
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Chi Square – Experiment 1 & 2 2 = (observed – expected) 2 number expected 2 = (31 – 25) 2 + (19 – 25) 2 2525 = 2.88 2 = (62 – 50) 2 + (38 – 50) 2 5050 = 5.76 Experiment 1 Experiment 2
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Table 5.1 A and B are not linked A and B are linked difference is significantdifference is non-significant
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Recombination results when crossing-over during meiosis separates linked genes
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Fig. 5.7 Evidence that recombination results from reciprocal exchange between homologous chromosomes X chromosome
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Fig. 5.8 Recombination through the light microscope (synaptonemal complex) anaphase
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Fig. 5.9 Recombination frequencies are the basis of genetic map RF: recombination frequency; 1% RF= 1 Centimorgan (cM)=1 map unit (m.u.)
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Fig. 5.10 Unlinked genes show a recombination frequency of 50% ry ry+ tkvtkv+ ry tkv ry tkv+ ry+ tkv ry+ tkv+
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Fig. 5.10 Unlinked genes show a recombination frequency of 50%
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Locus: chromosomal position of a gene Mapping: the process of determining that locus
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Fig. 5.11 Mapping genes by comparison of two-point crosses
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The limitation of two-point cross 1.Gene order is difficult to determine if they are very close. 2.Actually distance do not always add up.
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Fig. 5.12 Vestigial wings Black body Purple eye color
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Vg to b: (252+ 241+131+118)/4197=0.177, 17.7% Vg to pr: (252+241+13+9)/4197=0.123, 12.3% B to pr: (131+118+13+9)/4197=0.064, 6.4%
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Fig. 5.13 Three point-crosses allow correction for double cross-over
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Vg to b (three-point cross): (252+241+131+118+13+13+9+9)/4197=0.187, 18.7% Vg to b (two-point cross): (252+ 241+131+118)/4197=0.177, 17.7%
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For greatest accuracy, it is always best to construct a map using many genes separated by relative short distance.
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Mapping genes at X chromosome by two-point cross
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Fig. 5.14 RF between Y and W: 49+41+1+2/6823 X100=1.3 m.u. RF between m and W: 1203+1092+2+1/6823 X100=33.7 m.u RF between m and y: 1203+1029+49+41+2+2+1+1/6823 X100=35 m.u. y w m
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The actual physical distance between genes does not always show a direct correspondence to genetic map distance 1.Recombination is not uniform over the length of a single chromosome, Hot spot. The existence of double, triple, or even more cross-overs.
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Rates of recombination differ from species to species In human, 1 m.u. is = 1 million base In yeast, 1 m.u. is 1500 base pairs In Drosophila, meiotic recombination only occurs in female.
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Fig. 5.15 Linkage groups:
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Fig. 5.16a The life cycle of the yeast Saccharomyces cerevisiae stress
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Fig. 5.16b The life cycle of the bread mold Neurospora crassa Bread mold
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Fig. 5.17ab How meiosis can generate three kinds of tetrads
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Fig. 5.17cde When PD=NPD, two genes are unlinked
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Four types of gametes when genes on different chromosome H HHtt hhTT HthT H h h T T t t (h) (H)
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Fig. 5.18 When genes are linked, PDs exceed NPDs
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Fig. 5.19abc How crossovers between linked genes generate different tetrads
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Fig. 5.19def Rare!
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How to calculate the recombination frequency between two linked genes in the tetrad analyses? RF=(NPD+1/2 T)/total tetrads x100 RF= 3+(1/2)(70)/200 x100=19 m.u. (tetrads) = (4X3)+ (2X70)/800 x100=19 m.u. (spores)
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Fig. 5.20 Tetrad analyses confirms that recombination occurs at the four-strand stage (A mistake model!)(a lot)
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Fig. 5.22 How ordered tetrads form Arrangement of the four chromatids of each homologous chromosome pair
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Fig. 5.23 (Cross-over between gene and centromere) Ordered Tetrads help locate genes in relation to the centromere
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Fig. 5.24 Genetic mapping by ordered-tetrad analysis Thr-centromere: (1/2) (16+2+2+1)/105 x100=10 m.u. Arg-centromere:(1/2) (11+2+2+1)/105 x100=7.6 m.u.
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Thr-Arg linkage: 3+(1/2)(16+11+2)/105 X100=16.7 PD TTTNPD Double cross-over NPDTetrad Double cross-over Double cross-over Double cross-over
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Fig. 5.25 Mitotic recombination Wild-type tissue: y sn+/Y+ sn: wild-type color and bristle y sn+/y sn+Y+ sn /Y+ sny sn+/y sn+ Y+ sn /Y+ sn
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Fig. 5.26
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Fig. 5.27 Mitotic recombination during growth of diploid yeast colonies can create sectors ADE2/ade2 ade2/ade2 Recombinatioin betweem ade2 and centromere A A a a A A a a Mitotic recombination
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Fig. 5.28
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Fig. 5a.p131
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Fig. 5a.p143
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Fig. 5.21
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TABLES
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ART & PHOTOS
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CO 05
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