Chapter 6: Problem 7
Why do human monosomics most often fail to survive prenatal development?
Chapter 6: Problem 7
Why do human monosomics most often fail to survive prenatal development?
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Get started for freeContrast the fertility of an allotetraploid with an autotriploid and an autotetraploid.
Human adult hemoglobin is a tetramer containing two alpha (a) and two beta ( \(\beta\) ) polypeptide chains. The \(\alpha\) gene cluster on chromosome 16 and the \(\beta\) gene cluster on chromosome 11 share amino acid similarities such that 61 of the amino acids of the \(\alpha\) -globin polypeptide ( 141 amino acids long) are shared in identical sequence with the \(\beta\) -globin polypeptide \((146\) amino acids long. How might one explain the existence of two polypeptides with partially shared function and structure on two different chromosomes? Include in your answer a link to Ohno's hypothesis regarding the origin of new genes during evolution.
Drosophila may be monosomic for chromosome \(4,\) yet remain fer tile. Contrast the \(\mathrm{F}_{1}\) and \(\mathrm{F}_{2}\) results of the following crosses involving the recessive chromosome 4 trait, bent bristles: (a) monosomic IV, bent bristles \(\times\) normal bristles; (b) monosomic \(\mathrm{IV}\), normal bristles \(\times\) bent bristles.
In a human genetic study, a family with five phenotypically normal children was investigated. Two children were "homozy. gous" for a Robertsonian translocation between chromosomes 19 and 20 (they contained two identical copies of the fused chromosome). They have only 44 chromosomes but a complete genetic complement. Three of the children were "heterozygous" for the translocation and contained 45 chromosomes, with one translocated chromosome plus a normal copy of both chromosomes 19 and \(20 .\) Two other pregnancies resulted in stillbirths. It was later discovered that the parents were first cousins. Based on this information, determine the chromosome compositions of the parents. What led to the stillbirths? Why was the discovery that the parents were first cousins a key piece of information in understanding the genetics of this family?
The primrose, Primula kewensis, has 36 chromosomes that are similar in appearance to the chromosomes in two related species, \(P .\) floribunda $(2 n=18)\( and \)P\(. verticillata \)(2 n=18) .$ How could P. kewensis arise from these species? How would you describe \(P\) kewensis in genetic terms?
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