CAMPBELL BIOLOGY V.2(BHCC>CUSTOM<)
CAMPBELL BIOLOGY V.2(BHCC>CUSTOM<)
18th Edition
ISBN: 9781323655573
Author: Urry
Publisher: PEARSON C
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Chapter 15.4, Problem 1CC
Summary Introduction

To determine: The reason for occurrence of Down syndrome in a child if chromosomal translocation occurs in gonads of the child’s parents, involving attachment of  third copy of chromosome 21 to chromosome 14.

Concept introduction:

Down syndrome is caused by chromosomal aberration in which trisomy of chromosome 21 occurs. The parents of the children with Down syndrome are normal.

Chromosomal translocation is a process in which a part of chromosome does not break during meiosis and is carried to the gamete as it is.

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Two phenotypically normal parents produce a phenotypically abnormal child in which chromosome 5 is missing part of its long arm but has a piece of chromosome 7 attached to it. The child also has one normal copy of chromosome 5 and two normal copies of chromosome 7.  With regard to chromosomes 5 and 7, what do you think are the chromosomal compositions of the parents?  Would it most likely be reciprocal translocation? It wouldn't be simple translocation because then the child would have the entirety of one chromosome and only some of the other, but in this case, there is only partial chromosome 5 and chromosome 7?
Approximately how many copies of chromosome 2 are found in a polytene chromosome in Drosophila?
About 5% of individuals with Down syndrome havea chromosomal translocation in which a third copy ofchromosome 21 is attached to chromosome 14. If thistranslocation occurred in a parent’s gonad, how could itlead to Down syndrome in a child?

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CAMPBELL BIOLOGY V.2(BHCC>CUSTOM<)

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