Which of the following chromosomal mutations increases the amount of genetic material from only some chromosomes?
Table of contents
- 1. Introduction to Genetics51m
- 2. Mendel's Laws of Inheritance3h 37m
- 3. Extensions to Mendelian Inheritance2h 41m
- 4. Genetic Mapping and Linkage2h 28m
- 5. Genetics of Bacteria and Viruses1h 21m
- 6. Chromosomal Variation1h 48m
- 7. DNA and Chromosome Structure56m
- 8. DNA Replication1h 10m
- 9. Mitosis and Meiosis1h 34m
- 10. Transcription1h 0m
- 11. Translation58m
- 12. Gene Regulation in Prokaryotes1h 19m
- 13. Gene Regulation in Eukaryotes44m
- 14. Genetic Control of Development44m
- 15. Genomes and Genomics1h 50m
- 16. Transposable Elements47m
- 17. Mutation, Repair, and Recombination1h 6m
- 18. Molecular Genetic Tools19m
- 19. Cancer Genetics29m
- 20. Quantitative Genetics1h 26m
- 21. Population Genetics50m
- 22. Evolutionary Genetics29m
6. Chromosomal Variation
Chromosomal Mutations: Aneuploidy
Problem 1b
Textbook Question
How do we know that human aneuploidy for each of the 22 autosomes occurs at conception, even though most often human aneuploids do not survive embryonic or fetal development and thus are never observed at birth?
Verified step by step guidance1
Understand the definition of aneuploidy: it is the presence of an abnormal number of chromosomes in a cell, such as having an extra or missing chromosome.
Recognize that although many aneuploid embryos do not survive to birth, scientists can detect aneuploidy at very early stages of development, such as at conception or shortly after fertilization.
Learn about techniques like preimplantation genetic diagnosis (PGD) and fluorescence in situ hybridization (FISH), which allow researchers to analyze the chromosome number in single cells from early embryos before implantation.
Consider cytogenetic studies of miscarried embryos and fetuses, which reveal the presence of aneuploidy in many cases, indicating that aneuploidy occurs early but often leads to developmental failure.
Combine evidence from early embryo testing and studies of spontaneous abortions to conclude that aneuploidy for all 22 autosomes arises at conception, even if most affected embryos do not survive to birth.
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Key Concepts
Here are the essential concepts you must grasp in order to answer the question correctly.
Aneuploidy and Its Definition
Aneuploidy refers to the presence of an abnormal number of chromosomes in a cell, such as having an extra or missing chromosome. In humans, this often involves one of the 22 autosomes and can disrupt normal development. Understanding aneuploidy is essential to grasp why some embryos fail to develop properly.
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Detection of Aneuploidy at Conception
Techniques like preimplantation genetic diagnosis (PGD) and analysis of products of conception allow detection of aneuploidy very early, often at or shortly after fertilization. These methods reveal that aneuploid embryos are formed frequently, even if they do not survive to birth, providing evidence of aneuploidy at conception.
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Embryonic and Fetal Selection Against Aneuploidy
Most aneuploid embryos fail to develop due to natural selection during embryonic and fetal stages, leading to miscarriage or early pregnancy loss. This selective loss explains why aneuploidy is rarely observed in live births despite its high occurrence at conception.
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