Define these pairs of terms, and distinguish between them.aneuploidy/euploidymonosomy/trisomyPatau syndrome/Edwards syndromeautopolyploidy/allopolyploidyautotetraploid/amphidiploidparacentric inversion/pericentric inversion
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Define these pairs of terms, and distinguish between them.
aneuploidy/euploidy
monosomy/trisomy
Patau syndrome/Edwards syndrome
autopolyploidy/allopolyploidy
autotetraploid/amphidiploid
paracentric inversion/pericentric inversion
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- Discuss the following sets of terms: a. trisomy and triploidy b. aneuploidy and polyploidyShown below are photomicrographs of Rhoeo tradescantia cells undergoing meiosis. Answer the following question for each of the photomicrographs: Identify the cytogenetic abnormality observed (ex. ring, chain, laggard, bridge). Identify the meiotic stage in which these aberrations are observed (as shown in the photomicrograph). Explain how these aberrations are formed and relate to the possible causal mutation(s). Will this result to sterile and/or fertile gametes? Explain.Define nondisjunction and explain how it causes aneuploidy. Name two syndromes resulting from aneuploidy
- Consider a diploid organism that follows the XX-XO mode of sex determination. Normally, there are 7 chromosomes in its somatic cell. The chromosomal composition is as follows: Chromosome I is a large acrocentric chromosome Chromosome II is a large telocentric chromosome Chromosome III is a small telocentric chromosome Chromosome IV (X chromosome) is a medium submetacentric chromosome Aneuploidy was observed in a particular individual wherein there are three copies of Chromosome III. Diagram how aneuploidy may occur through Mitosis starting from a parent cell at G1 phase. Make sure to distinguish between chromosomes and the following phases of cell division (G1 phase, prophase, metaphase, anaphase, telophase, cytokinesis). Indicate the chromosome equation and chromosome number of the parent cell and the daughter cells. *S phase and G2 phase purposefully excludedConsider a diploid organism that follows the XX-XO mode of sex determination. Normally, there are 7 chromosomes in its somatic cell. The chromosomal composition is as follows: Chromosome I is a large acrocentric chromosome Chromosome II is a large telocentric chromosome Chromosome III is a small telocentric chromosome Chromosome IV (X chromosome) is a medium submetacentric chromosome Aneuploidy was observed in a particular individual wherein there are three copies of Chromosome III. Illustrate the source of aneuploidy if it occurs in Meiosis I. Diagram spermatogenesis starting with the primary spermatocyte up to spermatozoa, making sure to distinguish between chromosomes and the different phases of meiosis I (prophase I*, metaphase I, anaphase I, telophase I). Indicate the respective chromosome equation and chromosome number of the primary spermatocyte, secondary spermatocyte, spermatid, and spermatozoon.Meiosis is characterized by the pairing of homologouschromosomes during prophase I. In many species, an elaboratestructure called the synaptonemal complex forms betweenhomologues. During this pairing, homologues may exchangechromosomal material at sites called chiasmata. In meiosis I, thehomologues separate from each other, reducing the chromosomenumber to the haploid state (thus the reductive division). It isfollowed by a second division without replication, during whichsister chromatids become separated. The result of meiosis I and IIis four haploid cells. If sister chromatids separated at the first division, would meiosis still work?
- Match the following: A duplicated chromosome is made of 2.A maternal and paternal chromosome present together, each with two sister chromatids 3.Semi-condensed DNA made up of coiled nucleosomes. 4.Super-coiled DNA strands. 5.Contains only one copy of each chromosome. 6.Name of an error during meiosis resulting in fewer chromosomes than normal in a zygote or individual (2n-1) 7.General term for an error resulting in the incorrect number of chromosomes in a gamete after meiosis 8.A specific version of a gene, such as blue eye colour 9.A region on a chromosome that codes for a protein 10.Region where chromosomes are attached 11.None of the above (should be selected more than once) with monosomy trisomy aneuploidy centromere gene sister chromatids diploid Haploid tetrad telomere Chromosomes Chromatin alleleConsider and individual with 3 pairs of homologous chromosomes labeled as: A/a B/b D/d(where the slash line separates one chromosome from its homologues). How many differentmeiotic products (sperm or egg) can this individual produce? What are these?Consider the true diploid plant cell (2n=4) below. The paternally derived blue chromosomesare of two types, metacentric and acrocentric. These chromosomes contain the same gene pattern andstructural features as the maternally derived purple chromosomes. Consider two genes A and B whichare found on the metacentric and acrocentric chromosome pairs, respectively. Assume the father passedon A and B alleles, and the mother passed on a and b alleles. a. Show the possible loci of these genes (specify alleles) on the image. Label both sister chromatids in each chromosome. (Note: Sister chromatids are products of replication.)b. Draw the four possible gametes formed after meiosis assuming there was no crossing over. Label the gene loci.
- Chromosomal abnormalities can interfere with pairing and segregation of homologous chromosomes in meiosis and so lead to infertility problems and unbalanced mutations in gametes. In which of the following do problems occur only when homologous regions recombine, instead of during the simple pairing and segregation of homologous chromosomes? Group of answer choices Paracentric inversions Robertsonian translocations Translocations Odd multiples of autopolyploidy Allopolyploidy with differing n numbers of chromosomesWhich of the following is false? Group of answer choices With a pericentric inversion, there is no loss in genetic material. Haploinsufficiency is caused by a duplication event causing increased expression of a gene. An effect of aneuploidy is that it changes the dosages of some genes. Pseudodominance indicates that one of the homologous chromosomes has a deletion. Sterility is a possible effect of autopolyploidyIdentify the type of chromosomal aberration described in each of the following cases: a. loss of a chromosome segment b. extra copies of a chromosome segment c. reversal in the order of a chromosome segment d. movement of a chromosome segment to another, nonhomologous chromosome