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Lecture 12
Lecture 12

... Genes are short segments of DNA that determine our traits Sex chromosomes determine the sex (gender) of an individual and the remaining chromosomes are called AUTOSOMES. Female have XX (sex) chromosomes and 44 autosomes .Males have XY (sex) chromosomes and 44 autosomes.Dads determine the sex of a ch ...
Human genetic disorders
Human genetic disorders

... • A person with one sickle cell allele and one normal will have both types of hemoglobin. • A person with two sickle cell alleles will have the disease. ...
WINK Meiosis and Genetics
WINK Meiosis and Genetics

... Theme: Sex cells are formed by a process of cell division in which the number of chromosomes per cell is halved after replication. With the exception of sex chromosomes, for each chromosome in the body cells of a multicellular organism, there is a second similar, but not identical, chromosome. Altho ...
sexual reproduction and meiosis generates genetic variety by
sexual reproduction and meiosis generates genetic variety by

... ...
Fertilization and meiosis alternate in sexual life cycles
Fertilization and meiosis alternate in sexual life cycles

... Independent assortment alone would find each _____________________ chromosome in a _______________ that would be exclusively maternal or paternal in origin ...
Drosophila melanogaster Preferential Segregation of the Fourth
Drosophila melanogaster Preferential Segregation of the Fourth

... These should throw light on the mechanism concerned, but are not yet ready to report on. An unexpected result is that these preferences are very much reduced in the male, though apparently still present. In the two best-studied cases, ci eyR was preferred to gvl, the value being 52.9 0.8; eyD to gvl ...
OGT Boot Camp LIFE SCIENCE
OGT Boot Camp LIFE SCIENCE

... You should know ‘em by now! Animal Cell ...
Sex Linkage - The Grange School Blogs
Sex Linkage - The Grange School Blogs

... appearance, whether in male or female The remaining pair are the sex chromosomes ...
PowerPoint
PowerPoint

... Dominant and Recessive Traits • 2. Alleles may be dominant or recessive. The trait coded by a dominant allele is always expressed, while those of a recessive allele are only expressed when the two alleles are the same. • 3. When the two alleles are the same they are said to be homozygous. When they ...
What are genetic disorders?
What are genetic disorders?

... nonchromosomal DNA of mitochondria. • Each mitochondrion may contain 5 to 10 circular pieces of DNA. ...
BioH_Cell Division
BioH_Cell Division

... Anaphase: during a process called Disjunction, double-stranded chromosomes separate at their centromeres & begin to move toward opposite poles of the cell as Single-Stranded Chromosomes. By the end of anaphase, each pole of the spindle has a complete set of 46 single stranded chromosomes (equal to t ...
B2 6 Inheritance - misslongscience
B2 6 Inheritance - misslongscience

... 3. The characteristic that will show up in the offspring even if only one of the alleles is inherited. dominant ...
Unit 3- study guide Test 1
Unit 3- study guide Test 1

... of homologous pairs become entangled. This happens during the phase called ___________________. (It is the Homologous pair that is pulled apart during Anaphase I) 30. __________________- when the traits/genes (alleles for the trait) are represented ...
PGS: 274 – 284
PGS: 274 – 284

... A. This term refers to genes found on the sex chromosomes; 95% of the time it mainly refers to the X chromosome. (Think X when it is seX linked.) 1. This is because both sexes have at least one X chromosome in their genome. 2. XX (Female and homologous) ; XY (Male and heterologous) B. Sex chromosome ...
1. The ability to taste PTC, a bitter substance, is a dominant autosomal
1. The ability to taste PTC, a bitter substance, is a dominant autosomal

... 1. The ability to taste PTC, a bitter substance, is a dominant autosomal (not sexlinked) trait. A man who can taste PTC has a mother who cannot taste PTC. The man’s wife cannot taste the substance. What is the chance that their child will inherit the ability to taste PTC? 2. The w (white eye) gene i ...
أسئلة مساعدة للطلاب للاختبار النهائى
أسئلة مساعدة للطلاب للاختبار النهائى

... mRNA is produced in the process called: a) Respiration. b) Translation. c) Replication. d) Transcription. e) Transpiration ...
Genetics Exercises PDF
Genetics Exercises PDF

... describe using pool noodles to teach mitotis and meiosis, as shown below ...
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You Light Up My Life

... Human Genetic Analysis • Geneticists often gather information from several generations to increase the ...
Ch. 13 Reading Guide 9th edition
Ch. 13 Reading Guide 9th edition

... 3. Which type of reproduction will result in genetically identical offspring? Concept 13.2 Fertilization and meiosis alternate in sexual life cycles 4. What is a somatic cell? Give examples of two human somatic cell types. 5. How does a somatic cell compare to a gamete in terms of chromosome number? ...
unit 5 review sheet - Phillips Scientific Methods
unit 5 review sheet - Phillips Scientific Methods

... Structure found only in animal cells that the spindle fibers come from Event during Prophase I, when parts of homologous chromosomes trade pieces Reproduction involving only one parent Structure of two homologous chromosomes together during meiosis; has 4 chromatids Alternates between interphase and ...
xxZx*x
xxZx*x

... type, producing a chromosome number of 2n + 7. Turner syndrome A rare chromosomal disorder in females who have only one X chromosome. The syndrome is characterizedby short stature, the lack of sexual development at puberty, and heart abnormalities. zygote The diploid cell formed by the union of two ...
3. Chromosome Defects
3. Chromosome Defects

...  caused by misrepair of broken chromosomes, improper recombination, or improper segregation of chromosomes during mitosis or meiosis Chromosome abnormalities can affect  Germ cell (constitutional)  Somatic cell 1. Variation in chromosome number polyploidy: extra sets of chromosomes  1-3% of huma ...
3. Chromosome Defects
3. Chromosome Defects

...  caused by misrepair of broken chromosomes, improper recombination, or improper segregation of chromosomes during mitosis or meiosis Chromosome abnormalities can affect  Germ cell (constitutional)  Somatic cell 1. Variation in chromosome number polyploidy: extra sets of chromosomes  1-3% of huma ...
Meiosis
Meiosis

... • In mitosis, each daughter cell receives a complete set of chromosomes • In meiosis, homologous chromosomes separate to different daughter cells - the two alleles for each gene segregate randomly and end up in different gametes • The sorting and recombination of genes in meiosis result in a greater ...
GP3 Study Guide - Peoria Public Schools
GP3 Study Guide - Peoria Public Schools

< 1 ... 443 444 445 446 447 448 449 450 451 ... 538 >

Chromosome



A chromosome (chromo- + -some) is a packaged and organized structure containing most of the DNA of a living organism. It is not usually found on its own, but rather is complexed with many structural proteins called histones as well as associated transcription (copying of genetic sequences) factors and several other macromolecules. Two ""sister"" chromatids (half a chromosome) join together at a protein junction called a centromere. Chromosomes are normally visible under a light microscope only when the cell is undergoing mitosis. Even then, the full chromosome containing both joined sister chromatids becomes visible only during a sequence of mitosis known as metaphase (when chromosomes align together, attached to the mitotic spindle and prepare to divide). This DNA and its associated proteins and macromolecules is collectively known as chromatin, which is further packaged along with its associated molecules into a discrete structure called a nucleosome. Chromatin is present in most cells, with a few exceptions - erythrocytes for example. Occurring only in the nucleus of eukaryotic cells, chromatin composes the vast majority of all DNA, except for a small amount inherited maternally which is found in mitochondria. In prokaryotic cells, chromatin occurs free-floating in cytoplasm, as these cells lack organelles and a defined nucleus. The main information-carrying macromolecule is a single piece of coiled double-stranded DNA, containing many genes, regulatory elements and other noncoding DNA. The DNA-bound macromolecules are proteins, which serve to package the DNA and control its functions. Chromosomes vary widely between different organisms. Some species such as certain bacteria also contain plasmids or other extrachromosomal DNA. These are circular structures in the cytoplasm which contain cellular DNA and play a role in horizontal gene transfer.Compaction of the duplicated chromosomes during cell division (mitosis or meiosis) results either in a four-arm structure (pictured to the right) if the centromere is located in the middle of the chromosome or a two-arm structure if the centromere is located near one of the ends. Chromosomal recombination during meiosis and subsequent sexual reproduction plays a vital role in genetic diversity. If these structures are manipulated incorrectly, through processes known as chromosomal instability and translocation, the cell may undergo mitotic catastrophe and die, or it may unexpectedly evade apoptosis leading to the progression of cancer.In prokaryotes (see nucleoids) and viruses, the DNA is often densely packed and organized. In the case of archaea by homologs to eukaryotic histones, in the case of bacteria by histone-like proteins. Small circular genomes called plasmids are often found in bacteria and also in mitochondria and chloroplasts, reflecting their bacterial origins.
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