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chapter 15 - Issaquah Connect
chapter 15 - Issaquah Connect

... For most genes, it is a reasonable assumption that a specific allele will have the same effect regardless of whether it is inherited from the mother or father. However, for a few dozen mammalian traits, phenotype varies depending on which parent passed along the alleles for those traits. ...
Genetics Lecture presentation
Genetics Lecture presentation

... • Phenotype = Genetics + Environment (+GxE interactions) • Genotype = the genetic makeup of the organism ...
13_lecture_meiosis
13_lecture_meiosis

... gamete) have 23 pairs of chromosomes • A karyotype is an ordered display of the pairs of chromosomes from a cell • The two chromosomes in each pair are called homologous chromosomes, or homologs • Chromosomes in a homologous pair are the same length and shape and carry genes controlling the same inh ...
File
File

... • Traits are characteristics you inherit from your parents; • This means your parents pass some of their characteristics on to you through genes ...
The Mysteries of Life
The Mysteries of Life

... replications of the original organism. This can be a good trait, because if a “bad” trait gets passed on, an organism will not be able to live for long. The disadvantage of this process is also the fact that genetic variation is not allowed. For example, if they want to go to a new environment very ...
AP Biology - Naber Biology
AP Biology - Naber Biology

... parental combination. These genes will be transmitted as a unit and will not sort independently. However, during meiosis, crossing over occurs between homologous chromosomes, and the linked genes can become “unlinked.” In general, the farther two genes are from each other along the chromosome, the m ...
BIOLOGY 2013-‐2014 FINAL EXAM STUDY GUIDE
BIOLOGY 2013-‐2014 FINAL EXAM STUDY GUIDE

... Explain  what  a  cell  plate  does  and  where  it  would  be  found   ...
Exam 4 Review KEY
Exam 4 Review KEY

Klinefelter Syndrome - Western States Genetics Services Collaborative
Klinefelter Syndrome - Western States Genetics Services Collaborative

... each pair comes from the father’s sperm cell and the other comes from the mother’s egg cell. In other words, the baby receives half its genetic material from the mother and half from the father. When the chromosomes are examined in the laboratory under the microscope, they look like this: ...
Chapter 15 Assignment - kyoussef-mci
Chapter 15 Assignment - kyoussef-mci

... In fruit fly genetics, the normal fly is called a "wild type" and any fly exhibiting a phenotypic mutation is called a "mutant". Mutant flies are given names that generally denote the type of mutation the fly exhibits. For example, the mutant "ebony" has a much darker body than the wild type fly. E ...
BIOL 105 S 2014 QZM2 QA 140207.1
BIOL 105 S 2014 QZM2 QA 140207.1

... 32. The urinary system is exclusive to the A) gonads. B) ducts that receive and transport the gametes. C) accessory glands and organs that secrete fluids. D) external genitalia. E) female urethra. 33. ________ are formed at the end of meiosis. A) Spermatogonia B) Primary spermatocytes C) Spermatids ...
Molecular Biology of the Cell
Molecular Biology of the Cell

... amphibian oocyte. •A special form of chromosomes, found in oocytes of most animals (except mammals). •Seen at early meiosis stage due to an active transcription of many genes. •DNA are organized into a series of large chromatin loops, emanating from a chromosomal axis. Early in oocyte differentiatio ...
Meiosis II - Solon City Schools
Meiosis II - Solon City Schools

... Replication of chromosomes • Replication is the process of duplicating a chromosome • Occurs prior to division • Replicated copies are called sister chromatids • Held together at centromere ...
A T C G - National Angus Conference
A T C G - National Angus Conference

... Chromosomes • 29 pairs Autosomal • 1 pair sex chromosomes (XX or XY) • 1 set from each parent ...
Chromosomes and inheritance
Chromosomes and inheritance

... colorblindness (ONE from each parent). Why is it that the sons could be more prone to colorblindness? He must inherit (receive) only ONE recessive allele. This is due to there being no gene for color vision on the Y chromosome. ...
Pathology
Pathology

... cardiovascular abnormalities, oocyte degredation (none by 2yr), and ovaries are converted to fibrous streaks (uterus+ normal) ...
Retrogenes reveal the direction of sex-chromosome
Retrogenes reveal the direction of sex-chromosome

... evolved independently multiple times in both animals and plants (BULL 1983; CHARLESWORTH 1996; RICE 1996). Sex chromosomes are thought to evolve from a pair of autosomes that acquire a new sex-determining locus. Theory suggests that natural selection will favor tight linkage between the newly arisen ...
ABG301
ABG301

... 1. Each parent contributes one factor of each trait shown in offspring. 2. The two members of each pair of factors segregate from each other during gamete formation. 3. Males and females contribute equally to the traits in their offspring. 4. The blending theory of inheritance was not correct. 5. Ac ...
Study Guide EXAM #1
Study Guide EXAM #1

... 2- Describe what a karyotype is and how it can be used in prenatal diagnosis? 3 - How is the gender genetically determined? Understand the function of the SRY gene. 4 - What is the difference between genetic abnormalities and genetic disorders? 5 - Understand the various symbols used in a pedigree c ...
Mitotic Cell Division - Jocha
Mitotic Cell Division - Jocha

... in one the nuclear content, the DNA, is divided in two new nuclei by means of a very specific sequence of events. In the second part, called cytokinesis, the cytoplasm of the cell is split in two and two new cells are produced from the original one. There are two types of nuclear division processes ...
Chapter 13: Genetic Technology
Chapter 13: Genetic Technology

...  Clone – genetically identical offspring produced from a single cell  In 1997 Scottish scientist Ian Wilmut cloned first mammal, a sheep named Dolly ...
Tetrad Genetics
Tetrad Genetics

... The equal left and right arms are called 2L and 2R, and 3L and 3R Each arm carries ~20% of the gene of the fly Y is heterochromatic – few genes, fertility factors XO is a viable sterile male Sex is determined by the X:autosome ratio (not the presence of a Y, as in humans) There is recombination in f ...
Chapter 24 Genetics and Genomics Genotype and
Chapter 24 Genetics and Genomics Genotype and

... Pleiotrophy and Genetic Heterogeneity Pleiotropy •  single genetic disorder producing several symptoms •  Marfan syndrome is an example •  people affected produce several symptoms that vary Genetic Heterogeneity •  same phenotype resulting from the actions of different genes •  hereditary deafness i ...
The green dwarf parent in Cross2 is from a true
The green dwarf parent in Cross2 is from a true

... One-two sentence explanation/defense of your answer (no credit if no explanation): A trait is said to be monogenic if the phenotypic variation between two individuals or two strains of organisms can be explained by differences in a single gene. In this example, a single malfunctioning gene can resul ...
F 1 Generation
F 1 Generation

... other blood groups are derived from it. Group A is the second oldest blood group, appearing around 25,000 - 15,000BC, when larger human settlements first appeared as farming developed. You'll find a lot of A in Central and Eastern Europe. It's the commonest group in Norway, Denmark, Austria, Armenia ...
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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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