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Unit 05 - Delivery guide
Unit 05 - Delivery guide

... One form of a gene; e.g. tall and dwarf are the alleles for the height of a pea plant. More than two alleles can exist for any specific gene, but only two of them will be found within any individual. ...
Patterns of Inheritance
Patterns of Inheritance

... Mendel performed thousands of crosses in pea plants with diering traits for a variety of characteristics. And he repeatedly came up with the same resultsamong the traits he studied, one was always dominant, and the other was always recessive. (Remember, however, that this dominantrecessive relati ...
Editorial - Ontario Association on Developmental Disabilities
Editorial - Ontario Association on Developmental Disabilities

... more about Down syndrome and the causes of both its non-medical and medical complications. Before antibiotic use and heart surgery, the average life expectancy for a person with Down syndrome was only about 9 years. With better medical care, many people with Down syndrome now live well into their 50 ...
Figure 20-6
Figure 20-6

... Sex chromosomes • There are two kinds of sex chromosomes, which determine the gender of the individual carrying them • They are generally called X and Y chromosomes, and differ in appearance, and genetic makeup (XX  female; XY  male) • During sexual reproduction the X and Y chromosomes behave as ...
DNA Duplication Associated with Charcot-Marie-Tooth Disease Type 1A. Lupski, et al., 1991 Cell, Vol. 66, 219-232, July 26, 1991,
DNA Duplication Associated with Charcot-Marie-Tooth Disease Type 1A. Lupski, et al., 1991 Cell, Vol. 66, 219-232, July 26, 1991,

... polymorphisms localized to the proximal region of chromosome 17p and a highly polymorphic marker on chromosome 1q were studied. In view of the demonstrated genetic heterogeneity, we required that each family provide independent evidence of linkage to a specific chromosomal region. Initial linkage an ...
Solid Tumour Section Nervous system: Astrocytic tumors Atlas of Genetics and Cytogenetics
Solid Tumour Section Nervous system: Astrocytic tumors Atlas of Genetics and Cytogenetics

... abnormalityis loss of the X and Y sex- chromosomes; loss of 22q is found in 20-30% of astrocytomas; other abnormalities observed in low grade tumors include gains on chromosome 8q, 10p, and 12p, and losses on chromosomes 1p, 4q, 9p, 11p 16p, 18 and 19. In anaplastic astrocytomas, chromosome gains or ...
Solving the shugoshin puzzle
Solving the shugoshin puzzle

... gene orientation, the class of orientation and intergenic distances. Furthermore, we asked whether the conservation of divergent gene orientation can be used for protein function prediction in eukaryotes. We based our study on a set of 19 fungi with a phylogenetic tree whose branches sum up to a tot ...
The Science of Psychology
The Science of Psychology

... behavior is governed by the consequences of the behavior. • Conventional morality - second level of Kohlberg’s stages of moral development in which the child’s behavior is governed by conforming to the society’s norms of behavior. • Postconventional morality - third level of Kohlberg’s stages of mor ...
F 1 - OpenWetWare
F 1 - OpenWetWare

... Suppose you’ve been hired by a horse breeder who wants to produce a line of true-breeding palomino horses—palomino horses that, when crossed with each other, always produce palomino foals. The breeder has 12 palomino stallions that are not related to each other. He tells you that every one of the tw ...
A preanaphase role for a Cks/Suc1 in acentrosomal spindle
A preanaphase role for a Cks/Suc1 in acentrosomal spindle

... absence of conventional centrosomes (McKim & Hawley, 1995). Instead, chromosomes have a central role in the assembly of spindle microtubules. This acentrosomal (also called acentriolar or anastral) spindle formation is common in female meiosis for many animals including mammals, insects and worms. D ...
Heredity in Fingerprints
Heredity in Fingerprints

... The cell is the unit of structures and the unit of heredity. Chromosomes in all of the body cells of a single individual are alike. Thus, the individual functions as a single unit —alike in every cell yet different from all other people. Under extremely high magnification, crossbands on the chromoso ...
CIS Curriculum Maps - Central School District 51
CIS Curriculum Maps - Central School District 51

... 4. Understand and explain the different nitrogen base in a nucleotide and the order of the bases make DNA segments different from each other. Therefore, different expressions of genes are produced. 5. Differentiate between the scientific contributions of Dr. Rosalind Franklin vs. Watson and Crick. 6 ...
Slide 1
Slide 1

... It is only a coincidence; most other organisms have an odd number of chromosomes. The diploid chromosome number is even because of mitosis. The diploid chromosome number represents pairs of chromosomes, one from each parent, so it is an even number. Chromosome numbers double in cells every time the ...
Effects of linkage on response to directional selection from new
Effects of linkage on response to directional selection from new

Assisted Conception
Assisted Conception

... • Aneuploidy – Having less than or more than normal diploid number of chromosomes • Monosomy • Trisomy • Triploidy ...
SEX-DETector: a probabilistic approach to uncover sex
SEX-DETector: a probabilistic approach to uncover sex

... Although this RNA-seq cross-based strategy is very promising for studying sex chromosomes in nonmodel organisms, the existing approaches have a number of limitations due to the fact that inference of sex-linkage was done with empirical filters and without a statistical framework. Once RNA-seq reads ...
Excellence exemplar
Excellence exemplar

... If you need more space for any answer, use the page(s) provided at the back of this booklet and clearly number the question. Check that this booklet has pages 2-13 in the correct order and that none of these pages is blank. ...
Developmental and genetic disorders in
Developmental and genetic disorders in

... where fusion occurs between two acrocentric chromosomes with the loss of genetic information from the short arms of participating chromosomes (Mak and Jarvi, 1996). Base pair mutations can occur in all genes. Substitution or deletion of a single base sequence in a strand of DNA can have a profound i ...
Lesson 17: Patterns of Inheritance (3
Lesson 17: Patterns of Inheritance (3

... Lesson 17: Patterns of Inheritance (3.2.2) GENES AND INHERITANCE Genes, which are specific portions of DNA, determine hereditary characteristics. Genes carry traits that can be passed from one generation to the next. Alleles are different forms of a gene. Two alleles make up one gene. For every trai ...
some inconvenient truths about sex chromosome dosage
some inconvenient truths about sex chromosome dosage

... meant by sex chromosome dosage compensation. Sex chromosome dosage compensation is a mechanism, acting in the heterogametic sex, to increase transcription of the single X or Z chromosome to that level expected from a diploid complement. Empirical tests of dosage compensation often assess the gene ex ...
How does chromosome behavior account for Mendel`s Principles ?
How does chromosome behavior account for Mendel`s Principles ?

... with a white-eyed male fly. Half of the male and half of the female offspring were red-eyed, and half of the male and half of the female offspring were white-eyed. What was the genotype of the female fly? ...
Evolution on the X chromosome: unusual patterns and processes
Evolution on the X chromosome: unusual patterns and processes

... which males carry two heteromorphic sex chromosomes (such as X and Y) and females carry two copies of the same chromosome (XX). ...
NONE - Ontario College of Family Physicians
NONE - Ontario College of Family Physicians

... • NIPT cannot: ―Completely rule out aneuploidy ―Detect chromosome differences other than aneuploidy of chromosomes 13, 18, 21, X and Y ―Detect single gene conditions ―Detect congenital anomalies ...
Unit 4 – Genetics – Chapter Objectives (13,14,15) from C
Unit 4 – Genetics – Chapter Objectives (13,14,15) from C

... Chapter 13 Meiosis & Sexual Life Cycles The Basis of Heredity 1. Explain in general terms how traits are transmitted from parents to offspring. 2. Distinguish between asexual and sexual reproduction. The Role of Meiosis in Sexual Life Cycles 3. Distinguish between the following pairs of terms: a. so ...
(2013). Nothing in genetics makes sense except in light of genomic
(2013). Nothing in genetics makes sense except in light of genomic

... was envisioned to be a hereditary “blueprint” consisting of indivisible genes linearly arranged on chromosomes and containing only the information needed to transform a fertilized egg into a functional adult. As advances in mapping and sequencing technology allowed the “black box” of the genome to b ...
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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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