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Unit 30C Cell Division, Genetics, and Molecular
Unit 30C Cell Division, Genetics, and Molecular

... diagram in Figure 3. Condensed chromosomes may be either unduplicated or duplicated. In a duplicated chromosome, the original chromosome and its duplicate are attached to each other by a structure called the centromere. While attached to one another, the two chromosome duplicates are called sister c ...
Why Compare sequences?
Why Compare sequences?

... (20 aa and a terminator), the information is sharpened up considerably. The 'wrongframe' information is discarded, and third-base degeneracies are consolidated. All in all, the signal-to-noise ratio is greatly improved for the specific purpose of identifying protein relatives. It is accepted that co ...
1 - Miss Jan`s Science Wikispace
1 - Miss Jan`s Science Wikispace

...  Draw diagrams to illustrate substitution, insertion, deletion and addition as gene mutations  Describe the effects of substitution, insertion, deletion and addition gene mutations  Explain what chromosomal mutations are  Explain the difference between chromosomal block and number mutations  Dr ...
Evolutionary Origin and Adaptive Function of Meiosis
Evolutionary Origin and Adaptive Function of Meiosis

... Natural bacterial transformation involves the transfer of DNA from one bacterium to another through the surrounding medium. Transformation depends on the expression of numerous bacterial genes whose products appear to be designed to carry out this process (Chen and Dubnau, 2004; Johnsborg et al., 20 ...
Lesson 1.1: Mutation
Lesson 1.1: Mutation

... From the previous lesson you learned about how DNA codes for proteins, which are ultimately responsible for all of your physical structure. There’s so much variation in organisms because each gene on a chromosome may have two or more alleles, different forms of that gene. For example, purple and whi ...
2q13 microduplications
2q13 microduplications

... in ‘copy number variant’ databases such as DECIPHER (DatabasE of genomiC varIation and Phenotype in Humans using Ensembl Resources; https:// decipher.sanger.ac.uk). Such databases are used by geneticists and clinicians to report anonymised genetic conditions, with consent, so the possible outcomes o ...
Influence of the environment and probes on rapid DNA sequencing
Influence of the environment and probes on rapid DNA sequencing

... by sampling the current with the driving field off. The distributions of these currents, with this particular pore geometry, for all four bases are shown in the top section of Figure 3, assuming each current is measured instantaneously.∗∗ We can see that these distributions are unique, but overlappi ...
Molecular Mechanisms of Plant and Microbe Coexistence
Molecular Mechanisms of Plant and Microbe Coexistence

... reporter bacteria responding specifically to individual amino acids. The induction of a lysine-responsive P. putida reporter was demonstrated in rhizosphere of corn, but not in the bulk soil (Espinosa-Urgel and Ramos 2001) and a tryptophan-reporter strain showed significant induction in older root s ...
Lehninger Principles of Biochemistry
Lehninger Principles of Biochemistry

... both DNA and RNA are hydrophilic. The hydroxyl groups of the sugar residues form hydrogen bonds with water. The phosphate groups, with a pKa near 0, are completely ionized and negatively charged at pH 7, and the negative charges are generally neutralized by ionic interactions with positive charges o ...
Chromatin insulators: lessons from the fly
Chromatin insulators: lessons from the fly

... example, it is possible that as cells differentiate, insulator-mediated changes in nuclear organization precede or accompany cell differentiation and may be crucial in the establishment and/or maintenance of specific patterns of gene expression. If this is the case, cells must possess mechanisms to ...
Prospective diagnostic analysis of copy number variants using SNP
Prospective diagnostic analysis of copy number variants using SNP

... the probable cause of ASD, based on their large size, absence from healthy individuals, de novo occurrence and/or presence in previously reported syndromes associated with ID and ASD: a de novo triplication of the 15q11–q12 region in a male subject (family 772), a deletion of the 9p24 region in a fe ...
PDF - International Journal of Medical Sciences
PDF - International Journal of Medical Sciences

... variation and immune evasion. However, in our previous studies, proteins MPT64, PstS1, Rv0309 and Rv2945c all harbored higher numbers of amino acid substitutions in their T cell epitopes, which suggests their roles in ongoing immune evasion. Here, we used the same set of 180 clinical M. tuberculosis ...
View/Open
View/Open

... expression of the gene is occurred due to polymorphism in promoter region. A number of QTLs for glucosinolate biosynthesis and activation (Lambrix et al. 2001; Kliebenstein et al. 2001; Kroymann et al. 2003; Zhang et al. 2006;), phosphate sensing (Svistoonoff et al. 2007), and flowering time (Johan ...
ppt - University of Connecticut
ppt - University of Connecticut

... Exon - a region of a gene which is translated into protein Intron - a region of a gene which is not translated into protein Splicing – a process in which the introns are removed and exons are joined to be translated into a single protein ...
Rebuttal - MIT Technology Review
Rebuttal - MIT Technology Review

... 2) SENS omits oxidative damage to proteins No – that is included, under intracellular and extracellular indigestible molecules (’junk’).2,3 Oxidatively damaged proteins that do not fall under those headings are, by definition, broken down and their constituent amino acids reused if undamaged and exc ...
16S rRNA characterization of Bacillus strain and its
16S rRNA characterization of Bacillus strain and its

... processes. It also entails a variety of genes responsible for microbial tolerance or defense against extreme conditions or xenobiotics present in the media. In a previous work, Bacillus spp. isolated from textile wastewater was exploited in terms of characterization, tolerance to pH, salinity, cold ...
Genetics: The Science of Heredity
Genetics: The Science of Heredity

... Mendel showed that organisms have two alleles for every trait. (One that we get from mom and one that we get from dad). He also showed that these alleles can be either dominant or recessive. Capital letters are used to represent dominant alleles and lower case letters are used to represent recessive ...
RESEARCH ARTICLES Characterization of the Long
RESEARCH ARTICLES Characterization of the Long

... selection among 31 amino acid properties in the three lineages of interest. TreeSAAP allows us to identify these property changes and classify them into categories on a gradient from conservative to radical change. Based on data set– specific nucleotide substitution patterns, a neutral model of expe ...
The plant genome`s methylation status and response to stress
The plant genome`s methylation status and response to stress

... siRNA generate methylcytosine variation Variation for cis-acting transposons and direct repeats can cause one genotype to have methylation at loci that are not methylated within a second genotype. RNAi components are required to maintain these differences. For example, the A. thaliana Landsberg erec ...
Lesson08Phylogenetics
Lesson08Phylogenetics

... among various groups of organisms ...
Mendelian and Non-Mendelian Regulation of Gene Expression in
Mendelian and Non-Mendelian Regulation of Gene Expression in

... expression levels of 22,242 genes that were detected in both parents and at least 90% of the IBM RILs. The mean expression levels in the RILs were similar to the mid-parent values for most genes (Figure 1B). Transgressive segregation, defined here as at least 10% of RILs exhibiting expression levels ...
8-chromo_struct variation [Autosaved]
8-chromo_struct variation [Autosaved]

... • the genes on the normal homologue are hemizygous: there is only 1 copy of those genes, and thus they are expressed even if recessive (like genes on the X in male mammals). • Heterozygous deletions are aneuploid, because the genes in the deleted region are present in only 1 copy instead of the norm ...
Minireview Alpha Satellite and the Quest for the Human Centromere
Minireview Alpha Satellite and the Quest for the Human Centromere

... the importance of centromeres to cell and organismal viability, there should be no room for gain or loss of centromere function. Then why would centromeres utilize epigenetic mechanisms of regulation? Perhaps because it is adaptive and advantageous during evolution. Epigenetic mechanisms could help ...
A disproportionate role for mtDNA in DobzhanskyMuller
A disproportionate role for mtDNA in DobzhanskyMuller

... hybrid fitness and ultimately reproductive isolation upon secondary contact. The Dobzhansky–Muller (DM) model nicely accounts for the evolution of such incompatibilities. Although DM incompatibilities were originally conceived as resulting of interactions between nuclear genes, recent studies have d ...
Advances in genetics show the need for extending screening
Advances in genetics show the need for extending screening

... for the (ADH) studies in which a LOD score .3.3 is required (threshold for complex traits), since this means that a large number of individuals is needed for the analysis.15,16 Another means of identifying novel ADH genes is through genome-wide association studies. This approach received substantial ...
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Gene



A gene is a locus (or region) of DNA that encodes a functional RNA or protein product, and is the molecular unit of heredity. The transmission of genes to an organism's offspring is the basis of the inheritance of phenotypic traits. Most biological traits are under the influence of polygenes (many different genes) as well as the gene–environment interactions. Some genetic traits are instantly visible, such as eye colour or number of limbs, and some are not, such as blood type, risk for specific diseases, or the thousands of basic biochemical processes that comprise life.Genes can acquire mutations in their sequence, leading to different variants, known as alleles, in the population. These alleles encode slightly different versions of a protein, which cause different phenotype traits. Colloquial usage of the term ""having a gene"" (e.g., ""good genes,"" ""hair colour gene"") typically refers to having a different allele of the gene. Genes evolve due to natural selection or survival of the fittest of the alleles.The concept of a gene continues to be refined as new phenomena are discovered. For example, regulatory regions of a gene can be far removed from its coding regions, and coding regions can be split into several exons. Some viruses store their genome in RNA instead of DNA and some gene products are functional non-coding RNAs. Therefore, a broad, modern working definition of a gene is any discrete locus of heritable, genomic sequence which affect an organism's traits by being expressed as a functional product or by regulation of gene expression.
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