This document discusses balanced tertiary trisomics (BTT), which are a type of tertiary trisomic plant that can be used for hybrid seed production. Tertiary trisomics have an extra chromosome that is the result of a translocation. BTTs are constructed so that a dominant marker gene linked to the translocation breakpoint is on the extra chromosome. The two normal chromosomes carry recessive alleles. This allows BTTs to be distinguished from diploids for use in hybrid seed production schemes, such as one developed for barley where BTTs are male fertile and function as pollen parents, while diploids are male sterile and function as seed parents. The progeny of BTT selfing can then
The term balanced tertiary trisomic has three words of which (1) “trisomic” indicates the presence of extra chromosome, (2) “tertiary” indicates that the extra chromosome is a trans-located chromosome, and (3) “balanced” refers to the breeding behaviour of the trisomic.
Ramage defined the BTT as a tertiary trisomic constructed in such a way that the dominant allele of a marker gene, closely linked with the translocation breakpoint of the extra chromosome is carried on the extra chromosome, and the recessive allele is carried on the two normal chromosomes that constitute the diploid complement. The dominant marker gene may be located on the centromere segment or the trans-located segment of the extra chromosome.
The term balanced tertiary trisomic has three words of which (1) “trisomic” indicates the presence of extra chromosome, (2) “tertiary” indicates that the extra chromosome is a trans-located chromosome, and (3) “balanced” refers to the breeding behaviour of the trisomic.
Ramage defined the BTT as a tertiary trisomic constructed in such a way that the dominant allele of a marker gene, closely linked with the translocation breakpoint of the extra chromosome is carried on the extra chromosome, and the recessive allele is carried on the two normal chromosomes that constitute the diploid complement. The dominant marker gene may be located on the centromere segment or the trans-located segment of the extra chromosome.
Linkage and QTL mapping Populations and Association mapping population.
F2, Immortalized F2, Backcross (BC), Near isogenic lines (NIL), RIL, Double haploids(DH), Nested Association mapping (NAM), MAGIC and Interconnected populations.
Changes In Number And Structure Of Chromosomes SMGsajigeorge64
A brief account of the changes in number and structure of chromosomes : Haploidy, Polyploidy, Aneuploidy, Deletion, Duplication, Inversion and Translocation
KEY CONCEPTS
13.1 Offspring acquire genes from parents by inheriting
chromosomes
13.2 Fertilization and meiosis alternate in sexual life cycles
13.3 Meiosis reduces the number of chromosome sets from diploid to haploid
13.4 Genetic variation produced in sexual life cycles contributes to evolution
Linkage and QTL mapping Populations and Association mapping population.
F2, Immortalized F2, Backcross (BC), Near isogenic lines (NIL), RIL, Double haploids(DH), Nested Association mapping (NAM), MAGIC and Interconnected populations.
Changes In Number And Structure Of Chromosomes SMGsajigeorge64
A brief account of the changes in number and structure of chromosomes : Haploidy, Polyploidy, Aneuploidy, Deletion, Duplication, Inversion and Translocation
KEY CONCEPTS
13.1 Offspring acquire genes from parents by inheriting
chromosomes
13.2 Fertilization and meiosis alternate in sexual life cycles
13.3 Meiosis reduces the number of chromosome sets from diploid to haploid
13.4 Genetic variation produced in sexual life cycles contributes to evolution
Introduction, Types-somatic and germinal; Mechanism of meiotic crossing oversynapsis, duplication of chromosomes, breakage and union, terminalization;
Cytological basis of crossing over - Stern’s experiment in Drosophila; Creighton
and McClintock’s experiment in Maize; Crossing over in Drosophila, Construction
of genetic maps in Drosophila - two point and three-point crosses; Interference and
coincidence.
What is the possible reason that secondaries arise from parents that.pdfeyewaregallery
What is the possible reason that secondaries arise from parents that have unpaired chromosomes
but not from parents that are normal diploids? Map Genetics: A Conceptual Approach 6th
Edition Pierce MHE/Freeman presented by Sapling Learning Progeny of triploid tomato plants
often contain parts of an extra chromosome, in addition to the normal complement of 24
chromosomes. Mutants with a part of an extra chromosome are referred to as secondaries. James
and Margaret Lesley observed that secondaries arise from triploid (3n), trisomic (3n 1), and
double trisomic (3n 1 1) parents, but never from diploids (2n). (J. W. Lesley and M. M. Lesley.
1929. Genetics 14:321-336) What is a possible reason that secondaries arise from parents that
have unpaired chromosomes but not from parents that are normal diploids? Triploid and trisomic
conditions in tomato plants are unnatural, and this genomic imbalance leads to higher levels of
mitotic recombination. The trivalent chromosomes would still be able to associate through
chiasma prior to segregation during meiosis. Due to some unknown mechanism, triploid and
trisom c tomato plants O occasionally over-replicate part of a chromosome, which leads to the
generation of mutant tomato plants. Triploid and trisomic plants are vulnerable to infection by
the tomato mosaic O virus, so they acquire extra chromosomal material by the integration of
viral DNA, whereas diploid plants are not infected by the virus.
Solution
Ans: B
2n+1 condition is called trisomic in which an organism contains two complete genome + 1 extra
chromosome. During the process of meiosis 1 chromosomal page separate so that 1 members of
each state is distributed to one daughter nucleus and other members goes to other daughter
nucleus but rarely one pair of chromosomes fail to separate and moves to the pole giving half of
the daughter cells extra chromosome and remaining half lost one chromosome. As a result n - 1
and n+ 1 chromosomes appear. When the gamut with n+ 1 chromosome fuses with normal
gamut the resulting zygote will have 2n + 1 chromosomes producing trisomics organism.
It was found that trisomies or white study nature and studied in plants like tomatoes tobacco
wheat datura and so on..
Gene mutations – introduction – definition – a brief history – terminology –
classification of mutations – characteristic features of mutations – spontaneous
mutations and induced mutations
Gene mutations – artificial induction of mutations – physical and chemical
mutagens – molecular basis of mutations – detection of sex-linked lethals in
Drosophila by CLB technique – detection of mutations in plants – the importance of
mutation in plant breeding programmes –
Presentation on the relevance of self-incompatibility, methods to overcome self-incompatibility, advantages and disadvantages, utilization in crop improvement
Introduction:
RNA interference (RNAi) or Post-Transcriptional Gene Silencing (PTGS) is an important biological process for modulating eukaryotic gene expression.
It is highly conserved process of posttranscriptional gene silencing by which double stranded RNA (dsRNA) causes sequence-specific degradation of mRNA sequences.
dsRNA-induced gene silencing (RNAi) is reported in a wide range of eukaryotes ranging from worms, insects, mammals and plants.
This process mediates resistance to both endogenous parasitic and exogenous pathogenic nucleic acids, and regulates the expression of protein-coding genes.
What are small ncRNAs?
micro RNA (miRNA)
short interfering RNA (siRNA)
Properties of small non-coding RNA:
Involved in silencing mRNA transcripts.
Called “small” because they are usually only about 21-24 nucleotides long.
Synthesized by first cutting up longer precursor sequences (like the 61nt one that Lee discovered).
Silence an mRNA by base pairing with some sequence on the mRNA.
Discovery of siRNA?
The first small RNA:
In 1993 Rosalind Lee (Victor Ambros lab) was studying a non- coding gene in C. elegans, lin-4, that was involved in silencing of another gene, lin-14, at the appropriate time in the
development of the worm C. elegans.
Two small transcripts of lin-4 (22nt and 61nt) were found to be complementary to a sequence in the 3' UTR of lin-14.
Because lin-4 encoded no protein, she deduced that it must be these transcripts that are causing the silencing by RNA-RNA interactions.
Types of RNAi ( non coding RNA)
MiRNA
Length (23-25 nt)
Trans acting
Binds with target MRNA in mismatch
Translation inhibition
Si RNA
Length 21 nt.
Cis acting
Bind with target Mrna in perfect complementary sequence
Piwi-RNA
Length ; 25 to 36 nt.
Expressed in Germ Cells
Regulates trnasposomes activity
MECHANISM OF RNAI:
First the double-stranded RNA teams up with a protein complex named Dicer, which cuts the long RNA into short pieces.
Then another protein complex called RISC (RNA-induced silencing complex) discards one of the two RNA strands.
The RISC-docked, single-stranded RNA then pairs with the homologous mRNA and destroys it.
THE RISC COMPLEX:
RISC is large(>500kD) RNA multi- protein Binding complex which triggers MRNA degradation in response to MRNA
Unwinding of double stranded Si RNA by ATP independent Helicase
Active component of RISC is Ago proteins( ENDONUCLEASE) which cleave target MRNA.
DICER: endonuclease (RNase Family III)
Argonaute: Central Component of the RNA-Induced Silencing Complex (RISC)
One strand of the dsRNA produced by Dicer is retained in the RISC complex in association with Argonaute
ARGONAUTE PROTEIN :
1.PAZ(PIWI/Argonaute/ Zwille)- Recognition of target MRNA
2.PIWI (p-element induced wimpy Testis)- breaks Phosphodiester bond of mRNA.)RNAse H activity.
MiRNA:
The Double-stranded RNAs are naturally produced in eukaryotic cells during development, and they have a key role in regulating gene expression .
(May 29th, 2024) Advancements in Intravital Microscopy- Insights for Preclini...Scintica Instrumentation
Intravital microscopy (IVM) is a powerful tool utilized to study cellular behavior over time and space in vivo. Much of our understanding of cell biology has been accomplished using various in vitro and ex vivo methods; however, these studies do not necessarily reflect the natural dynamics of biological processes. Unlike traditional cell culture or fixed tissue imaging, IVM allows for the ultra-fast high-resolution imaging of cellular processes over time and space and were studied in its natural environment. Real-time visualization of biological processes in the context of an intact organism helps maintain physiological relevance and provide insights into the progression of disease, response to treatments or developmental processes.
In this webinar we give an overview of advanced applications of the IVM system in preclinical research. IVIM technology is a provider of all-in-one intravital microscopy systems and solutions optimized for in vivo imaging of live animal models at sub-micron resolution. The system’s unique features and user-friendly software enables researchers to probe fast dynamic biological processes such as immune cell tracking, cell-cell interaction as well as vascularization and tumor metastasis with exceptional detail. This webinar will also give an overview of IVM being utilized in drug development, offering a view into the intricate interaction between drugs/nanoparticles and tissues in vivo and allows for the evaluation of therapeutic intervention in a variety of tissues and organs. This interdisciplinary collaboration continues to drive the advancements of novel therapeutic strategies.
Multi-source connectivity as the driver of solar wind variability in the heli...Sérgio Sacani
The ambient solar wind that flls the heliosphere originates from multiple
sources in the solar corona and is highly structured. It is often described
as high-speed, relatively homogeneous, plasma streams from coronal
holes and slow-speed, highly variable, streams whose source regions are
under debate. A key goal of ESA/NASA’s Solar Orbiter mission is to identify
solar wind sources and understand what drives the complexity seen in the
heliosphere. By combining magnetic feld modelling and spectroscopic
techniques with high-resolution observations and measurements, we show
that the solar wind variability detected in situ by Solar Orbiter in March
2022 is driven by spatio-temporal changes in the magnetic connectivity to
multiple sources in the solar atmosphere. The magnetic feld footpoints
connected to the spacecraft moved from the boundaries of a coronal hole
to one active region (12961) and then across to another region (12957). This
is refected in the in situ measurements, which show the transition from fast
to highly Alfvénic then to slow solar wind that is disrupted by the arrival of
a coronal mass ejection. Our results describe solar wind variability at 0.5 au
but are applicable to near-Earth observatories.
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Slide 1: Title Slide
Extrachromosomal Inheritance
Slide 2: Introduction to Extrachromosomal Inheritance
Definition: Extrachromosomal inheritance refers to the transmission of genetic material that is not found within the nucleus.
Key Components: Involves genes located in mitochondria, chloroplasts, and plasmids.
Slide 3: Mitochondrial Inheritance
Mitochondria: Organelles responsible for energy production.
Mitochondrial DNA (mtDNA): Circular DNA molecule found in mitochondria.
Inheritance Pattern: Maternally inherited, meaning it is passed from mothers to all their offspring.
Diseases: Examples include Leber’s hereditary optic neuropathy (LHON) and mitochondrial myopathy.
Slide 4: Chloroplast Inheritance
Chloroplasts: Organelles responsible for photosynthesis in plants.
Chloroplast DNA (cpDNA): Circular DNA molecule found in chloroplasts.
Inheritance Pattern: Often maternally inherited in most plants, but can vary in some species.
Examples: Variegation in plants, where leaf color patterns are determined by chloroplast DNA.
Slide 5: Plasmid Inheritance
Plasmids: Small, circular DNA molecules found in bacteria and some eukaryotes.
Features: Can carry antibiotic resistance genes and can be transferred between cells through processes like conjugation.
Significance: Important in biotechnology for gene cloning and genetic engineering.
Slide 6: Mechanisms of Extrachromosomal Inheritance
Non-Mendelian Patterns: Do not follow Mendel’s laws of inheritance.
Cytoplasmic Segregation: During cell division, organelles like mitochondria and chloroplasts are randomly distributed to daughter cells.
Heteroplasmy: Presence of more than one type of organellar genome within a cell, leading to variation in expression.
Slide 7: Examples of Extrachromosomal Inheritance
Four O’clock Plant (Mirabilis jalapa): Shows variegated leaves due to different cpDNA in leaf cells.
Petite Mutants in Yeast: Result from mutations in mitochondrial DNA affecting respiration.
Slide 8: Importance of Extrachromosomal Inheritance
Evolution: Provides insight into the evolution of eukaryotic cells.
Medicine: Understanding mitochondrial inheritance helps in diagnosing and treating mitochondrial diseases.
Agriculture: Chloroplast inheritance can be used in plant breeding and genetic modification.
Slide 9: Recent Research and Advances
Gene Editing: Techniques like CRISPR-Cas9 are being used to edit mitochondrial and chloroplast DNA.
Therapies: Development of mitochondrial replacement therapy (MRT) for preventing mitochondrial diseases.
Slide 10: Conclusion
Summary: Extrachromosomal inheritance involves the transmission of genetic material outside the nucleus and plays a crucial role in genetics, medicine, and biotechnology.
Future Directions: Continued research and technological advancements hold promise for new treatments and applications.
Slide 11: Questions and Discussion
Invite Audience: Open the floor for any questions or further discussion on the topic.
Nutraceutical market, scope and growth: Herbal drug technologyLokesh Patil
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What are greenhouse gasses how they affect the earth and its environment what is the future of the environment and earth how the weather and the climate effects.
2. Trisomy:
•Trisomics are those organisms which have one extra chromosome (2n+1). Since
the extra chromosome may belong to any one of the different chromosome pairs,
the number of possible trisomics in an organism will be equal to the haploid
chromosome number.
•In a trisomic ,one of the pairs of chromosomes has an extra member and forms a
trivalent during anaphase I of meiosis.
•Two chromosomes will go to one pole and one chromosome will go to other pole
.As a result , two types of gametes are formed i.e. n and n+1.
•In plants the first case of trisomy was investigated in Jimsom weed i.e. Datura
stramonium by A.F. Blakeslee and J. Belling in1924.
•Datura (2n = 24) normally has 12 pairs of chromosomes in somatic cells. But in
an individual, they discovered 25 chromosomes.
3. •The size, shape and spine characteristics of seed capsule of this trisomic plant
were different from seed capsule of wild type species.
•Through experimental breeding, Blakeslee and his associates succeeded in
producing all 12 possible trisomics. When these were grown, each was found
to have a distinguishable phenotype that was attributed to extra set of genes
present on the extra chromosome contained in each of the 12 pairs of
chromosomes.
•An individual having two extra chromosomes each belonging to a different
chromosome pair is called double trisomic (2n + 1 + 1).
•Depending on the nature of extra chromosome, simple trisomics are of three
types.
a)Primary trisomics: The additional chromosome is normal one in primary
trisomics.
b)Secondary trisomics: Trisomics having isochromosome as additional
chromosome.
c)Tertiary trisomics: When additional chromosome in a trisomic is
translocated one, it is known as tertiary trisomic.
4.
5. Tertiary Trisomics:-
•When additional chromosome in a trisomic is translocated one, it is known as
tertiary trisomic.
•A tertiary trisomic individual consists of an interchanged non homologous
chromosome in addition to the normal somatic chromosome complement.
•Tertiary trisomics have been utilized effectively in tomato for determining
centromere positions on the linkage maps and for associating a gene with a
particular arm of a chromosome (Khush and Rick, 1967c).
•They have been used in barley for the construction of ―balanced tertiary
trisomics (BTTs) for hybrid seed production (Ramage, 1965).
•The first human trisomic syndrome discovered was the one involving ‘G‘ group
of chromosomes called Mongolism or Down‘s syndrome.
6. Sources of Tertiary Trisomics:
•In general, interchange heterozygotes that throw tertiary trisomics in their
progenies have been described in maize (Burnham, 1930, 1934), pea (Sutton,
1939), Oenothera lamarckiana (Emerson, 1936), Oenothera blandina
(Catcheside, 1954), Datura stramonium (Avery, Satina, and Rietsema, 1959),
barley (Ramage, 1960), tomato (Khush and Rick, 1967c; Gill, 1978), Phaseolus
vulgaris (Ashraf and Bassett, 1987), Pennisetum glaucum (Singh et al., 1982),
Secale cereale (Janse, 1985, 1987), and lentil (Ladizinsky, Weeden, and
Muehlbauer, 1990).
•Among the published results on tertiary trisomics, the investigation of Khush and
Rick (1967c) in tomato is the most thorough . They reported seven tertiaries; two
were isolated from tertiary monosomics and five from the interchanged
heterozygotes.
•In Datura, the tertiaries appeared spontaneously in a low frequency.
7. •Tertiary trisomics originate from an interchange heterozygote in the following
way. An interchange heterozygote occasionally forms a noncooriented
quadrivalent configuration at diakinesis and metaphase-I, and a 3:1 random
disjunction of chromosomes at anaphase-I will generate n + 1 gametes. Thus,
eight possible types of 2x + 1 individuals are expected in the progeny of a selfed
interchange heterozygote. Of the four tertiaries, two will be in homozygous
background and the other two in translocation heterozygous background.
•For isolating tertiaries in tomatoes, Khush and Rick (1967c) hybridized
interchanged heterozygotes with normal diploids. According to this procedure,
the progeny should segregate in a proportion of two tertiaries (homozygous) to
two primaries (interchange heterozygous) in the 2x + 1 fraction, and one normal
to one interchange heterzygote in the 2x fraction.
•A plant is designated as a primary trisomic if an extra chromosome is normal;
the trisomic may be a primary trisomic, a primary trisomic interchange
heterozygote, or a primary trisomic interchange homozygote. On the other hand,
if the extra chromosome is a translocated chromosome, a plant is designated as a
tertiary trisomic (Ramage, 1960).
8. BalancedTertiaryTrisomics:
•Ramage (1965) proposed a scheme utilizing balanced tertiary trisomics (BTT) for
production of hybrid barley seed.
•Balanced tertiary trisomics are tertiary trisomics constituted in such a way that the
dominant allele of a marker gene closely linked with the interchange breakpoint is
carried on the tertiary chromosome.
•The recessive allele is carried on each of the two normal chromosomes. The
dominant marker allele for a mature plant character, such as red plant color (R),
may be carried on either the centromere portion or on the interchanged segment of
the extra chromosome and should be linked with a male fertile gene (Ms).
•The two normal chromosomes should carry the corresponding recessive male
sterile allele (ms). All balanced tertiary trisomics would be male fertile and red,
and all diploids would be male sterile and green.
10. •All functioning pollen produced by the balanced tertiary trisomics would carry the
male sterile (ms) and the green plant color alleles (r).
•The self-progeny of such a trisomic would be planted in an isolation block.
•Diploid plants would be green and male sterile. All seed set on them would
produce male sterile diploids in the next generation.
•The diploid plants would be harvested separately, and seed produced on them
would be used to plant the female rows in the hybrid seed production field.
•Balanced tertiary trisomics planted in isolation would be dominant and would be
harvested separately.
•Seed produced on balanced tertiary trisomic plants would produce approximately
70% male sterile diploids and 30% balanced tertiary trisomics.
•This seed would be used to plant an isolation block the following year.
11. Prerequisites for utilizing BTT system in hybrid seed production
•The prerequisites for utilizing the BTT system in hybrid seed production are
that balanced tertiary trisomics produce abundant pollen and that during
anthesis, sufficient wind and insects are available for pollen dissemination.
Several other alternatives to distinguish tertiary trisomics from diploids have
been suggested, such as resistance or susceptibility to phytocides, seed size or
shape, and differential plant heights (Ramage, 1965).