1) Spermatogenesis and oogenesis both involve meiosis to produce haploid gametes from diploid germ cells.
2) In spermatogenesis, spermatogonia undergo mitosis and differentiate into spermatocytes, then spermatids through meiosis. Spermiogenesis transforms spermatids into mature sperm.
3) In oogenesis, oogonia become primary oocytes that arrest in prophase I until after puberty. A few complete meiosis I and II if fertilized, becoming ovulated ova.
1. Spermatogenesis (Spermatocytogenesis, Spermiogenesis, Spermiation, Shape and function of cells inside the Testis, Semen and sperm structure, Sperm journey after synthesis to outside)
Implantation and placentation , and overviewPranjal Gupta
Implantation and formation of placenta is an essential developmental process during human embryogenesis as it marks the connection between maternal and fetal blood, a condition specific to mammals more precisely eutherians. It works as a passage of required nutrients to the growing embryo and collection of its waste. It also discusses various types of placenta that are seen in mammals.
In testis, the immature male germ cell (spermatogonia ) produce sperms by spermatogenesis
The spermatogonia ( sing. Spermatogonium ) present on the inside of seminiferous tubules multiply by mitotic division and increase in numbers
Each spermatogonium is diploid and contains 46 chromosomes
Some of the spermatogonia called primary spermatocytes periodically undergo meiosis.A primary spermatocyte completes the first meiotic division (reduction division) leading to formation of two equal, haploid cells called secondary spermatocyte, which have only 23 chromosomes
The secondary spermatocyte undergo the second meiotic division to produce four equal, haploid spermatids
1. Spermatogenesis (Spermatocytogenesis, Spermiogenesis, Spermiation, Shape and function of cells inside the Testis, Semen and sperm structure, Sperm journey after synthesis to outside)
Implantation and placentation , and overviewPranjal Gupta
Implantation and formation of placenta is an essential developmental process during human embryogenesis as it marks the connection between maternal and fetal blood, a condition specific to mammals more precisely eutherians. It works as a passage of required nutrients to the growing embryo and collection of its waste. It also discusses various types of placenta that are seen in mammals.
In testis, the immature male germ cell (spermatogonia ) produce sperms by spermatogenesis
The spermatogonia ( sing. Spermatogonium ) present on the inside of seminiferous tubules multiply by mitotic division and increase in numbers
Each spermatogonium is diploid and contains 46 chromosomes
Some of the spermatogonia called primary spermatocytes periodically undergo meiosis.A primary spermatocyte completes the first meiotic division (reduction division) leading to formation of two equal, haploid cells called secondary spermatocyte, which have only 23 chromosomes
The secondary spermatocyte undergo the second meiotic division to produce four equal, haploid spermatids
Reproductive and hormonal functions of the male Maryam Fida
Reproductive and hormonal functions of the male 1. Primary Sex Organs
Testes are the primary sex organs or gonads in males.
Accessory Sex Organs
Accessory sex organs in males are:
1. Seminal vesicles 2. Prostate gland
3.Urethra 4. Penis
Testis contain Seminiferous Tubules. Sperms are formed in seminiferous tubules. Testis has two important types of cells. 1.Sertoli cells are the supporting cells in seminiferous tubules. Sertoli cells provide support, protection and nourishment for the spermatogenic cells present in seminiferous tubules. Sertoli cells contain hormone “INHIBIN”. 2. Leydig cells. When stimulated by LH, they secrete:
Testosterone
Androstenedione
Dehydroepiandrosterone (DHEA)
Embryology-all basic definition,Stage wise development of fetus,development o...sonal patel
Embryology-all basic definition,Stage wise development of fetus,development of Zygote stage ,development of Embrionic Stage ,development of Fetus Stage all are according week development,Amnione,chorion,Fetal layer, Umbilical Cord developmentmade By sonal Patel
Reproductive and hormonal functions of the male Maryam Fida
Reproductive and hormonal functions of the male 1. Primary Sex Organs
Testes are the primary sex organs or gonads in males.
Accessory Sex Organs
Accessory sex organs in males are:
1. Seminal vesicles 2. Prostate gland
3.Urethra 4. Penis
Testis contain Seminiferous Tubules. Sperms are formed in seminiferous tubules. Testis has two important types of cells. 1.Sertoli cells are the supporting cells in seminiferous tubules. Sertoli cells provide support, protection and nourishment for the spermatogenic cells present in seminiferous tubules. Sertoli cells contain hormone “INHIBIN”. 2. Leydig cells. When stimulated by LH, they secrete:
Testosterone
Androstenedione
Dehydroepiandrosterone (DHEA)
Embryology-all basic definition,Stage wise development of fetus,development o...sonal patel
Embryology-all basic definition,Stage wise development of fetus,development of Zygote stage ,development of Embrionic Stage ,development of Fetus Stage all are according week development,Amnione,chorion,Fetal layer, Umbilical Cord developmentmade By sonal Patel
Embryology Course I - Introduction, Gametogenesis, ImplantationRawa Muhsin
This is is the first session of a basic human embryology course, and it discusses:
1. Gametogenesis (both spermato- and oo-genesis)
2. Fertilization
3. Implantation of the zygote in the uterine wall
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.
A brief information about the SCOP protein database used in bioinformatics.
The Structural Classification of Proteins (SCOP) database is a comprehensive and authoritative resource for the structural and evolutionary relationships of proteins. It provides a detailed and curated classification of protein structures, grouping them into families, superfamilies, and folds based on their structural and sequence similarities.
The increased availability of biomedical data, particularly in the public domain, offers the opportunity to better understand human health and to develop effective therapeutics for a wide range of unmet medical needs. However, data scientists remain stymied by the fact that data remain hard to find and to productively reuse because data and their metadata i) are wholly inaccessible, ii) are in non-standard or incompatible representations, iii) do not conform to community standards, and iv) have unclear or highly restricted terms and conditions that preclude legitimate reuse. These limitations require a rethink on data can be made machine and AI-ready - the key motivation behind the FAIR Guiding Principles. Concurrently, while recent efforts have explored the use of deep learning to fuse disparate data into predictive models for a wide range of biomedical applications, these models often fail even when the correct answer is already known, and fail to explain individual predictions in terms that data scientists can appreciate. These limitations suggest that new methods to produce practical artificial intelligence are still needed.
In this talk, I will discuss our work in (1) building an integrative knowledge infrastructure to prepare FAIR and "AI-ready" data and services along with (2) neurosymbolic AI methods to improve the quality of predictions and to generate plausible explanations. Attention is given to standards, platforms, and methods to wrangle knowledge into simple, but effective semantic and latent representations, and to make these available into standards-compliant and discoverable interfaces that can be used in model building, validation, and explanation. Our work, and those of others in the field, creates a baseline for building trustworthy and easy to deploy AI models in biomedicine.
Bio
Dr. Michel Dumontier is the Distinguished Professor of Data Science at Maastricht University, founder and executive director of the Institute of Data Science, and co-founder of the FAIR (Findable, Accessible, Interoperable and Reusable) data principles. His research explores socio-technological approaches for responsible discovery science, which includes collaborative multi-modal knowledge graphs, privacy-preserving distributed data mining, and AI methods for drug discovery and personalized medicine. His work is supported through the Dutch National Research Agenda, the Netherlands Organisation for Scientific Research, Horizon Europe, the European Open Science Cloud, the US National Institutes of Health, and a Marie-Curie Innovative Training Network. He is the editor-in-chief for the journal Data Science and is internationally recognized for his contributions in bioinformatics, biomedical informatics, and semantic technologies including ontologies and linked data.
Earliest Galaxies in the JADES Origins Field: Luminosity Function and Cosmic ...Sérgio Sacani
We characterize the earliest galaxy population in the JADES Origins Field (JOF), the deepest
imaging field observed with JWST. We make use of the ancillary Hubble optical images (5 filters
spanning 0.4−0.9µm) and novel JWST images with 14 filters spanning 0.8−5µm, including 7 mediumband filters, and reaching total exposure times of up to 46 hours per filter. We combine all our data
at > 2.3µm to construct an ultradeep image, reaching as deep as ≈ 31.4 AB mag in the stack and
30.3-31.0 AB mag (5σ, r = 0.1” circular aperture) in individual filters. We measure photometric
redshifts and use robust selection criteria to identify a sample of eight galaxy candidates at redshifts
z = 11.5 − 15. These objects show compact half-light radii of R1/2 ∼ 50 − 200pc, stellar masses of
M⋆ ∼ 107−108M⊙, and star-formation rates of SFR ∼ 0.1−1 M⊙ yr−1
. Our search finds no candidates
at 15 < z < 20, placing upper limits at these redshifts. We develop a forward modeling approach to
infer the properties of the evolving luminosity function without binning in redshift or luminosity that
marginalizes over the photometric redshift uncertainty of our candidate galaxies and incorporates the
impact of non-detections. We find a z = 12 luminosity function in good agreement with prior results,
and that the luminosity function normalization and UV luminosity density decline by a factor of ∼ 2.5
from z = 12 to z = 14. We discuss the possible implications of our results in the context of theoretical
models for evolution of the dark matter halo mass function.
This pdf is about the Schizophrenia.
For more details visit on YouTube; @SELF-EXPLANATORY;
https://www.youtube.com/channel/UCAiarMZDNhe1A3Rnpr_WkzA/videos
Thanks...!
Nutraceutical market, scope and growth: Herbal drug technologyLokesh Patil
As consumer awareness of health and wellness rises, the nutraceutical market—which includes goods like functional meals, drinks, and dietary supplements that provide health advantages beyond basic nutrition—is growing significantly. As healthcare expenses rise, the population ages, and people want natural and preventative health solutions more and more, this industry is increasing quickly. Further driving market expansion are product formulation innovations and the use of cutting-edge technology for customized nutrition. With its worldwide reach, the nutraceutical industry is expected to keep growing and provide significant chances for research and investment in a number of categories, including vitamins, minerals, probiotics, and herbal supplements.
Observation of Io’s Resurfacing via Plume Deposition Using Ground-based Adapt...Sérgio Sacani
Since volcanic activity was first discovered on Io from Voyager images in 1979, changes
on Io’s surface have been monitored from both spacecraft and ground-based telescopes.
Here, we present the highest spatial resolution images of Io ever obtained from a groundbased telescope. These images, acquired by the SHARK-VIS instrument on the Large
Binocular Telescope, show evidence of a major resurfacing event on Io’s trailing hemisphere. When compared to the most recent spacecraft images, the SHARK-VIS images
show that a plume deposit from a powerful eruption at Pillan Patera has covered part
of the long-lived Pele plume deposit. Although this type of resurfacing event may be common on Io, few have been detected due to the rarity of spacecraft visits and the previously low spatial resolution available from Earth-based telescopes. The SHARK-VIS instrument ushers in a new era of high resolution imaging of Io’s surface using adaptive
optics at visible wavelengths.
5. Sperm are produced within the seminiferous
tubules.
Interspersed within the tubules are large
cells which are the sustentacular cells
(sertoli's cells), which support and nourish
the other cells.
Spermatogenesis takes 65–75 days
6. Early in embryonic development, primordial germ
cells enter the testes and differentiate into
spermatogonia
It begins with the spermatogonia, which contain the
diploid (2n) number of chromosomes.
Spermatogonia - Stem cells - when they undergo
mitosis, some spermatogonia remain near the
basement membrane of the seminiferous tubule in an
undifferentiated state to serve as a reservoir of cells
for future cell division and subsequent sperm
production.
The rest of the spermatogonia lose contact with the
basement membrane, squeeze through the tight
junctions of the blood–testis barrier, undergo
developmental changes, and differentiate into
primary spermatocytes.
Primary spermatocytes, like spermatogonia, are
diploid (2n); that is, they have 46 chromosomes.
7. Each primary spermatocyte replicates its DNA and then meiosis
begins.
The two cells formed by meiosis I are called secondary
spermatocytes.
Each secondary spermatocyte has haploid number (n) i.e 23
chromosomes.
Each chromosome within a secondary spermatocyte, however, is
made up of two chromatids (two copies of the DNA) still attached
by a centromere.
No replication of DNA occurs in the secondary spermatocytes.
In meiosis II, the chromosomes line up in single file along the
metaphase plate, and the two chromatids of each chromosome
separate.
The four haploid cells resulting from meiosis II are called
spermatids. A single primary spermatocyte therefore produces
four spermatids via two rounds of cell division (meiosis I and
meiosis II).
8.
9. A unique process occurs during spermatogenesis.
As spermatogenic cells proliferate, they fail to
complete cytoplasmic separation (cytokinesis).
The cells remain in contact via cytoplasmic
bridges through their entire development.
This pattern of development- synchronized
production of sperm in any given area of
seminiferous tubule.
It may also have survival value in that half of the
sperm contain an X chromosome and half contain
a Y chromosome.
The larger X chromosome may carry genes
needed for spermatogenesis that are lacking on
the smaller Y chromosome.
10. The final stage of spermatogenesis, spermiogenesis, is the
development of haploid spermatids into sperm.
No cell division occurs in spermiogenesis; each spermatid
becomes a single sperm cell.
During this process, spherical spermatids transform into
elongated, slender sperm.
An acrosome forms atop the nucleus, which condenses and
elongates, a flagellum develops, and mitochondria multiply.
Sertoli cells dispose of the excess cytoplasm that
sloughs off.
Finally, sperm are released from their connections to
Sertoli cells, an event known as spermiation.
Sperm then enter the lumen of the seminiferous tubule.
Fluid secreted by Sertoli cells pushes sperm along their
way, toward the ducts of the testes.
At this point, sperm are not yet able to swim.
11.
12. Each day about 300 million sperm
complete the process of
spermatogenesis.
Head contains nucleus with 23 highly
condensed chromosomes
Acrosome- a caplike vesicle filled with
enzymes (hyaluronidase and
proteases)- help a sperm to penetrate
a secondary oocyte to bring about
fertilization.
Neck - behind the head - contains
centrioles -form the microtubules that
comprise the remainder of the tail
Middle piece- contains mitochondria
arranged in a spiral – provide the
energy (ATP) for locomotion of sperm
13. The formation of gametes in the ovaries is
termed OOGENESIS
In contrast to spermatogenesis, which begins in
males at puberty, oogenesis begins in females
before they are even born.
Oogenesis occurs in essentially the same
manner as spermatogenesis,
Meiosis takes place and the resulting germ
cells undergo maturation.
14.
15. During early fetal development, primordial (primitive) germ
cells migrate from the yolk sac to the ovaries- differentiate
within the ovaries into OOGONIA
Oogonia are diploid (2n) stem cells that divide mitotically to
produce millions of germ cells.
Even before birth, most of these germ cells degenerate in a
process known as atresia
A few develop- larger cells called primary oocytes that enter
prophase of meiosis I during fetal development but do not
complete that phase until after puberty.
During this arrested stage of development, each primary
oocyte is surrounded by a single layer of flat follicular cells,
and the entire structure is called a primordial follicle
The ovarian cortex surrounding the primordial follicles
consists of collagen fibers and fibroblast-like stromal cells.
The remainder of the primary oocytes undergo atresia.
16.
17. Each month after puberty until menopause,
gonadotropins (FSH and LH)- stimulate the
development of several primordial follicles,
A few primordial follicles start to grow,
developing into primary follicles
Each primary follicle consists of a primary
oocyte - surrounded by several layers of cells
called granulosa cells. The outermost
granulosa cells rest on a basement membrane.
As the primary follicle grows- forms a clear
glycoprotein layer- zona pellucida between the
primary oocyte and the granulosa cells.
In addition, stromal cells surrounding the
basement membrane begin to form an
organized layer called the theca folliculi.
18.
19. On maturation - primary follicle develops into a
secondary follicle.
Secondary follicle - the theca differentiates into two
layers:
› Theca interna - highly vascularized- secrete
estrogens
› Theca externa - outer layer of stromal cells and
collagen fibers.
Granulosa cells - secrete follicular fluid - builds up in a
cavity - antrum in the center of the secondary follicle.
The innermost layer of granulosa cells - firmly attached
to the zona pellucida - corona radiata
20.
21.
22. The secondary follicle - becomes larger, turning into
a mature (graafian) follicle
Just before ovulation, the diploid primary oocyte
completes meiosis I, producing two haploid (n) cells
of unequal size—each with 23 chromosomes
› The smaller cell produced by meiosis I, called the
first polar body, is essentially a packet of
discarded nuclear material.
› The larger cell, known as the secondary oocyte,
receives most of the cytoplasm.
Once a secondary oocyte is formed, it begins
meiosis II but then stops in metaphase.
The mature (graafian) follicle soon ruptures and
releases its secondary oocyte, a process known as
OVULATION.
23. At ovulation, the secondary oocyte is expelled into the
pelvic cavity then into the uterine tube together with the first
polar body and corona radiata.
If fertilization does not occur, the cells degenerate.
If sperm are present- penetrates the secondary oocyte -
meiosis II resumes.
The secondary oocyte splits into two haploid cells, of
unequal size- larger cell ovum, or mature egg & the
smaller one is the second polar body.
The nuclei of the sperm cell and the ovum then unite,
forming a diploid zygote.
First polar body undergoes another division to produce
two polar bodies.
The primary oocyte ultimately gives rise to three haploid
polar bodies - all degenerate, and a single haploid ovum.
Thus, one primary oocyte gives rise to a single gamete
(an ovum).