Category Archives: DNA

Gardenias newly sequenced genome highlights how evolutionary tinkering transforms plants into some of natures great chemical-makers.

Plants are some of natures most extraordinary chemists. Unlike animals, they cant run from predators or pathogens. They cant uproot themselves to seek out a mate or spread their seeds.

So instead, they manufacture chemicals: toxins to kill bacteria. Bitter alkaloids to ward off herbivores. Sweet nectar and jewel-colored pigments to draw in pollinators or birds that can help disperse seeds.

Chemicals, you could say, are one of a plants ways of making love and war.

But how did trees, shrubs and flowers obtain these capabilities?

In a new study, scientists explore this question through the evolution of the gardenia, Gardenia jasminoides, an evergreen shrub with white flowers thats planted as an ornamental in the tropics.

In a new study, researchers report sequencing the species genome. Credit: YW Low

Researchers sequenced the genome of the gardenia for the first time. Then, they looked in-depth at how the plant makes a compound called crocin. This brightly colored chemical,which gives saffron its vermillion hue, is also responsible for the red-orange shade of the gardenias ripened fruits.

The study identified the genes involved in making crocin and used them to create the compound in the lab. This work which included deciphering the step-by-step process that gardenias use to synthesize crocin lays the foundation for large-scale production of the chemical, which is thought to have medicinal properties as an antioxidant.

The research also explored the origins of crocin in gardenias. The findings, which will be published on June 18 inBMC Biology,highlight the power of an evolutionary process called tandem gene duplication, in which accidental copying of DNA gives organisms flexibility to expand the arsenal of genetic tools they have at their disposal. Its just one way that plants can evolve new capabilities, but its a crucial one.

The important principle is that plants can reinvent things, says study co-author Victor Albert, PhD, a University at Buffalo biologist. They can duplicate some parts of their genetic toolkit and twiddle the functions a little. So lets say you have a screwdriver, but the head is a super-big one. Imagine you could duplicate that screwdriver, but you could grind the head to make it smaller and useful for little screws, but you also still have the original one with the big head to handle large ones. Thats what these plants are doing.

A chemical compound called crocin gives the fruits their red-orange hue. Credit: YW Low

It was exciting to uncover these molecular tricks of the trade while researching the genome of a plant so important to traditional Chinese medicine, and now to modern biomedical research as well, says the studys co-corresponding author, Jingyuan Song, PhD, from the Engineering Research Center of Chinese Medicine Resource in China, who is also affiliated with the Chinese Academy of Medical Sciences and Peking Union Medical College.

The project was led by Song and Shilin Chen, PhD, from the Engineering Research Center of Chinese Medicine Resource and China Academy of Chinese Medical Sciences, and by Giovanni Giuliano, PhD, of the Italian National Agency for New Technologies, Energy and Sustainable Economic Development (ENEA). The first authors were Zhichau Xu, PhD, and Xiangdong Pu, both of the Chinese Academy of Medical Sciences and Peking Union Medical College. Xu is also affiliated with the Engineering Research Center of Chinese Medicine Resource.

Albert, professor of biological sciences in the UB College of Arts and Sciences and a visiting professor at Nanyang Technological University in Singapore, and his students made important contributions, conducting bioinformatics research that helped unravel the evolutionary history of crocin and caffeine synthesis in the gardenia and coffee plants, respectively.

In a tandem duplication event, a single gene gets replicated by mistake during reproduction. Then, as a species evolves over time, the excess DNA is free to mutate and take on new functions.

In Gardenia jasminoides, tandem duplication led to the evolution of a gene that is needed for crocin synthesis, the study concludes. This form of genetic replication also enabled a close relative of the gardenia the coffee plant Coffea canephora to develop caffeine-producing genes, according to the research, which compared the gardenias DNA to that of Coffea canephora and a few other plants.

This is a case where we see the same underlying evolutionary mechanism generating these tandem duplicates to create two different biosynthetic pathways of interest in two plants, Albert says. We have coffee and gardenia, which evolved from a close common ancestor, and in one case tandem duplicates formed and went crazy in coffee to make caffeine. And in the other, they formed and went crazy in gardenia to make crocins.

Made by plants, but useful for humans, too

Crocin is found not just in gardenias, but also in the crocus plant, which produces saffron. These species didnt inherit the ability to make crocin from a common ancestor: They evolved their arsenal of genes independently. The same goes for caffeine genes in coffee, tea and chocolate plants.

Plants are playing games with multiple evolutions of interesting phytochemicals, Albert says. And, of course, all of these phytochemicals are useful to the plants, maybe in fighting against pathogens or serving as attractants to insects.

When it comes to gardenias, the fiery color of the plants fruit helps to extend the species range, helping to attract animals that eat the fruits and expel the seeds in new locations.

But while plants perform chemistry for their own good, the compounds they produce can benefit humans too. Aspirin is closely related to a compound found in willow bark. Digoxin, used sparingly to treat heart problems, comes from the foxglove plant. Crocins antioxidant properties are of interest to researchers, and now, scientists have the knowledge they need to make that chemical in the lab.

Its a known fact that the same chemical (for instance, caffeine, or crocin) can appear again and again in distant plant species, says co-corresponding author Giuliano. One outstanding question was: How do the genes involved in the biosynthesis of such chemicals appear all at once in these different species? The work we published not only describes for the first time the complete pathway to crocin biosynthesis in any plant, but also shows that the pathway evolved in gardenias through the appearance of just one gene that acts early in the pathway, while the later ones were pre-existing, and were hitchhiked for making crocin. This is an elegant demonstration, at the biochemical level, of how nature reuses and adapts pre-existing mechanisms, rather than creating completely novel ones.

Reference: Tandem gene duplications drive divergent evolution of caffeine and crocin biosynthetic pathways in plants by Zhichao Xu, Xiangdong Pu, Ranran Gao, Olivia Costantina Demurtas, Steven J. Fleck, Michaela Richter, Chunnian He, Aijia Ji, Wei Sun, Jianqiang Kong, Kaizhi Hu, Fengming Ren, Jiejie Song, Zhe Wang, Ting Gao, Chao Xiong, Haoying Yu, Tianyi Xin, Victor A. Albert, Giovanni Giuliano, Shilin Chen and Jingyuan Song, 18 June 2020, BMC Biology.DOI: 10.1186/s12915-020-00795-3

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DNA Shows Plants Are Extraordinary Chemists Making Love and War - SciTechDaily

COLD SPRING HARBOR, N.Y., June 17, 2020 /PRNewswire/ -- An expansive new analysis of genetic variation among tomatoes has uncovered 230,000 previously hidden large-scale differences in DNA between 100 different varieties. As tomato plants evolved, segments of DNA were deleted, duplicated, or rearranged. These genomic "structural variations" underpin the vast diversity among tomatoes, changing flavors, altering yield, and shaping other important traits.

Tomatoes come in many sizes, colors, and flavors. CSHL Professor Zach Lippman, JHU Professor Mike Schatz, and colleagues around the world described the genetic underpinnings of 100 different types of tomatoes, including those in this photograph. Credit: Lippman lab/CSHL, 2020.

The study, a collaborative effort led by Cold Spring Harbor Laboratory (CSHL) Professor and Howard Hughes Medical Institute Investigator Zachary Lippman and Johns Hopkins University (JHU) Professor Michael Schatz, is the most comprehensive analysis of structural genome variation for a major crop. Breeders and scientists will be able to apply the information to breed or engineer new, more desirable plants with greater efficiency.

Large-scale differences between genomes, known collectively as structural variants, are likely responsible for a wide range of plant features that breeders care about, but these elements have been notoriously difficult to study, leaving much of the genetic origins of tomato diversity unexplained, says Xingang Wang, a postdoctoral researcher in Lippman's lab. New DNA sequencing technology along with powerful new genome editing technology has recently made structural variants easier to detect and study how they affect crop traits. Lippman's team, in collaboration with scientists at JHU, the University of Georgia, the Boyce Thompson Institute, and others, seized the opportunity to investigate.

Together, the group sequenced and compared the genomes of 100 different varieties of tomato, including robust varieties suitable for industrial agriculture, succulent heirlooms, and wild relatives of cultivated tomato.

To gain a better understanding of structural variants' role in diversity, the team showed that thousands of genes were changed by the structural variations. Then they used CRISPRthe genome editing tool that can make targeted changes in DNAto show that duplication of a particular gene causes a plant's tomatoes to increase in size by about 30 percent. Investigating another variant, they tracked down a gene that contributes to a smoky flavor in some tomatoes. And in another set of experiments, the researchers uncovered a complex interaction involving four structural variants that eliminates a trade-off between a feature that simplifies tomato harvesting and another that reduces productivity.

Understanding how these and other structural variants influence tomatoes gives breeders new power to improve the properties of tomatoes, a $190 billion global industry, and shows how structural variants that can enhance breeding are likely hidden in the complex genomes of many other important crops, like corn, rice, and soybeans.

About Cold Spring Harbor Laboratory

Founded in 1890, Cold Spring Harbor Laboratory has shaped contemporary biomedical research and education with programs in cancer, neuroscience, plant biology and quantitative biology. Home to eight Nobel Prize winners, the private, not-for-profit Laboratory employs 1,100 people including 600 scientists, students and technicians. For more information, visit http://www.cshl.edu.

About Johns Hopkins

Johns Hopkins is America's first research institution and a premier university and health system with campuses around the world.

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SOURCE Cold Spring Harbor Laboratory

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The DNA tricks that gave us 100 different kinds of tomatoes - Yahoo Finance

To 10-year-old Katie Krall, it just made sense. Her dad, who coached her softball team, should put his best hitter at leadoff and second-best hitter second. She figured if the best hitters were at the top of the order, theyd come to the plate the most and thats what youd want.

This was after the book Moneyball came out, but before the movie was released, so those kinds of thoughts, along with the importance of on-base percentage over batting average, had been in the ether but had yet to find their way to pee-wee softball. Shed read the book several years later, but at the time, Krall was just like many other 10-year-olds who liked to ask why and refused to accept the status quo just because itd always been that way. It portended a new type of baseball executive, a path that Krall, 23, would later find herself.

Krall swayed her dad, Darryl, and found herself batting second in the lineup behind her twin...

The rest is here:
Baseball's in her DNA: Reds operations analyst Katie Krall living a dream - The Athletic

I must have looked like hell.

I was walking across the grounds of Kennedy Meadows Resort Sunday just having come off the trail on my 15-mile day hike to Kennedy Lake and back. It is a hike most opt to do in two days so they can enjoy the lake in a setting surrounded by 9,000- to 11,000-foot peaks.

Two guys in their 20s that had been fishing nearby who had passed me up and were loading their gear in their pickup truck when I caught up asked if I wanted a lift to the trailhead parking lot still about a half mile away.

I thought about it for about a second and told them I appreciated the offer but no thanks. My right foot and right leg on the next step let me know what they thought of my turning the ride down.

A few minutes later a couple in a golf cart made the same offer. I again politely turned them down

When I got back to the car taking off my hiking boots was an adventure in pain. Due to two bunions that would make Paul Bunyan wince and a hammertoe that would spook Babe the Blue Ox, I have to cut up and apply a small fortune in moleskin to my toes as well as a nice pair of matching ankle spurs before I take off on Sierra hikes. They normally due to the trick but stretches of extremely muddy trails around the lake had managed to get both feet soaking wet.

That in its self would have made for an interesting return trip.

But even before I stepped out of the car that morning I knew I was going to be in for fun. Ive been walking from time-to-time with a slight limp during the past 10 months. Thats because a nice 15-foot semi-tumble downhill while scrambling at the end of last summer had aggravated a hereditary issue with my right leg. The need to cancel my annual trip to Death Valley last November due to work meant the only hikes with any degree of elevation gain and distance were ones I did tackling Mt. Diablo and nearby peaks which were nowhere tough enough to test my limits.

I was starting to hurt perhaps three miles shy of the turnaround point. My body was telling me to stop and go back. But I wasnt willing to do so.

I am clearly not athletic, coordinated or anywhere close to being someone who moves fast whether Im hiking or doing what passes for running. That said I can keep going.As for pain, its all relative. And given in my case it is more like a first cousin than something that is a stranger I tend to just deal with it.

As such I like to tell myself I have a high threshold of pain. But on Sunday I was beginning to think I was lying to myself.

It got to the point I had to slow my pace due to my leg hurting.

This is where most people will probably start thinking I am nuts. But unless something was broken or I was incapacitated in some manner I cant accept pain winning.

It is not mind over matter as much as understanding ones self.

I was fortunate enough to get a chance to explore pushing my limits 32 years ago in a research project a medical professional at Roseville Community Hospital was doing for his doctorate at the University of California, Davis.

Originally he had hoped to get athletic males from the hospital staff to severe as the six participants for a study to see the impacts on the body for someone who goes from rest to pushing it as hard as they can and sustaining it at the most strenuous predetermined level for five minutes.

Why he wasnt able to secure the number of participants he needed from the hospital staff for the nine-week project that required a once a week testing was the fact it required having eight spots on your chest shaved to connect you to all sorts of monitoring devices.

Although Im a candidate for the missing link, the shaving part did not bother me as I do not take by shirt off for fear of blinding pilots and causing planes to crash.

The hospital PR folks mentioned that I might by a good candidate given they knew I was bicycling 10,000 miles a year back then.

I agreed because quite frankly it sounded like a good story plus I was able to get a free platinum level physical complete with a cardiologist, water immersion body fat test, spot body fat measuring and assorted other prods and tests.

The treadmill test was interesting. The goal was to get my heart rate up to a sustained level at 85 percent of my maximum and stay there for two minutes. The goal was to do this within a 15-minute period.

I warned the cardiologist I sweat like theres no tomorrow. He said I probably wouldnt as I should hit the 85 percent threshold in six or so minutes. Seven minutes later I was dripping all over the place including on his work surface next to the treadmill when he handed me a tissue. Meanwhile he kept increasing the incline. It ended up taking the full 15 minutes before he got my heart rate where he wanted it.

The weekly tests involved using a Stairmaster. The length of the test was only five minutes max. Initially the weekly tests started with a minute warm-up before they started increasing the resistance. By the ninth week, you got no warm-up and the entire 5 minutes was spent on the highest setting for difficulty.

Afterwards, I was told they assumed Id be the weakest given how my body fat testing and general build stacked up against the others.

The other five were all active as runners or played basketball three or four times a week. All had played sports in high school.

It was then that I understood physical fitness and the ability to deal with or push through pain has nothing to do with being athletic or having been blessed with DNA that puts you in Greek god status.

It really is a matter of constantly pushing your limits.

In was tempted to accept a lift on Sunday but didnt. That wasnt because of pride but because I had to finish what I started. If Im by myself in the Sierra wilderness or in remote Death Valley canyon my mindset has to be I will get back to where I started under my own power.

That means listening to your body and making sure what it is telling you doesnt blind you from what you are capable of doing.

The real test, of course, is how you recover. My feet wanted to mutiny, my quads felt like I had just finished a double century cycling, and my right calf made a Charlie horse feel like a good thing later that night.

But 14 hours after completing the hike, I was able to take a 2 mile run and do so with no pain. That said sitting and simply walking for a few says after was anything but pain free.

The point of all this is simple. Pain shouldnt control your life.

See more here:
One doesn't have to win the DNA lottery to learn to deal with pain - Manteca Bulletin

News Release

Wednesday, June 17, 2020

DNA from uterine cells of women with endometriosis has different chemical modifications, compared to the DNA of women who do not have the condition, according to researchers funded by the National Institutes of Health. The changes involve DNA methylation the binding of compounds known as methyl groups to DNA which can alter gene activity. Moreover, the methylated DNA regions varied according to the stage, or severity, of endometriosis and responded differently to hormones involved in the menstrual cycle. Uterine responses to hormones influence pregnancy and other functions of uterine tissue.

The study was conducted by Linda C. Giudice, M.D., Ph.D., and colleagues at the University of California, San Francisco. It appears in PLOS Genetics. The study was funded by NIHs Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD).

The findings raise the possibility that differences in methylation patterns could one day be used to diagnose endometriosis and develop customized treatment plans for patients, said Stuart B. Moss, Ph.D., of NICHDs Fertility and Infertility Branch.

Endometriosis is a disease in which tissue similar to the lining of the uterus grows in other places in the body, such as on the ovaries, fallopian tubes or the bowels and bladder. It affects from 5 to 10% of women in the United States. Its main symptoms include pain, especially during menstrual periods, and infertility. Endometriosis is classified into four stages, ranging from minimal (stage I) to severe (stage IV). The only definitive way to diagnose endometriosis is with a surgical procedure called a laparoscopy.

The researchers analyzed a type of cell known as an endometrial stromal fibroblast, which regulates cells in the lining of the uterus. They compared methylation across DNA regions and differences in gene functioning in cells from women who did not have endometriosis or any other gynecological disorders to those of women with stage I endometriosis and of women with stage IV endometriosis. They also observed methylation patterns and gene functioning after the cells were exposed to estradiol (a form of estrogen) alone, progesterone alone, and to a combination of the two hormones to mimic changes in the levels of these hormones that occur during the menstrual cycle.

DNA methylation patterns and gene functioning differed among all groups of cells before exposure to the hormones, with exposure to each individual hormone, and to the combination of the two. The differences in methylation and gene functioning between stage I and stage IV endometrial cells could mean that the two may be distinct subtypes of endometriosis, rather than different degrees of the condition, Dr. Giudice added.

The data indicate that the proper interactions of hormones and DNA methylation are critical in normal uterine function, said the studys lead author, Sahar Houshdaran, Ph.D., University of California, San Francisco. The changes in these interactions that weve seen could play a role in the infertility that often accompanies endometriosis.

About the Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD): NICHD leads research and training to understand human development, improve reproductive health, enhance the lives of children and adolescents, and optimize abilities for all. For more information, visit https://www.nichd.nih.gov.

About the National Institutes of Health (NIH):NIH, the nation's medical research agency, includes 27 Institutes and Centers and is a component of the U.S. Department of Health and Human Services. NIH is the primary federal agency conducting and supporting basic, clinical, and translational medical research, and is investigating the causes, treatments, and cures for both common and rare diseases. For more information about NIH and its programs, visit http://www.nih.gov.

NIHTurning Discovery Into Health

Houshdaran S, et al. Steroid hormones regulate genome-wide epigenetic programming and gene transcription in human endometrial cells with marked aberrancies in endometriosis.PLOS Genetics. 2020.

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funded study links endometriosis to DNA changes - National Institutes of Health

Tahawwur Rana, the conspirator of the 26/11 attacks in Mumbai has been rearrested in the US and is likely to be extradited to India over his involvement in the 2008 terror attacks in which 166 people were killed.

The 59-year-old Pakistani-born Canadian was serving a 14-year-sentence and he was allowed early release from the prison after he told a US court that he has tested positive for COVID-19. However, he never made it out of prison.

Following an extradition request by India, where he has been declared a fugitive, he was rearrested on June 10.

Assistant US Attorney John J Lulejian informed the court that as per the bilateral Extradition Treaty signed in 1997, the government of India has requested the arrest and detention of Rana with a view towards his extradition, news agency PTI reported.

Rana is being prosecuted in India for a number of offences, including the conspiracy to commit murder, in violation of Sections 120B and 302, and murder in violation of Section 302 of the Indian Penal Code (IPC), Lulejian told the court.

As per the federal prosecutors, Rana participated in a conspiracy with his childhood friend David Coleman Headley, also known as 'Daood Gilani', and others to assist Pakistani terrorist organisations Lashkar-e-Taiba (LeT) and Harakat ul-Jihad-e-Islami, to carry out attacks in Mumbai.

He has been charged "with murder and murder conspiracy in India, according to court documents", he had however been cleared of the more serious charge of "providing support for the attacks in Mumbai."

"Rana's lawyer said at trial that he had been duped by his high school buddy, Headley, an admitted terrorist who plotted the Mumbai attacks. The defence called Headley, the government's chief witness who testified to avoid the death penalty, a habitual liar and manipulator," according to an article in The Washington Post.

He is also accused of assisting in a plot to carry out an attack on a Danish newspaper that printed cartoons on Prophet Muhammad in 2005. The plot could never be carried out.

(With ANI inputs)

Tahawwur Rana was first arrested in Chicago in 2009. He went to trial in the US District court for the Northern District of Illinois where Headley testified for the prosecution.

He was convicted of one count of conspiracy to provide material support to terrorism in Denmark and one count was of providing material support to Lashkar.

Thereafter, US District Judge for the Northern District of Illinois, Harry D Leinenweber, sentenced him to a 168-month prison term.

Another charge on Rana is a conspiracy to forge documents for the purpose of cheating and conspiracy to use as genuine a forged document or electronic record.

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Pak-origin 26/11 conspirator Tahawwur Rana arrested in US, likely to be extradited to India - DNA India

As with illness, prevention is always better than cure when it comes to skincare which is why we use shave cream to minimise razor burn and sunscreen to prevent wrinkles.

The ultimate preventative action, though, comes from understanding how your DNA affects your skin and hair so you can tailor your grooming regime to accommodate those quirks.

A CircleDNA test for example, revealed I have a high genetic risk of hyperpigmentation (had I known this years ago, Id have been extra-vigilant about sun protection) and a greater need for antioxidants molecules essential for healthy skin and hair.

Meanwhile, 23andMes test can tell you among other things whether youre prone to dandruff and bald spots. They may sound gimmicky but tools like these take some of the guesswork out of good grooming and could save you money in the long run. Great if, like me, thriftiness is in your genes.

DNA Genetic Analyses, 520, Lisa Franklin

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How DNA tests can set you on the path to healthy skin and hair - Telegraph.co.uk

Solar Eclipse on June 21: The entire world is bracing itself for the annular solar eclipse, which is popularly known as the "ring of fire" eclipse.

You can witness the Solar Eclipse or Surya Grahan 2020 on June 21 (Sunday).

The eclipse will begin at 9.15 am and it will end at 3.04 pm.

It will be the first solar eclipse of this year takes place on the summer solstice, which is the longest day in the Northern Hemisphere. While people living along the path annular eclipse passing through Anupgarh, Suratgarh, Sirsa, Jakhal, Kurukshetra, Yamunanagar, Dehradun, Tapowan and Joshimath will be able to see the annular phase, people in rest of India can witness a partial eclipse, said the Ministry of Science and Technology.

When Moon comes between the Sun and Earth, the shadow falls on the surface of the Earth. The Sun is entirely covered by the Moon for a brief period. Those places that are engulfed by the dark, dense umbral shadow of the Moon experience the total solar eclipse.

"Annular solar eclipse is a particular case of the total solar eclipse. Like the total solar eclipse, the Moon is aligned with the Sun. However, on that day, the apparent size of the Moon happens to be a wee smaller than the Sun. Hence the Moon covers the central part of the Sun, and the rim of the Sun appear like a 'ring of fire' in the sky for a very brief moment," Samir Dhurde of The Inter-University Centre for Astronomy and Astrophysics, Pune explained to ANI.

People living in Northern India will be able to witness the 'ring of fire' for 38 seconds. While, other parts of India will be able to see the total solar eclipse 2020 for around 82 seconds.

Apart from India, It can be witnessed in most parts of Africa, the Middle East and Asia.

Here are certain Dos and Donts we need to keep in mind while watching the eclipse.

1. Proper eye protection is needed to watch the solar eclipse as looking for a long period of time at the sun may damage your eyes.

2. A special solar filter on the lens is required to capture the eclipse.

3. If you are living in one of those countries where the solar eclipse cannot be sighted, it can also be watched virtually.

4. Don't look at the sun directly.

5. Don't look at the reflection of the sun in the water.

6. Ordinary sunglassed should not be used to witness the eclipse.

This year's annual solar eclipse will be particularly special as majority of the people will be couped up inside their homes amidst the coronavirus pandemic. Normally, people travel a great distance to observe the solar eclipse.

(With ANI inputs)

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Watch Solar Eclipse 2020: Here are the Dos and Don'ts to witness the grahan - DNA India

Neuroscientists from the Institute of molecular ophthalmology at Basel in Switzerland from stem cells with the DNA of Neanderthals raised miniature replicas of the brain. The experiments helped to determine the cause of the disappearance of this branch of the ancient people.

Experts have created a mini-copy of the on interspersed with the DNA of Homo neanderthalensis. The inhabitants of the Nordic countries, the researchers note, you can often find some variation of Neanderthal genes. This circumstance allows to assert, that we are talking about the gene structures, copies of which are inherited from those ancient people. Grayson camp, a paleontologist, spoke about the work of the research group. Neuroscientists were interested in the DNA related to hair and skin color. It is possible to examine the impact of segments of the genetic structures in the entire chain of the development of the human brain.

Neanderthals in contact with the ancient ancestors of the people left in human DNA, about 4% of their genes. For this reason, the tribes were able to adapt to survive in the North of the European continent. Scientists have concluded that Homo neanderthalensis could disappear because of genetic degeneration, not competing with CRO-magnon, as previously believed in the scientific world.

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In Switzerland neuroscientists raised a copy of the brain with the DNA of Neanderthals - The Times Hub

Atletico Madrid welcome Real Valladolid for their upcoming La Liga 2019-20 game.

Atletico Madrid will be eyeing to continue their winning run in todays game as they are 4th with 49 points. Real Valladolid, on the other side, with 33 points from 29 outings, are 13th on the league standings.

Where and when is theAtletico Madrid vs Real Valladolid, La Ligamatch being played?

TheAtletico Madrid vs Real Valladolid, La Ligamatch will be played on June 21, 2020, at Wanda Metropolitano Stadium.

What time does theAtletico Madrid vs Real Valladolid, La Ligamatch begin?

TheAtletico Madrid vs Real Valladolid, La Liga match will begin at 01:30 AM IST.

Where to watch Atletico Madrid vs Real Valladolid, La Liga live in India (TV channels)?

Unfortunately, theAtletico Madrid vs Real Valladolid, La Ligalive telecast won't be telecasted in India.

How and where to watch onlineAtletico Madrid vs Real Valladolid, La Liga live streaming?

TheAtletico Madrid vs Real Valladolid,La Ligalive telecast will be available online on Facebook to watch in India.

Atletico Madrid: Oblak; Trippier, Savic, Gimenez, Lodi; Correa, Thomas, Saul, Koke; Morata, Felix

Real Valladolid: Masip; Moyano, Fernandez, Salisu, Martinez; Plano, Alcaraz, Michel, Suarez; Unal, Guardiola

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Atletico Madrid vs Real Valladolid, La Liga: Live streaming, teams, Dream11, time in India (IST) & where to - DNA India