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MIT labs win top recognition for sustainable practices in cold storage management

Whitehead Institute and MIT named 2020 Organizational Winners in the fourth annual International Institute for Sustainable Laboratories International Laboratory Freezer Challenge.

Environment, Health and Safety Office
December 9, 2020

In its fourth year, the International Institute for Sustainable Laboratories (I2SL) International Laboratory Freezer Challenge drew 218 laboratory participants from around the world, from 88 research institutions. Three MIT laboratories participated in the challenge: the Department of Biology’s Barbara Imperiali Lab, Department of Biological Engineering’s Jacquin Niles Lab, and Department of Biology/Whitehead Institute for Biomedical Research’s David Sabatini Lab. MIT and the Whitehead Institute together received the Top Academic Organization Award. The Niles lab and the Imperiali lab are MIT Environment, Health & Safety (EHS) Green Lab Certified.

The Freezer Challenge, which is run by the nonprofit organizations My Green Labs and I2SL, is aimed at promoting efficient, effective sample storage for laboratories around the world, and using a spirit of friendly competition to increase sample accessibility, sample integrity, reduced costs, and energy efficiency.

Over a five-month period, challenge contestants implement optimal cold storage management practices, such as defrosting and removing dust from freezer intake or coils, regular cleanouts, organization of inventory on file, and high-density storage. Winners are then chosen based on the amount of energy saved. Additionally, in the spirit of friendly competition and collaboration that pervades the challenge, contestants can earn points for sharing tips about their own cold storage best practices.

This year, the 218 laboratory participants saved an estimated total of 3.2 million kilowatt-hours (kWh) per year, up from 2.4 million in 2019. The savings represents the equivalent of reducing carbon emissions by 2,260 metric tons per year, or removing 360 passenger vehicles from the road for a year. According to Christina Greever, operations manager at My Green Labs, the three participating MIT and Whitehead Institute labs saved an estimated 520 kWh/year.

Two of the three labs — Niles and Imperiali — have previously participated in MIT EHS’ Green Labs Freezer Challenge, and have consequently instituted good management practices surrounding cold storage. The Sabatini lab hasn’t previously participated in EHS’ challenge, but had also already implemented many of the practices the challenge encourages and rewards.

Edith Valeri, of the Sabatini lab, said that while her lab didn’t face any major difficulties, the challenge encouraged lab management staff to be “more aware of freezer usage” and “more mindful of wattage usage, turning down temperatures to a sustainable level, and defrosting the freezers.”

Similarly, both Sebastian Smick, a technical associate in the Niles lab, and Christine Arbour, an NIH postdoc in the Imperiali lab, found that participating in the challenge was not disruptive to operations, and the only difficulties they ran into came as a result of the Covid response. Because of their previous participation in  the MIT EHS’ Green Labs Freezer Challenge, efficient energy usage is already routine for the three labs.

Smick described the challenge as “a good incentive” for the Niles lab to practice regular thawing, and “a nice way to quantify what it means to the University’s power consumption.” He credits MIT Custodial Services for the invaluable support they provide on a regular basis. “Custodial Services is always there for us during our thaws to provide mopping and absorbent barriers while we thaw. Most of the ice is captured as a solid, but spillover is unavoidable. They’ve saved us thousands of paper towels!”

The Imperiali lab upgraded its cold storage in March, replacing its minus-80 degrees Celsius freezer with a newer, more energy efficient model, and entered the challenge ready to focus on maximizing that investment. “Our lab consistently cleans our freezer filters, -80 degree C freezer in particular, to prevent the compressor from overworking,” says Arbour. “We are also vigilant with appropriate chemical storage. We store chemicals at the temperature that the supplier/company recommends and nothing colder. This prevents overcrowding in –20 and –80 degree C freezers, which can start to add up!”

For Smick, a key takeaway from the challenge was the quantification of the power consumption of his lab’s cold storage. “I was so surprised when I first learned about the power consumption of our -80 C and -20 freezers,” he recalls. “It’s easy to see the impact of changing to a cheaper reagent or eliminating a wasteful process when it is something that comes directly out of your pocket, but electricity is something we take for granted; it should be conserved like any natural resource, and this challenge really shines an environmentally friendly, zero-energy consumption light on how easy it is to make a huge impact.”

Smick credits the challenge with inspiring his lab to conduct regular thaws, a major energy-saving practice. “I know for a fact that, prior to our regular freezer thaws which we started doing because of this competition, we were throwing away thousands of dollars of reagents away each year because they were lost in the glaciers that we were maintaining in our freezers.”

Similarly, Arbour says the Imperiali lab will continue to implement the practices recognized in the challenge. “Our lab practices will continue to evolve with new green practices,” she says. “Our entire lab is invested in doing better for the environment.”

“My hope is that competitions like this inspire MIT and the entire world to take a more serious look about how we deal with the resources available to us: from electricity to recyclable waste,” says Smick. “Science generates a huge amount of waste, and there is so much more that we can do to reduce environmental impact, and to offset the cost of generating meaningful data.”

MIT EHS has plans in the works for the enhancement and expansion of the Institute’s Green Labs program, and will be implementing them in the upcoming year. Labs interested in learning more about the Green Labs program, its benefits, and details on how to participate should contact environment@mit.edu.

A good environment for sustainable research
Whitehead Institute
December 3, 2020

From floods to forest fires to droughts, the consequences of climate change are affecting people and ecosystems around the globe, and these events will only grow more abundant in the coming decades. Researchers in many scientific fields are studying this complex problem from different angles. Whitehead Institute primarily focuses on biomedical research, and yet in recent years researchers in several labs here have discovered ways in which their work might contribute to climate resilience and sustainability. Scientists here are applying their skills to problems of climate change and sustainability in medicine, agriculture, and beyond. Learn more about their work in the stories below:

FEEDING A CHANGING WORLD

Researchers in Whitehead Institute Member Mary Gehring’s lab hope to help address the problem of global food security as the human population grows and the effects of climate change threaten agriculture. They are exploring new ways to engineer crops so they will thrive in the conditions created by climate change. Read about them here.

NATURE’S LIBRARY: THE VALUE OF BIODIVERSITY TO BIOLOGICAL RESEARCH

Climate change and other human activities have endangered many species and driven some to extinction. Protecting our remaining biodiversity benefits fundamental biology research, because important biological discoveries can come from the most unexpected species. In this video, discover more about the variety of species that Whitehead Institute researchers use and what they hope to learn from them.

MAKING GREEN DRUGS: TAPPING INTO NATURE WITHOUT TAPPING IT OUT

Whitehead Institute Member Jing-Ke Weng’s lab has developed a system to discover medicines in nature and produce them more sustainably, reducing the negative environmental impacts of pharmaceutical research and production. Read about it here.

AUDIOHELICASE SPECIAL: HOW RESEARCHERS AT WHITEHEAD INSTITUTE ARE BUILDING A MORE SUSTAINABLE FUTURE

Many graduate students and postdoctoral researchers at Whitehead Institute are passionate about how their research could help to tackle climate change and other threats to the environment. To hear from some of these early-career researchers directly, click here.

DESIGNING PLANTS THAT DON’T DECAY

Multiple labs at Whitehead Institute have recently joined forces, along with a lab at the Massachusetts Institute of Technology, in the hopes of developing a method for carbon capture to fight greenhouse gas emissions. Read more here.

BIONOOK

Inviting kids to explore the natural world scientifically is a great way to build a foundation for understanding climate change and making eco-conscious decisions. To learn more about Whitehead Institute’s educational offerings, explore BioNook, the Institute’s online biology resource center for students, parents, and teachers.

November 26, 2020
The bull Y chromosome has evolved to bully its way into gametes
Whitehead Institute
November 18, 2020

In a new study, published Nov. 18 in the journal Genome Research, scientists in the lab of Whitehead Institute Member David Page present the first ever full, high-resolution sequence of the Y chromosome of a Hereford bull. The research, more than a decade in the making, suggests that bulls’ Y chromosomes have evolved dozens of copies of the same genes in a selfish attempt to make more males — a move that is countered in the female-determining X chromosome.

“When you have an X and a Y chromosome, it’s a setup for conflict,” said Page, who is also a professor of biology at the Massachusetts Institute of Technology and investigator with the Howard Hughes Medical Institute. “Seeing this full blown competition between the cattle X and Y means we have to think more deeply about this conflict as a constant and general feature of sex chromosomes in mammals.”

This insight into the forces that govern sex chromosome behavior and evolution will help scientists in Page’s lab study genetic differences between males and females and how they play out in health and disease across every part of the body, Page added.

Of mice, men and cattle 

Sex chromosomes — the X and the Y — evolved from a regular pair of symmetrical chromosomes some 200 million years ago. Those born biologically female have two X chromosomes. Those born biologically male have one X and one Y.

Page’s lab successfully sequenced the human Y chromosome in 2003, and afterwards the researchers wanted to be able to compare the sequence to its counterparts in other animals in order to help understand how they have evolved and diverged over time.

To make these comparisons, researchers in Page’s lab laid out a list of several mammals — including chimps, opossums, and mice — that occupied different branches of the mammalian family tree. One after another, the scientists began sequencing these creatures’ Ys, using a high-resolution sequencing method called SHIMS — short for Single-Haplotype Iterative Mapping and Sequencing — to obtain a level of detail that other techniques, like shotgun sequencing, can’t.

This powerful sequencing technology allowed the researchers to observe a strange peculiarity of Y chromosomes: in some species, nearly all of the genetic material on the Y is made up of sequences of DNA that have been amplified dozens or hundreds of times over — “like a hall of mirrors,” Page said.

In mice, for example, repeats of just a few testis-specific genes make up nearly 98 percent of the Y chromosome. In humans, however, repeats make up only about 45 percent. “We wanted to know if this was just a peculiarity of rodents, or if other Y chromosomes might come close,” Page said.

That’s where the bull came in. “Outside of primates and rodents, the next branch off the mammalian tree includes bull,” said Jennifer Hughes, a researcher in Page’s lab and the first author of the paper. “We didn’t know if the bull’s Y chromosome would look like a mouse Y or a human Y or something else entirely.”

The running of the bull’s (sequencing data) 

It took the Page Lab and collaborators at Baylor College of Medicine’s Human Genome Sequencing Center, the McDonnell Genome Institute at Washington University, Texas A&M University, and other institutions more than a decade to tease apart the complexities of the bull Y chromosome. In fact, it turned out to be the most gene-dense of any Y chromosome ever mapped — largely due to the fact that 96 percent of its genetic material was made up of repetitive sequences.

As in the mouse, most of the bull’s “hall of mirrors” repeats appeared to be expressed in the testis. But the question remained: Why? “What drives it can’t just be purely making more sperm, because that’s just overkill, right?” Hughes said. “You don’t really need hundreds of copies of a gene to accomplish that task.”

The researchers found a clue when they took a closer look at the bovine X chromosome: the female-determining sex chromosome also had a few copies of these testis-specific genes. “We don’t really know the mechanism in the bull, but the thought is that somehow the amplification of these genes in the Y has to do with helping the Y get passed on — and the X copies are amplified to compete against that tendency and help the X,” Hughes said.

A selfish pursuit

This X-Y arms race has been proven to happen in mice: somehow, repetitive genes on the Y chromosome give it an extra edge when it comes to ending up in the sperm during gamete formation. In a 2012 study, researchers knocked out the Y-chromosome repeats. Without the extra genes, more X chromosomes than Ys ended up in sperm cells, and the sex ratio of offspring skewed female. Over years of evolution, the X has developed repeats as well — its own way to get a leg up in the race.

Competition between X and Y chromosomes is selfish, Hughes said, because it’s not a good thing for the species to have a skewed sex ratio. Thus, these alterations benefit only the lucky chromosome that ends up in the fertilized egg. The fact that a selfish — and even detrimental — mechanism would continue for millions of years in disparate branches of the evolutionary tree suggests that these conflicts may be an inevitable side effect of having a pair of asymmetrical sex chromosomes. “These X-Y arms races have probably been around for as long as mammals have been around,” Page said.

Evolutionary theory aside, knowing the mechanisms controlling the sex ratios of cattle could be of practical use in the coming years. “It could be of great interest to breeders, because they would love to be able to manipulate the sex of cattle offspring,” Hughes said. “For example, dairy farmers would prefer more females and meat farmers would prefer more males.”

Right now, the lab is working on leafing out the branches of their Y chromosome evolutionary tree. The bull’s is the seventh sex chromosome to be completely sequenced using the SHIMS method. Hughes, Page and the lab are also eyeing members of other animal groups, including reptiles.

“Our lab is focused on sex differences across the human body, and all of that work really is inspired by lessons that we’ve learned by comparing the Y chromosomes of different animals with our own,” Page said. “It’s like when you go to an art gallery and just sit on a bench and look and feel inspired — these sequences are an infinite source of inspiration in the work we are doing. And we can now add the bull to our gallery.”

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Hughes, J. et al. “Sequence analysis in Bos taurus reveals pervasiveness of X-Y arms races in mammalian lineages.” Genome Research, Nov. 18, 2020. DOI: 10.1101/gr.269902.120

A research tool of a different color
Greta Friar | Whitehead Institute
November 18, 2020

Melanosomes are the organelles, or structures, inside our cells, that produce melanin, the molecule that gives our skin, hair and eyes their color. Melanosomes produce several different forms of melanin, including black/brown coloration and yellow/red coloration, and the many variations in levels at which each coloration can be produced in an individual generate the wide variety of skin, hair, and eye colors in the world.

Many genes that have been associated with skin color encode proteins that are active in melanosomes, but their specific functions are unknown, leaving gaps in researchers’ understanding of the underlying biology of skin color. In order to help researchers get a more detailed understanding of melanosome biology, Whitehead Institute Member David Sabatini’s lab has developed a tool, called MelanoIP, with which researchers can rapidly and specifically isolate melanosomes from the cell and analyze their contents. Using this tool, researchers can uncover the identity of the proteins at work there and explain mechanistically how genetic variation contributes to differences in skin color. In research published in Nature on November 18, Sabatini and graduate student Charles Hank Adelmann unveil MelanoIP and explain how they used it to crack the identity of melanosome protein MFSD12.

MelanoIP is the latest in a series of tools based on a method that Sabatini, who is also a professor of biology at Massachusetts Institute of Technology and an investigator with the Howard Hughes Medical Institute, and collaborators developed to rapidly extract specific organelles from the cell for investigation. Sabatini and former graduate student Walter Chen first developed the method to isolate mitochondria. The process starts with researchers creating a tag that localizes to the organelle type of interest. Then they expose the contents of the whole cell to beads covered in antibodies that latch onto the tags, which pull the organelles with them when they are collected. The lab has since adapted this process to use on lysosomes, the recycling centers of the cell, and peroxisomes, organelles important in several metabolic processes—and now, melanosomes.

The first melanosome protein that Sabatini and Adelmann turned their attention to, MFSD12, was known to be linked to the production of red coloration or pheomelanin. When MFSD12 is suppressed, this leads to darker skin color in humans and mice, because the melanosomes are generating brown/black melanin but not any of the lighter red melanin. However, MFSD12’s exact role was unknown. Using MelanoIP, Adelmann discovered that MFSD12 is required for the import of the amino acid cysteine into melanosomes, which is a necessary component in red melanin synthesis. Adelmann’s research suggests that MFSD12 is itself the transporter, but further work is needed to confirm whether it works alone or in conjunction with other molecules.

One reason that the Sabatini lab picked the melanosome as the next organelle to apply their IP toolkit to is because of its close relation to the lysosome, one of the organelles for which the lab had already built such a tool. This close relation proved relevant in Adelmann’s research on MFSD12, when he discovered that the protein is also required for the transport of cysteine into lysosomes. People with the rare genetic disorder cystinosis are affected by the buildup of cystine, another form of cysteine, in lysosomes. Adelmann found that by inhibiting MFSD12, and preventing cysteine from entering lysosomes, he could reverse the buildup of cystine in cells with the genetic mutation linked to cystinosis, suggesting a potential therapeutic use for MFSD12 inhibitors.

Adelmann is now turning his attention to cracking the identity of more of the proteins active in melanosomes and uncovering more of the biology underlying variation in skin color.

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Written by Greta Friar

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Adelmann, Charles H. et al. “MFSD12 mediates the import of cysteine into melanosomes and lysosomes.” Nature, Nov. 18, 2020. DOI: 10.1038/s41586-020-2937-x

Vaccine Booster

Biologist Jianzhu Chen works to enhance immune response

Mark Wolverton | Spectrum
November 16, 2020

Jianzhu Chen, professor of biology and a member of the Koch Institute for Integrative Cancer Research at MIT, is pursuing a different strategy from most of his colleagues working on SARS-CoV-2, the virus that causes Covid-19. “We focus on the immune system and fundamental mechanisms as well as their application in cancer immunotherapy, vaccine development, and metabolic diseases,” he explains. Rather than trying to develop a specific vaccine, Chen is pursuing vaccine platform technologies that can be used to enhance any vaccine.

This effort is built on Chen’s previous work on dengue fever, a severe tropical disease transmitted by mosquitos. “We have been working to improve a vaccine against dengue virus infection,” he says, “which has this phenomenon called antibody-dependent enhancement,” in which “non-neutralizing” antibodies bind to the virus but do not destroy it. The immune system’s pathogen-eating macrophages then consume these virus-antibody complexes and become infected themselves, making a subsequent infection worse.

Chen’s team has identified vaccine adjuvants, or enhancing agents, that can increase neutralizing (that is, effective) antibodies while reducing non-neutralizing antibody response in mice and nonhuman primates. The team is confident that using a similar strategy against Covid-19 would improve any vaccine’s effectiveness.

Addressing cytokine storm

Chen is also focusing on the dangerous hyperinflammatory response seen in Covid-19: the cytokine storm that can result when the immune system overreacts to infection.

“We have been working on macrophage biology for quite some time,” Chen says. “SARS-CoV-2 infection is a hyperinflammatory response, and macrophages probably play a critical role in that response.”

“We have identified many compounds, including FDA-approved drugs, bioactive compounds, and natural products that can modulate macrophage activity to become anti-inflammatory,” he says. Such macrophage modulation would likely be used in conjunction with other treatments as a therapeutic strategy for already-infected patients.

A promising result from either research project could be used along with a Covid-19 vaccine to enhance immune response while preventing or reducing the severity of any possible reinfection. But it’s too early to tell what might happen. “We don’t have a vaccine yet,” Chen notes. “It’s not clear when we’ll have one. Even when we have one, it’s not clear how well it will work. It could be 95% protection; it could be 50%. Some of them may not confer much protection at all. But even 50% or 60% is a significant number of people.”

Another challenge, Chen acknowledges, is that medical research must move from theory to lab and ultimately into the real world. Vaccines can be designed and modeled on computers but eventually “we have to test them to see if they work as we expect,” he says. “You have to immunize mice or some other animals and then challenge them with SARS-CoV-2 to see whether the vaccine protects the animals from infection or dramatically minimize disease symptoms. These kinds of studies can’t be modeled computationally.”

Chen also hopes that his particular contributions will have benefits beyond the pandemic. “We’re aiming to develop a vaccine platform prototyped on SARS-CoV-2 that can be used for the development of many other vaccines as well, using the most appropriate technologies.” If that happens, science will have dug at least one substantial jewel out of the depths of an unprecedented public health crisis.