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Tuesday, October 18, 2011

Facts and Figures on Rural Women



POVERTY

  • Countries with the highest levels of hunger also have very high levels of gender inequality (2009 Global Hunger Index. The Challenge of Hunger: Focus on Financial Crisis and Gender Inequality. IFPRI Issue Brief 62.)
  • Gender inequality is a major cause and effect of hunger and poverty: it is estimated that 60 percent of chronically hungry people are women and girls (WFP Gender Policy and Strategy).
  • In the context of Latin America 110 women aged 20 to 59 are living in poor rural households for every 100 men in Colombia and 114 women for every 100 men in Chile. In sub-Saharan Africa (Cameroon, Malawi, Namibia, Rwanda and Zimbabwe) there are more than 120 women aged 20 to 59 living in poor households for every 100 men (UN Women Progress report 2011).

AGRICULTURE

  • Estimates suggest that if women had the same access to productive resources as men, they could increase yields on their farms by 20–30 percent, lifting 100-150 million out of hunger (FAO (2011). The State of Food and Agriculture: Women in Agriculture, Closing the Gender Gap for Development, Rome).
  • Equal access to resources will raise total agricultural output in developing countries by 2.5–4 percent, thereby contributing to both food security and economic growth (FAO (2011). The State of Food and Agriculture: Women in Agriculture, Closing the Gender Gap for Development’, Rome)
  • The OECD estimates from recent years show that only 5 percent of aid directed to the agricultural sector specifically focused on gender equality. (OECD, The Development Co-operation Report 2011)
  • Women constitute half of the agricultural labour force in least developed countries (FAO, The Role of Women in Agriculture).

LAND RIGHTS

  • For those developing countries for which data are available, only between 10 and 20 percent of all land holders are women FAO (2011). The State of Food and Agriculture: Women in Agriculture, Closing the Gender Gap for Development’, Rome).

LABOUR FORCE

  • In most countries women in rural areas who work for wages are more likely than men to hold seasonal, part-time and low-wage jobs and women receive lower wages for the same work (FAO (2011). The State of Food and Agriculture: Women in Agriculture, Closing the Gender Gap for Development’, Rome).

ACCESS TO CREDIT

  • The share of female smallholder farmers who can access credit is 5-10 percentage points lower than for male smallholders.  (FAO (2011). The State of Food and Agriculture: Women in Agriculture, Closing the Gender Gap for Development’, Rome)
  • In rural sub-Saharan Africa, women in smallholder agriculture access less than 10 percent of available credit (UN (2011). Report of the Secretary-General on Ten-year appraisal and review of the implementation of the Brussels Programme of Action for the Least Developed Countries for the Decade 2001-2010, A/66/66.)

HEALTH

  • Only one third of rural women receive prenatal care compared to 50 per cent in developing regions as a whole. (United Nations, The Millennium Development Goals Report 2010 and 2011 (New York, 2010 and 2011), available from www.un.org/millenniumgoals/reports.shtml .)

INFRASTRUCTURE AND ICTS

  • In LDCs, the electrification rate ranges from below 10 to 40 per cent and the percentage of population with improved access to drinking water in rural areas ranges from 9 to 97 per cent with significant disparities between urban and rural areas. People in LDCs rely on open fires and traditional cooking stoves (e.g. wood, crop waste and charcoal) to earn a living and feed their families. Women walk long distances every day to collect fuels (and water) (UNIDO (2011). Contribution to the LDC IV Conference on Energy Access).
  • Access to new technology is crucial in maintaining and improving agricultural productivity. Gender gaps exist for a wide range of agricultural technologies, including machines and tools, improved plant varieties and animal breeds, fertilizers, pest control measures and management techniques. Labour saving and productivity enhancing technologies can also help reduce women’s time poverty.

RELATED LINKS

New research links common RNA modification to obesity








An international research team has discovered that a pervasive human RNA modification provides the physiological underpinning of the genetic regulatory process that contributes to obesity and type II diabetes.
European researchers showed in 2007 that the FTO gene was the major gene associated with obesity and type 2 diabetes, but the details of its physiological and cellular functioning remained unknown.
Now, a team led by University of Chicago chemistry professor Chuan He has demonstrated experimentally the importance of a reversible RNA modification process mediated by the FTO protein upon biological regulation. He and 10 co-authors from Chicago, China and England published the details of their finding in the Oct. 16 advance online edition of Nature Chemical Biology.
Caption: Chuan He, professor in chemistry at the University of Chicago, works in his laboratory in the Gordon Center for Integrative Science. He led an international research team that has experimentally demonstrated that RNA modification wields greater genetic influence than previously suspected. Credit: Lloyd DeGrane
He and his colleagues have shown, for the first time, the existence of the reversible RNA modification process — called methylation — and that it potentially impacts protein expression and function through its action on a common RNA base: adenosine. The process is reversible because it can involve the addition or removal of a methyl group from adenosine. The team found that the FTO protein mediates cellular removal of the methyl group.
“An improved understanding of the normal functions of FTO, as exemplified by this work, could aid the development of novel anti-obesity therapies,” said Stephen O’Rahilly, professor of clinical biochemistry and director of the Metabolic Research Laboratories at the University of Cambridge. O’Rahilly, a leading researcher in obesity and metabolic disease who also has studied FTO, was not directly involved in He’s project.
“Variants around the FTO gene have consistently been associated with human obesity and artificial manipulation of the fto gene in mice clearly demonstrates that FTO plays a crucial role in the regulation of body weight,” O’Rahilly explained. “However, the development of a deeper understanding of the normal biological role of FTO has been challenging.”
Scientists already had demonstrated that FTO removes methyl groups from nucleic acids, but only on one rare type of DNA or RNA methylation. The new research from He and his colleagues shows that FTO also acts on the common messenger RNA modification called N6-methyladenosine, O’Rahilly said.
The paper arose from He’s investigations of the AlkB family of proteins that act on nucleic acids. Based on this work, He and his collaborators proved that human cells exhibit reversible methylation of RNA bases, which significantly impact critical life processes.
Important but mysterious
Every human messenger RNA carries on average three to six methylations on adenosine. Scientists knew these methylations were extremely important but their function remained a mystery, He said. “For the first time, we show that these methylations are reversible and play a key role in human energy homeostasis,” the process by which the body maintains a complex biochemical dynamic equilibrium.
The modification of N6-methyladenosine in messenger RNA is pervasive throughout the mammal kingdom and many other organisms. Despite its abundance, this modification’s exact functional role remains unknown, He said. But his team’s discovery strongly indicates that the modification has major roles in messenger RNA metabolism.
The finding may open a new research field — RNA epigenetics — for delving into the realm of biological regulatory processes, He said. The epigenetics of DNA and histones (proteins that package DNA in human cells) have become well-explored topics on the frontiers of biological research over the last 10 to 20 years. “It is safe to say 50 percent of biologists work on subjects related to epigenetics one way or another,” He said.
DNA (deoxyribonucleic acid) for decades has reigned as king over biological research on epigenetics of nucleic acids, as He noted in the December 2010 issue of Nature Chemical Biology. RNA (ribonucleic acid) modification was regarded more as a vassal that merely fine-tunes gene expression and regulation, until this recent discovery, which confirms the speculation by He and others that RNA modification has secretly wielded a far greater genetic influence than anyone had previously suspected. That’s why, as He wrote last year, “reversible RNA modification might represent another realm for biological regulation in the form of ‘RNA epigenetics.’”
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Citations: “N6-Methyladenosine in nuclear RNA is a major substrate of the obesity-associated FTO,” by Guifang Jia, Ye Fu, Xu Zhao, Qing Dai, Guanqun Zheng, Ying Yang, Chengqi Yi, Tomas Lindahl, Tao Pan, Yun-Gui Yang and Chuan He, Nature Chemical Biology, advance online publication Oct. 16, 2011.

Faulty molecular switch can cause infertility or miscarriage





Scientists have discovered an enzyme that acts as a ‘fertility switch’, in a study published in Nature Medicine today. High levels of the protein are associated with infertility, while low levels make a woman more likely to have a miscarriage, the research has shown.
The findings have implications for the treatment of infertility and recurrent miscarriage and could also lead to new contraceptives. Around one in six women have difficulty getting pregnant and one in 100 women trying to conceive have recurrent miscarriages, defined as the loss of three or more consecutive pregnancies.
Researchers from Imperial College London looked at tissue samples from the womb lining, donated by 106 women who were being treated at Imperial College Healthcare NHS Trust either for unexplained infertility or for recurrent pregnancy loss.
The women with unexplained infertility had been trying to get pregnant for two years or more and the most common reasons for infertility had been ruled out. The researchers discovered that the womb lining in these women had high levels of the enzyme SGK1. Conversely, the women suffering from recurrent pregnancy loss had low levels of SGK1.
The team found further evidence of SGK1′s importance in experiments using mouse models. Levels of SGK1 in the womb lining decline during the fertile window in mice. When the researchers implanted extra copies of the SGK1 gene into the womb lining, the mice were unable to get pregnant, suggesting that a fall in SGK1 levels is essential for making the uterus receptive to embryos.
The research at the Institute of Reproductive and Developmental Biology (IRDB) at Imperial College London was led by Professor Jan Brosens, who is now based at the University of Warwick. “Our experiments on mice suggest that a temporary loss of SGK1 during the fertile window is essential for pregnancy, but human tissue samples show that they remain high in some women who have trouble getting pregnant,” he said. “I can envisage that in the future, we might treat the womb lining by flushing it with drugs that block SGK1 before women undergo IVF. Another potential application is that increasing SGK1 levels might be used as a new method of contraception.”
Any infertility treatment that blocks SGK1 would have to have a short-lived effect, as low levels of the protein after conception seem to be linked to miscarriage. When the researchers blocked the gene that codes for SGK1 in mice, the mice had no problem getting pregnant. However, they had smaller litters and showed signs of bleeding in the uterus, suggesting that lack of SGK1 made miscarriage more likely.
After an embryo is implanted, the lining of the uterus develops into a specialised structure called the decidua, and this process can be made to occur when cells from the uterus are cultured in the lab. Cultured cells from women who had had three or more consecutive miscarriages had significantly lower levels of SGK1 compared to cells from controls.
Blocking the SGK1 gene, both in pregnant mice and in human cell cultures, impaired the cells’ ability to protect themselves against oxidative stress, a condition in which there is an excess of reactive chemicals inside cells.
“We found that low levels of SGK1 make the womb lining vulnerable to cellular stress, which might explain why low SGK1 was more common in women who have had recurrent miscarriage,” said Madhuri Salker, the study’s first author, Institute of Reproductive and Developmental Biology (IRDB) at Imperial College London. “In the future, we might take biopsies of the womb lining to identify abnormalities that might give them a higher risk of pregnancy complications, so that we can start treating them before they get pregnant.”