Genetic Background and Environment Influence the Effects of Mutations in pykF and Help Reveal Mechanisms Underlying Their Benefit
نویسندگان
چکیده
Genetic Background and Environment Influence the Effects of Mutations in pykF and Help Reveal Mechanisms Underlying Their Benefit Report Title Resolving the relationship between genotypes and their effects remains a central challenge in the study of adaptation. Although parallel mutations, a signature of adaptation, have been observed a lot in natural and lab-evolved populations, it is unknown if they are equally adaptive, or even if they affect similar biological processes to cause phenotypic changes. Using eight independently occurring mutations in pykF identified from a long-term evolution experiment with Escherichia coli, I found the mutations confer similar benefits in the ancestral background, but variable effects in the background in which they were evolved. Differences in mutation × background interactions were found to be driven by different suites of mutations in each genetic background, rather than by different pykF mutations. Through biochemical and physiological studies with the pykF mutations in the ancestor, I found that although the mutations affect enzymes in a range of different ways, the net effect of these changes is to lead to changes in the same biological pathways, and thus to confer similar fitness effects. An adaptive mutation may no longer be beneficial if the given genetic background or environment changes. Relatively few studies, however, have examined the combined effect of genetic and environmental context on fitness effects of a mutation. To do this, I measured fitness effect conferred by one pykF mutation in 23 divergent genetic backgrounds and five environments. I found the environment, genetic background, and interactions between them, all significantly affect fitness of the mutation, which makes it harder to predict evolutionary fate of new mutations. Nevertheless, I found that initial fitness of a progenitor strain can be used to predict contribution of a mutation: a mutation will contribute less when added to fitter progenitors. Genetic Background and Environment Influence the Effects of Mutations in pykF and Help Reveal Mechanisms Underlying Their Benefit
منابع مشابه
Effects of Beneficial Mutations in pykF Gene Vary over Time and across Replicate Populations in a Long-Term Experiment with Bacteria
The fitness effects of mutations can depend on the genetic backgrounds in which they occur and thereby influence future opportunities for evolving populations. In particular, mutations that fix in a population might change the selective benefit of subsequent mutations, giving rise to historical contingency. We examine these effects by focusing on mutations in a key metabolic gene, pykF, that ar...
متن کاملDetection of P 53 gene mutations in exons 5 and 8 in patients of familial breast cancer with PCR-SSCP methode.
Background: Breast cancer is one of the most common cancer of women in the world. Although different genetic alteration has been reported in this malignancy, but P 53 gene mutations has more frequency. P 53 gene is one of the most important suppressor genes and it play a central role in breast cancer and detecting of mutations in this gene would be very helpful in understanding of genetic m...
متن کاملتوالی یابی نسل جدید (NGS) روشی برای شناسایی جهش های ژنتیکی مرتبط با اختلال اسپینابیفیدا
Background and Objective: Spina Bifida (SB) is a congenital malformation and is a result of the failure of the closure and failure of the neural tube. The causes and mechanisms of genetic involvement involved in the onset of SB are still ambiguous. The present study addresses the genetic variation in SB disease using Next Generation Sequencing (NGS) as a powerful molecular tool for comprehensiv...
متن کاملجهش های ژنتیکی جدید در ژن های اصلی سرطان پستان (BRCA1/BRCA2) در زنان ایرانی مبتلا به سرطان پستان زودرس
Background: Breast cancer is the most common female malignancy and the main cause of death in mid-aged women. Genetic germ line mutations in BRCAI/BRCA2 in Iranian women with breast or ovarian cancer have not been yet reported. Materials and methods: Clinical data, family history and blood samples were obtained from 83 females aged less than 45 years with primary breast cancer in order to su...
متن کاملNF1 Mutations Analysis Using Whole Exome Sequencing Technique in 11 Unrelated Iranian Families with Neurofibromatosis Type 1
Background Neurofibromatosis is an autosomal dominant disease. It affects one in 2,700 to 3,300 people. The main gene mutated in the disease is a tumor suppressor protein called neurofibromin. There are several categories, the most important of which is divided into two types of type I and type 2 neurofibromatosis. Here, we aimed to identify th...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
عنوان ژورنال:
دوره شماره
صفحات -
تاریخ انتشار 2016