miR-9a Minimizes the Phenotypic Impact of Genomic Diversity by Buffering a Transcription Factor

نویسندگان

  • Justin J. Cassidy
  • Aashish R. Jha
  • Diana M. Posadas
  • Ritika Giri
  • Koen J.T. Venken
  • Jingran Ji
  • Hongmei Jiang
  • Hugo J. Bellen
  • Kevin P. White
  • Richard W. Carthew
چکیده

Gene expression has to withstand stochastic, environmental, and genomic perturbations. For example, in the latter case, 0.5%-1% of the human genome is typically variable between any two unrelated individuals. Such diversity might create problematic variability in the activity of gene regulatory networks and, ultimately, in cell behaviors. Using multigenerational selection experiments, we find that for the Drosophila proneural network, the effect of genomic diversity is dampened by miR-9a-mediated regulation of senseless expression. Reducing miR-9a regulation of the Senseless transcription factor frees the genomic landscape to exert greater phenotypic influence. Whole-genome sequencing identified genomic loci that potentially exert such effects. A larger set of sequence variants, including variants within proneural network genes, exhibits these characteristics when miR-9a concentration is reduced. These findings reveal that microRNA-target interactions may be a key mechanism by which the impact of genomic diversity on cell behavior is dampened.

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

microRNAs suppress cellular phenotypic heterogeneity

microRNAs are small noncoding RNAs that reduce protein output from complementary target mRNA transcripts. They are a conserved family of gene regulators in multicellular organisms, targeting much of the transcriptome. This pervasiveness is at odds with their generally modest repressive capacity, and suggests that microRNAs might not be cellular decision makers; rather they might ensure the stab...

متن کامل

Mycobacterium avium subsp. paratuberculosis induces differential cytosine methylation at miR-21 transcription start site region

Mycobacterium aviumsubspecies paratuberculosis (MAP), as an obligate intracellular bacterium, causes paratuberculosis (Johne’s disease) in ruminants. Plus, MAP has consistently been isolated from Crohn’s disease (CD) lesions in humans; a notion implying possible direct causative ...

متن کامل

Differential Masking of Natural Genetic Variation by miR-9a in Drosophila.

Genetic variation is prevalent among individuals of the same species and yet the potential effects of genetic variation on developmental outcomes are frequently suppressed. Understanding the mechanisms that are responsible for this suppression is an important goal. Previously, we found that the microRNA miR-9a mitigates the impact of natural genetic variants that promote the development of scut...

متن کامل

تاثیر دویدن اجباری هوازی کوتاه مدت بر بیان ژن‌های miR-124 وRE1-Silencing Transcription Factor در هیپوکامپ موش‌های صحرایی نر بالغ

Background and Objective: Transcription factors (TF) and microRNAs, are the largest families of transacting gene regulatory molecules in multicellular organisms. Our goal was to examine the effect of aerobic running on the expression of miR-124 and RE1-silencing TF in the hippocampus of adult male Wistar rats. Materials and Methods: A total of twelve 8-week-old adult male Wistar rats with a mea...

متن کامل

Insights on the Functional Impact of MicroRNAs Present in Autism-Associated Copy Number Variants

Autism spectrum disorder is a complex neurodevelopmental disorder that appears during the first three years of infancy and lasts throughout a person's life. Recently a large category of genomic structural variants, denoted as copy number variants (CNVs), were established to be a major contributor of the pathophysiology of autism. To date almost all studies have focussed only on the genes presen...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

عنوان ژورنال:
  • Cell

دوره 155  شماره 

صفحات  -

تاریخ انتشار 2013